Item | Value |
---|---|
geneid | 164045 |
ensemblid | ENSG00000162669.16 |
hgncid | 20193 |
symbol | HFM1 |
name | helicase for meiosis 1 |
refseq_nuc | NM_001017975.6 |
refseq_prot | NP_001017975.5 |
ensembl_nuc | ENST00000370425.8 |
ensembl_prot | ENSP00000359454.3 |
mane_status | MANE Select |
chr | chr1 |
start | 91260766 |
end | 91404837 |
strand | - |
ver | v1.2 |
region | chr1:91260766-91404837 |
region5000 | chr1:91255766-91409837 |
regionname0 | HFM1_chr1_91260766_91404837 |
regionname5000 | HFM1_chr1_91255766_91409837 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1435 | 317 | 61 | 53 | 155 | 8 | 39 | 127 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0002 | 0/0 | 1435 | 30 | 15 | 9 | 0 | 4 | 2 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0003 | 0/0 | 1435 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0004 | 0/0 | 1435 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MPKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0005 | 0/0 | 1435 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0006 | 0/0 | 1435 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0007 | 0/0 | 1435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0008 | 0/0 | 1435 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
a0009 | 0/1 | 1435 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | MLKSN others(1430): Show |
chr1 | 91255766 | 91409837 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4305 | 232 | 42 | 44 | 114 | 6 | 26 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0002 | 0/0 | 4305 | 48 | 6 | 6 | 30 | 1 | 5 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0004 | 0/0 | 4305 | 22 | 12 | 3 | 0 | 0 | 7 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0005 | 0/0 | 4305 | 8 | 0 | 0 | 8 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0007 | 0/0 | 4305 | 3 | 0 | 0 | 3 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0015 | 1/0 | 4305 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0016 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0017 | 0/0 | 4305 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0001c0019 | 0/0 | 4305 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0002c0003 | 0/0 | 4305 | 30 | 15 | 9 | 0 | 4 | 2 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0003c0009 | 0/0 | 4305 | 2 | 1 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0003c0012 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0003c0013 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0004c0008 | 0/0 | 4305 | 2 | 2 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCC others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0004c0011 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCC others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0005c0006 | 0/0 | 4305 | 3 | 0 | 0 | 3 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0006c0010 | 0/0 | 4305 | 2 | 2 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0007c0020 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0008c0018 | 0/0 | 4305 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 | ||
a0009c0014 | 0/1 | 4305 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | ATGCT others(4300): Show |
chr1 | 91255766 | 91409837 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4899 | 230 | 42 | 43 | 113 | 6 | 26 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0001t0002 | 0/0 | 4899 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0001t0004 | 0/0 | 4899 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0002t0001 | 0/0 | 4899 | 47 | 5 | 6 | 30 | 1 | 5 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0002t0005 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0004t0001 | 0/0 | 4899 | 22 | 12 | 3 | 0 | 0 | 7 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0005t0002 | 0/0 | 4899 | 8 | 0 | 0 | 8 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0007t0001 | 0/0 | 4899 | 3 | 0 | 0 | 3 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0015t0001 | 1/0 | 4899 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0016t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0017t0001 | 0/0 | 4899 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0001c0019t0001 | 0/0 | 4899 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0002c0003t0001 | 0/0 | 4899 | 29 | 15 | 8 | 0 | 4 | 2 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0002c0003t0003 | 0/0 | 4899 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0003c0009t0001 | 0/0 | 4899 | 2 | 1 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0003c0012t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0003c0013t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0004c0008t0001 | 0/0 | 4899 | 2 | 2 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0004c0011t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0005c0006t0001 | 0/0 | 4899 | 3 | 0 | 0 | 3 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0006c0010t0001 | 0/0 | 4899 | 2 | 2 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0007c0020t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0008c0018t0001 | 0/0 | 4899 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
a0009c0014t0003 | 0/1 | 4899 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | AAATC others(4894): Show |
chr1 | 91255766 | 91409837 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0002t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0005t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0007t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0007t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0015t0001g0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0016t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0017t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0001c0019t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0002c0003t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0003c0009t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0003c0009t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0003c0012t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0003c0013t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0004c0008t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0004c0008t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0004c0011t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0005c0006t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0005c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0005c0006t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0006c0010t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0006c0010t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0007c0020t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0008c0018t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
a0009c0014t0003g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00280 | hp1 | a0002 | c0003 | t0001 | g0178 | EUR | FIN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00280 | hp2 | a0001 | c0019 | t0001 | g0134 | EUR | FIN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0041 | EUR | FIN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00609 | hp1 | a0001 | c0007 | t0001 | g0188 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0324 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01069 | hp2 | a0002 | c0003 | t0001 | g0329 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01070 | hp2 | a0001 | c0004 | t0001 | g0156 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0328 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0174 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0327 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0341 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01169 | hp2 | a0002 | c0003 | t0001 | g0348 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01192 | hp1 | a0002 | c0003 | t0003 | g0347 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01258 | hp2 | a0002 | c0003 | t0001 | g0340 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0003 | EUR | IBS | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0330 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01884 | hp2 | a0001 | c0002 | t0005 | g0052 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0161 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0339 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02083 | hp2 | a0001 | c0005 | t0002 | g0148 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02135 | hp2 | a0001 | c0005 | t0002 | g0146 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0158 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0332 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02280 | hp1 | a0007 | c0020 | t0001 | g0054 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02280 | hp2 | a0003 | c0009 | t0001 | g0197 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02523 | hp2 | a0001 | c0005 | t0002 | g0145 | EAS | KHV | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02572 | hp1 | a0003 | c0013 | t0001 | g0143 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0322 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02602 | hp1 | a0001 | c0004 | t0001 | g0175 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0331 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0346 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02717 | hp2 | a0006 | c0010 | t0001 | g0243 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02738 | hp2 | a0001 | c0004 | t0001 | g0173 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02886 | hp2 | a0001 | c0016 | t0001 | g0141 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02895 | hp2 | a0002 | c0003 | t0001 | g0323 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0321 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02922 | hp2 | a0006 | c0010 | t0001 | g0244 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02965 | hp1 | a0004 | c0011 | t0001 | g0152 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0167 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0176 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0344 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0163 | AFR | GWD | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0343 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03139 | hp1 | a0001 | c0004 | t0001 | g0169 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03195 | hp1 | a0002 | c0003 | t0001 | g0325 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0164 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03490 | hp1 | a0001 | c0004 | t0001 | g0157 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0336 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0171 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0172 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0170 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0160 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0338 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0355 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04115 | hp2 | a0003 | c0009 | t0001 | g0345 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | BEB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18522 | hp1 | a0002 | c0003 | t0001 | g0335 | AFR | YRI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0166 | AFR | YRI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18943 | hp2 | a0005 | c0006 | t0001 | g0189 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18953 | hp2 | a0001 | c0005 | t0002 | g0150 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18977 | hp2 | a0001 | c0005 | t0002 | g0151 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18981 | hp2 | a0005 | c0006 | t0001 | g0192 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18987 | hp1 | a0001 | c0007 | t0001 | g0193 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18990 | hp1 | a0001 | c0007 | t0001 | g0190 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19006 | hp2 | a0001 | c0005 | t0002 | g0144 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0155 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19054 | hp1 | a0001 | c0005 | t0002 | g0147 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19077 | hp1 | a0005 | c0006 | t0001 | g0191 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19085 | hp1 | a0001 | c0005 | t0002 | g0149 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19240 | hp1 | a0004 | c0008 | t0001 | g0319 | AFR | YRI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0326 | AFR | ASW | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0165 | AFR | ASW | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0342 | EUR | TSI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20805 | hp2 | a0002 | c0003 | t0001 | g0337 | EUR | TSI | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20905 | hp1 | a0001 | c0017 | t0001 | g0351 | SAS | GIH | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | GIH | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01123 | hp1 | a0001 | c0004 | t0001 | g0159 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | CLM | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0334 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03471 | hp1 | a0003 | c0012 | t0001 | g0142 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | USA | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
HG06807 | hp2 | a0002 | c0003 | t0001 | g0333 | AFR | USA | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0168 | AFR | USA | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA21309 | hp1 | a0008 | c0018 | t0001 | g0253 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
NA21309 | hp2 | a0004 | c0008 | t0001 | g0318 | AFR | LWK | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
homoSapiens | chm13v2 | a0009 | c0014 | t0003 | g0352 | REF | REF | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
homoSapiens | grch38p0 | a0001 | c0015 | t0001 | g0006 | REF | REF | HFM1_chr1_91255766_91409837 | HFM1 | chr1 | 91255766 | 91409837 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:91276984 | C | T | 1 | a0005 | 3 | NA18943.hp2 NA18981.hp2 NA19077.hp1 |
missense_variant&splice_region_variant | MODERATE | c.3470G>A | p.Cys1157Tyr | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 31/39 | 3537/4899 | 3470/4308 | 1157/1435 | chr1 | 91276984 | |||
chr1:91316474 | T | C | 1 | a0002 | 30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
missense_variant&splice_region_variant | MODERATE | c.2815A>G | p.Ile939Val | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 26/39 | 2882/4899 | 2815/4308 | 939/1435 | chr1 | 91316474 | |||
chr1:91375392 | C | A | 1 | a0006 | 2 | HG02717.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.1651G>T | p.Ala551Ser | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/39 | 1718/4899 | 1651/4308 | 551/1435 | chr1 | 91375392 | |||
chr1:91378069 | T | C | 1 | a0008 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1351A>G | p.Met451Val | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/39 | 1418/4899 | 1351/4308 | 451/1435 | chr1 | 91378069 | |||
chr1:91380221 | T | A | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.889A>T | p.Arg297Trp | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/39 | 956/4899 | 889/4308 | 297/1435 | chr1 | 91380221 | |||
chr1:91394244 | A | G | 2 | a0002 a0003 |
34 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(31): Show |
missense_variant | MODERATE | c.343T>C | p.Ser115Pro | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/39 | 410/4899 | 343/4308 | 115/1435 | chr1 | 91394244 | |||
chr1:91401078 | A | G | 1 | a0004 | 3 | HG02965.hp1 NA19240.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.5T>C | p.Leu2Pro | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/39 | 72/4899 | 5/4308 | 2/1435 | chr1 | 91401078 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:91273713 | T | C | 1 | a0004c0008 | 2 | NA19240.hp1 NA21309.hp2 |
splice_region_variant&synonymous_variant | LOW | c.3771A>G | p.Lys1257Lys | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/39 | 3838/4899 | 3771/4308 | 1257/1435 | chr1 | 91273713 | |||
chr1:91315856 | T | G | 12 | a0001c0001 a0001c0004 a0001c0005 others(9): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
synonymous_variant | LOW | c.3099A>C | p.Ile1033Ile | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/39 | 3166/4899 | 3099/4308 | 1033/1435 | chr1 | 91315856 | |||
chr1:91316454 | G | A | 2 | a0001c0002 a0007c0020 |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
synonymous_variant | LOW | c.2835C>T | p.Ile945Ile | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 26/39 | 2902/4899 | 2835/4308 | 945/1435 | chr1 | 91316454 | |||
chr1:91319090 | G | A | 2 | a0001c0007 a0005c0006 |
6 | HG00609.hp1 NA18943.hp2 NA18981.hp2 others(3): Show |
synonymous_variant | LOW | c.2800C>T | p.Leu934Leu | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/39 | 2867/4899 | 2800/4308 | 934/1435 | chr1 | 91319090 | |||
chr1:91319330 | G | A | 6 | a0001c0002 a0001c0016 a0002c0003 others(3): Show |
83 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(80): Show |
synonymous_variant | LOW | c.2643C>T | p.Thr881Thr | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 24/39 | 2710/4899 | 2643/4308 | 881/1435 | chr1 | 91319330 | |||
chr1:91324684 | T | C | 1 | a0001c0017 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.2418A>G | p.Leu806Leu | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/39 | 2485/4899 | 2418/4308 | 806/1435 | chr1 | 91324684 | |||
chr1:91351617 | G | T | 1 | a0001c0005 | 8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
synonymous_variant | LOW | c.2004C>A | p.Ile668Ile | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 17/39 | 2071/4899 | 2004/4308 | 668/1435 | chr1 | 91351617 | |||
chr1:91375557 | T | C | 1 | a0004c0008 | 2 | NA19240.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.1566A>G | p.Gln522Gln | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 12/39 | 1633/4899 | 1566/4308 | 522/1435 | chr1 | 91375557 | |||
chr1:91375572 | A | T | 1 | a0003c0012 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1551T>A | p.Ile517Ile | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 12/39 | 1618/4899 | 1551/4308 | 517/1435 | chr1 | 91375572 | |||
chr1:91380177 | T | C | 1 | a0001c0019 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.933A>G | p.Val311Val | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/39 | 1000/4899 | 933/4308 | 311/1435 | chr1 | 91380177 | |||
chr1:91385636 | G | A | 1 | a0001c0004 | 22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
synonymous_variant | LOW | c.693C>T | p.Ile231Ile | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/39 | 760/4899 | 693/4308 | 231/1435 | chr1 | 91385636 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:91260982 | G | C | 1 | a0001c0002t0005 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 39/39 | 308 | chr1 | 91260982 | ||||||
chr1:91261122 | G | A | 1 | a0002c0003t0003 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 39/39 | 168 | chr1 | 91261122 | ||||||
chr1:91261193 | C | T | 1 | a0001c0001t0004 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 39/39 | 97 | chr1 | 91261193 | ||||||
chr1:91261194 | G | A | 2 | a0001c0001t0002 a0001c0005t0002 |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 39/39 | 96 | chr1 | 91261194 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:91261663 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4239-304G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 38/38 | chr1 | 91261663 | |||||||
chr1:91261747 | A | G | 2 | a0001c0007t0001g0188 a0001c0007t0001g0190 |
2 | HG00609.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.4239-388T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 38/38 | chr1 | 91261747 | |||||||
chr1:91262009 | T | C | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 |
3 | HG02109.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4238+232A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 38/38 | chr1 | 91262009 | |||||||
chr1:91262224 | C | G | 28 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(25): Show |
28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.4238+17G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 38/38 | chr1 | 91262224 | |||||||
chr1:91263296 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3975-704A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263296 | |||||||
chr1:91263589 | A | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3975-997T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263589 | |||||||
chr1:91263590 | T | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0002c0003t0001g0321 |
3 | HG02922.hp1 NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3975-998A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263590 | |||||||
chr1:91263591 | T | A | 1 | a0002c0003t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3975-999A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263591 | |||||||
chr1:91263620 | G | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3975-1028C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263620 | |||||||
chr1:91263733 | A | G | 28 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(25): Show |
28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3975-1141T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263733 | |||||||
chr1:91263888 | A | G | 81 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(78): Show |
82 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.3975-1296T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263888 | |||||||
chr1:91263890 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3975-1298A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91263890 | |||||||
chr1:91264149 | T | A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3975-1557A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264149 | |||||||
chr1:91264174 | G | A | 1 | a0001c0002t0001g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3975-1582C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264174 | |||||||
chr1:91264359 | G | GTTTTTTT others(7): Show |
1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3974+1657_3974+165 others(18): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264359 | |||||||
chr1:91264359 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3974+1657_3974+165 others(28): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264359 | |||||||
chr1:91264361 | A | AT | 73 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0063 others(70): Show |
74 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3974+1655dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATT | 31 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0066 others(28): Show |
32 | HG00323.hp1 HG00544.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.3974+1654_3974+165 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0259 a0001c0001t0001g0262 others(11): Show |
14 | HG00558.hp2 HG00673.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3974+1649_3974+165 others(11): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(1): Show |
11 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG00544.hp2 HG01167.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.3974+1648_3974+165 others(12): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0121 a0001c0001t0001g0205 a0001c0001t0001g0270 others(1): Show |
4 | HG03098.hp2 HG03710.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.3974+1646_3974+165 others(14): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3974+1645_3974+165 others(15): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0306 a0001c0004t0001g0164 a0001c0004t0001g0167 |
3 | HG02965.hp2 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3974+1644_3974+165 others(16): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0202 a0002c0003t0001g0323 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3974+1643_3974+165 others(17): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0203 a0002c0003t0001g0321 a0002c0003t0001g0322 |
3 | HG02572.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3974+1642_3974+165 others(18): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0285 a0001c0004t0001g0169 a0002c0003t0001g0335 others(1): Show |
4 | HG03139.hp1 HG03471.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3974+1641_3974+165 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(9): Show |
9 | a0001c0001t0001g0260 a0001c0001t0001g0284 a0001c0001t0001g0307 others(6): Show |
9 | HG01884.hp1 HG01993.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3974+1640_3974+165 others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(10): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0058 others(18): Show |
22 | HG01106.hp2 HG02258.hp1 HG02273.hp2 others(19): Show |
intron_variant | MODIFIER | c.3974+1639_3974+165 others(21): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(11): Show |
20 | a0001c0001t0001g0057 a0001c0001t0001g0136 a0001c0001t0001g0195 others(17): Show |
20 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.3974+1638_3974+165 others(22): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(12): Show |
18 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0211 others(15): Show |
18 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.3974+1637_3974+165 others(23): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(13): Show |
11 | a0001c0001t0001g0209 a0001c0001t0001g0226 a0001c0001t0001g0245 others(8): Show |
11 | HG01071.hp1 HG01071.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3974+1636_3974+165 others(24): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(14): Show |
7 | a0001c0001t0001g0206 a0001c0001t0001g0215 a0001c0001t0001g0225 others(4): Show |
7 | HG02970.hp1 HG03516.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.3974+1635_3974+165 others(25): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(15): Show |
9 | a0001c0001t0001g0062 a0001c0001t0001g0194 a0001c0001t0001g0292 others(6): Show |
9 | HG01258.hp2 HG01943.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3974+1634_3974+165 others(26): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(16): Show |
4 | a0001c0001t0001g0204 a0001c0001t0001g0223 a0001c0001t0001g0230 others(1): Show |
4 | HG00735.hp2 HG03239.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.3974+1633_3974+165 others(27): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(17): Show |
1 | a0008c0018t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3974+1632_3974+165 others(28): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(18): Show |
2 | a0001c0001t0001g0288 a0002c0003t0001g0348 |
2 | HG01169.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.3974+1631_3974+165 others(29): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(19): Show |
2 | a0001c0001t0001g0208 a0002c0003t0001g0327 |
2 | HG01081.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3974+1630_3974+165 others(30): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(20): Show |
1 | a0006c0010t0001g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3974+1629_3974+165 others(31): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | ATTTTTTT others(25): Show |
1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3974+1655_3974+165 others(36): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | A | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0316 |
2 | HG02109.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3974+1656T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | AT | A | 11 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.3974+1655delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | ATTTTT | A | 15 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0181 others(12): Show |
15 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3974+1651_3974+165 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3974+1646_3974+165 others(14): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3974+1645_3974+165 others(15): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | ATTTTTTT others(6): Show |
A | 3 | a0001c0001t0001g0201 a0001c0019t0001g0134 a0003c0009t0001g0345 |
3 | HG00280.hp2 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3974+1643_3974+165 others(17): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264361 | ATTTTTTT others(8): Show |
A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3974+1641_3974+165 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264361 | |||||||
chr1:91264376 | T | TTTTTTTT others(12): Show |
1 | a0006c0010t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3974+1640_3974+164 others(23): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264376 | |||||||
chr1:91264492 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3974+1525G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264492 | |||||||
chr1:91264498 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3974+1519C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264498 | |||||||
chr1:91264522 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0353 |
2 | HG00642.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.3974+1495C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264522 | |||||||
chr1:91264653 | G | T | 2 | a0002c0003t0001g0336 a0002c0003t0001g0338 |
2 | HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.3974+1364C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264653 | |||||||
chr1:91264737 | T | C | 129 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(126): Show |
130 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.3974+1280A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91264737 | |||||||
chr1:91265020 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3974+997T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265020 | |||||||
chr1:91265041 | C | T | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3974+976G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265041 | |||||||
chr1:91265059 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3974+958G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265059 | |||||||
chr1:91265249 | C | T | 81 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(78): Show |
82 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.3974+768G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265249 | |||||||
chr1:91265387 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3974+630A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265387 | |||||||
chr1:91265389 | A | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3974+628T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265389 | |||||||
chr1:91265588 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(82): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.3974+429C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265588 | |||||||
chr1:91265869 | T | G | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3974+148A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265869 | |||||||
chr1:91265956 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3974+61G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 36/38 | chr1 | 91265956 | |||||||
chr1:91266111 | T | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01891.hp1 HG02630.hp1 |
splice_region_variant&intron_variant | LOW | c.3884-4A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91266111 | |||||||
chr1:91266199 | T | C | 50 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(47): Show |
51 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.3884-92A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91266199 | |||||||
chr1:91266610 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3884-503A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91266610 | |||||||
chr1:91267019 | A | C | 1 | a0001c0004t0001g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3883+726T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267019 | |||||||
chr1:91267249 | T | G | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3883+496A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267249 | |||||||
chr1:91267320 | C | G | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3883+425G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267320 | |||||||
chr1:91267459 | T | G | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3883+286A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267459 | |||||||
chr1:91267522 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3883+223A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267522 | |||||||
chr1:91267555 | T | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0196 |
3 | HG01257.hp2 HG01258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3883+190A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267555 | |||||||
chr1:91267559 | TA | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3883+185delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267559 | |||||||
chr1:91267563 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3883+182C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 35/38 | chr1 | 91267563 | |||||||
chr1:91267870 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3773-15A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91267870 | |||||||
chr1:91268014 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3773-159A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91268014 | |||||||
chr1:91268127 | T | G | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
22 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.3773-272A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91268127 | |||||||
chr1:91268252 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3773-397A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91268252 | |||||||
chr1:91268437 | T | A | 5 | a0001c0001t0001g0257 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG01433.hp2 HG02300.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3773-582A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91268437 | |||||||
chr1:91268946 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3773-1091G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91268946 | |||||||
chr1:91269127 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3773-1272A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269127 | |||||||
chr1:91269215 | A | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3773-1360T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269215 | |||||||
chr1:91269230 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3773-1375G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269230 | |||||||
chr1:91269255 | T | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0101 |
3 | NA18939.hp1 NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3773-1400A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269255 | |||||||
chr1:91269269 | C | T | 2 | a0001c0001t0001g0282 a0001c0016t0001g0141 |
2 | HG00558.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3773-1414G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269269 | |||||||
chr1:91269348 | C | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.3773-1493G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269348 | |||||||
chr1:91269353 | T | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3773-1498A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269353 | |||||||
chr1:91269393 | TGAAA | T | 6 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0168 others(3): Show |
6 | HG02055.hp1 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.3773-1542_3773-153 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269393 | |||||||
chr1:91269438 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3773-1583A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269438 | |||||||
chr1:91269618 | G | A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3773-1763C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269618 | |||||||
chr1:91269631 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3773-1776C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269631 | |||||||
chr1:91269756 | G | A | 81 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(78): Show |
82 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.3773-1901C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269756 | |||||||
chr1:91269799 | A | G | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.3773-1944T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269799 | |||||||
chr1:91269877 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG02040.hp2 HG02074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3773-2022C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91269877 | |||||||
chr1:91270323 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3773-2468A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270323 | |||||||
chr1:91270351 | T | G | 5 | a0001c0002t0001g0029 a0001c0002t0001g0034 a0001c0002t0001g0036 others(2): Show |
5 | HG01952.hp2 NA18940.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.3773-2496A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270351 | |||||||
chr1:91270446 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(263): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.3773-2591A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270446 | |||||||
chr1:91270536 | G | A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3773-2681C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270536 | |||||||
chr1:91270574 | T | TA | 74 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0056 others(71): Show |
74 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.3773-2720dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270574 | |||||||
chr1:91270582 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3773-2727T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270582 | |||||||
chr1:91270582 | A | G | 20 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(17): Show |
20 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.3773-2727T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91270582 | |||||||
chr1:91271119 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3772+2593C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271119 | |||||||
chr1:91271177 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3772+2535G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271177 | |||||||
chr1:91271313 | C | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3772+2399G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271313 | |||||||
chr1:91271409 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3772+2303T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271409 | |||||||
chr1:91271574 | T | C | 1 | a0001c0002t0001g0039 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3772+2138A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271574 | |||||||
chr1:91271579 | A | G | 1 | a0001c0002t0001g0027 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3772+2133T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271579 | |||||||
chr1:91271650 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3772+2062C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271650 | |||||||
chr1:91271689 | A | G | 1 | a0001c0004t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3772+2023T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271689 | |||||||
chr1:91271707 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3772+2005T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271707 | |||||||
chr1:91271867 | C | A | 1 | a0001c0002t0001g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3772+1845G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271867 | |||||||
chr1:91271948 | A | C | 17 | a0002c0003t0001g0324 a0002c0003t0001g0325 a0002c0003t0001g0326 others(14): Show |
17 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3772+1764T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91271948 | |||||||
chr1:91272152 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3772+1560A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272152 | |||||||
chr1:91272158 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3772+1554T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272158 | |||||||
chr1:91272340 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3772+1372G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272340 | |||||||
chr1:91272360 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3772+1352A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272360 | |||||||
chr1:91272543 | A | AGACAAGC | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3772+1162_3772+116 others(11): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272543 | |||||||
chr1:91272641 | G | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0101 |
3 | NA18939.hp1 NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3772+1071C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272641 | |||||||
chr1:91272654 | A | C | 26 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(23): Show |
27 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.3772+1058T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272654 | |||||||
chr1:91272707 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3772+1005A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272707 | |||||||
chr1:91272708 | G | T | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3772+1004C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91272708 | |||||||
chr1:91273051 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3772+661G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273051 | |||||||
chr1:91273205 | T | C | 81 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(78): Show |
82 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.3772+507A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273205 | |||||||
chr1:91273327 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3772+385A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273327 | |||||||
chr1:91273555 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3772+157G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273555 | |||||||
chr1:91273603 | G | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3772+109C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273603 | |||||||
chr1:91273676 | A | G | 1 | a0004c0008t0001g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3772+36T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 34/38 | chr1 | 91273676 | |||||||
chr1:91273900 | A | C | 50 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(47): Show |
51 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.3669-85T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91273900 | |||||||
chr1:91274001 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3669-186A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274001 | |||||||
chr1:91274019 | A | G | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.3669-204T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274019 | |||||||
chr1:91274135 | G | T | 1 | a0001c0002t0001g0055 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3669-320C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274135 | |||||||
chr1:91274176 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3669-361A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274176 | |||||||
chr1:91274285 | T | C | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.3668+445A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274285 | |||||||
chr1:91274314 | T | C | 1 | a0001c0002t0005g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3668+416A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274314 | |||||||
chr1:91274367 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3668+363A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274367 | |||||||
chr1:91274369 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3668+361C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 33/38 | chr1 | 91274369 | |||||||
chr1:91274906 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3589-97G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91274906 | |||||||
chr1:91274985 | A | AT | 303 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(300): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.3589-177dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91274985 | |||||||
chr1:91274985 | A | ATT | 16 | a0001c0001t0001g0103 a0001c0001t0001g0261 a0001c0001t0001g0314 others(13): Show |
16 | HG01952.hp2 HG01978.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3589-178_3589-177d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91274985 | |||||||
chr1:91275205 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3589-396C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275205 | |||||||
chr1:91275246 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3589-437C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275246 | |||||||
chr1:91275263 | G | A | 1 | a0002c0003t0001g0344 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3589-454C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275263 | |||||||
chr1:91275415 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(263): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.3589-606C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275415 | |||||||
chr1:91275463 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3589-654T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275463 | |||||||
chr1:91275504 | A | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0081 others(5): Show |
8 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3589-695T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275504 | |||||||
chr1:91275585 | C | A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3589-776G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275585 | |||||||
chr1:91275758 | A | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3588+870T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91275758 | |||||||
chr1:91276054 | C | A | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3588+574G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91276054 | |||||||
chr1:91276142 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3588+486T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91276142 | |||||||
chr1:91276382 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3588+246C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91276382 | |||||||
chr1:91276498 | T | C | 78 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(75): Show |
79 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.3588+130A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91276498 | |||||||
chr1:91276537 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3588+91A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 32/38 | chr1 | 91276537 | |||||||
chr1:91276797 | A | G | 1 | a0001c0017t0001g0351 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3473-54T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 31/38 | chr1 | 91276797 | |||||||
chr1:91276862 | AATT | A | 40 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(37): Show |
41 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3472+117_3472+119d others(5): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 31/38 | chr1 | 91276862 | |||||||
chr1:91277208 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0314 |
2 | HG03130.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3392-146C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277208 | |||||||
chr1:91277231 | A | G | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-169T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277231 | |||||||
chr1:91277244 | A | C | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3392-182T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277244 | |||||||
chr1:91277373 | C | T | 1 | a0001c0004t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3392-311G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277373 | |||||||
chr1:91277391 | A | C | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-329T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277391 | |||||||
chr1:91277405 | A | G | 5 | a0001c0004t0001g0171 a0001c0004t0001g0172 a0001c0004t0001g0173 others(2): Show |
5 | HG01074.hp2 HG02738.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.3392-343T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277405 | |||||||
chr1:91277483 | G | A | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3392-421C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277483 | |||||||
chr1:91277500 | C | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-438G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277500 | |||||||
chr1:91277502 | G | GGTGTGT | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-441_3392-440i others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277502 | |||||||
chr1:91277504 | TGG | T | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-444_3392-443d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277504 | |||||||
chr1:91277506 | G | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-444C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277506 | |||||||
chr1:91277506 | GGT | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(288): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.3392-446_3392-445d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277506 | |||||||
chr1:91277534 | TTA | T | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-474_3392-473d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277534 | |||||||
chr1:91277539 | T | G | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3392-477A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277539 | |||||||
chr1:91277566 | GTATAATA others(13): Show |
G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(152): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.3392-524_3392-505d others(22): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277566 | |||||||
chr1:91277588 | A | ATATACTA others(5): Show |
201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.3392-527_3392-526i others(14): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277588 | |||||||
chr1:91277600 | C | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.3392-538G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277600 | |||||||
chr1:91277602 | T | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.3392-540A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277602 | |||||||
chr1:91277604 | A | ATAC | 201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.3392-543_3392-542i others(5): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277604 | |||||||
chr1:91277613 | C | A | 201 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(198): Show |
203 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.3392-551G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277613 | |||||||
chr1:91277637 | T | TAC | 183 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(180): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.3392-577_3392-576d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277637 | |||||||
chr1:91277665 | TAA | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-605_3392-604d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277665 | |||||||
chr1:91277674 | C | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-612G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277674 | |||||||
chr1:91277678 | A | T | 4 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-616T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277678 | |||||||
chr1:91277740 | TATATATA others(11): Show |
T | 8 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(5): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-696_3392-679d others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277740 | |||||||
chr1:91277766 | CTAATATA others(3): Show |
C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-714_3392-705d others(12): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277766 | |||||||
chr1:91277780 | G | GTATATAC others(30): Show |
1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3392-755_3392-719d others(39): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277780 | |||||||
chr1:91277781 | T | C | 12 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
12 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3392-719A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277781 | |||||||
chr1:91277852 | T | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-790A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277852 | |||||||
chr1:91277860 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3392-798T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277860 | |||||||
chr1:91277875 | T | C | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.3392-813A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277875 | |||||||
chr1:91277898 | C | CCTATATA others(31): Show |
1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3392-837_3392-836i others(40): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277898 | |||||||
chr1:91277899 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3392-837A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277899 | |||||||
chr1:91277899 | T | TTA | 85 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0206 others(82): Show |
86 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.3392-839_3392-838d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277899 | |||||||
chr1:91277899 | T | TTATATAT others(31): Show |
257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(254): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3392-838_3392-837i others(40): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277899 | |||||||
chr1:91277899 | T | TTATATAT others(67): Show |
1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-838_3392-837i others(76): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277899 | |||||||
chr1:91277906 | T | TATAATAT others(31): Show |
9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-845_3392-844i others(40): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277906 | |||||||
chr1:91277921 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3392-859A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277921 | |||||||
chr1:91277988 | T | A | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3392-926A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91277988 | |||||||
chr1:91278253 | T | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0075 |
2 | HG02080.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.3392-1191A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278253 | |||||||
chr1:91278291 | T | C | 81 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(78): Show |
82 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.3392-1229A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278291 | |||||||
chr1:91278411 | G | A | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 |
3 | HG02109.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3392-1349C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278411 | |||||||
chr1:91278484 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-1422C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278484 | |||||||
chr1:91278533 | A | G | 26 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(23): Show |
27 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.3392-1471T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278533 | |||||||
chr1:91278643 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3392-1581C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91278643 | |||||||
chr1:91279136 | T | C | 1 | a0001c0002t0001g0055 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3392-2074A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279136 | |||||||
chr1:91279151 | C | T | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-2089G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279151 | |||||||
chr1:91279277 | A | C | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3392-2215T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279277 | |||||||
chr1:91279277 | A | G | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3392-2215T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279277 | |||||||
chr1:91279327 | A | C | 1 | a0001c0007t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3392-2265T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279327 | |||||||
chr1:91279402 | C | G | 1 | a0001c0002t0005g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3392-2340G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279402 | |||||||
chr1:91279442 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3392-2380G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279442 | |||||||
chr1:91279479 | A | G | 40 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(37): Show |
41 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3392-2417T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279479 | |||||||
chr1:91279647 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3392-2585A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279647 | |||||||
chr1:91279678 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-2616T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279678 | |||||||
chr1:91279697 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3392-2635C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279697 | |||||||
chr1:91279739 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3392-2677C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279739 | |||||||
chr1:91279854 | C | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.3392-2792G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91279854 | |||||||
chr1:91280097 | T | C | 1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3392-3035A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280097 | |||||||
chr1:91280280 | T | C | 28 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(25): Show |
28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3392-3218A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280280 | |||||||
chr1:91280307 | G | C | 1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3392-3245C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280307 | |||||||
chr1:91280419 | G | A | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-3357C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280419 | |||||||
chr1:91280425 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3392-3363G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280425 | |||||||
chr1:91280642 | CCT | C | 9 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-3582_3392-358 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280642 | |||||||
chr1:91280740 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(277): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.3392-3678T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280740 | |||||||
chr1:91280765 | C | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3392-3703G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91280765 | |||||||
chr1:91281285 | A | G | 1 | a0002c0003t0001g0332 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3392-4223T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281285 | |||||||
chr1:91281361 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-4299A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281361 | |||||||
chr1:91281449 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.3392-4387G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281449 | |||||||
chr1:91281529 | C | T | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-4467G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281529 | |||||||
chr1:91281705 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3392-4643A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281705 | |||||||
chr1:91281724 | T | C | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-4662A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281724 | |||||||
chr1:91281757 | C | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-4695G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281757 | |||||||
chr1:91281851 | C | G | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3392-4789G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91281851 | |||||||
chr1:91282090 | A | G | 28 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(25): Show |
28 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.3392-5028T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282090 | |||||||
chr1:91282293 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3392-5231T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282293 | |||||||
chr1:91282349 | A | G | 2 | a0001c0004t0001g0164 a0001c0004t0001g0167 |
2 | HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3392-5287T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282349 | |||||||
chr1:91282625 | C | CA | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-5564dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282625 | |||||||
chr1:91282860 | A | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3392-5798T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282860 | |||||||
chr1:91282982 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3392-5920T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91282982 | |||||||
chr1:91283213 | T | C | 1 | a0004c0008t0001g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3392-6151A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91283213 | |||||||
chr1:91283407 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3392-6345G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91283407 | |||||||
chr1:91283456 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-6394A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91283456 | |||||||
chr1:91283986 | C | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-6924G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91283986 | |||||||
chr1:91284087 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-7025C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284087 | |||||||
chr1:91284250 | A | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3392-7188T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284250 | |||||||
chr1:91284250 | AT | A | 10 | a0001c0001t0002g0092 a0001c0005t0002g0144 a0001c0005t0002g0145 others(7): Show |
10 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.3392-7189delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284250 | |||||||
chr1:91284296 | T | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(24): Show |
28 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.3392-7234A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284296 | |||||||
chr1:91284361 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-7299G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284361 | |||||||
chr1:91284839 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(276): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.3392-7777A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284839 | |||||||
chr1:91284867 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-7805G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284867 | |||||||
chr1:91284971 | G | A | 1 | a0001c0002t0001g0024 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3392-7909C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91284971 | |||||||
chr1:91285069 | C | T | 14 | a0002c0003t0001g0324 a0002c0003t0001g0325 a0002c0003t0001g0326 others(11): Show |
14 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3392-8007G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285069 | |||||||
chr1:91285123 | A | G | 29 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0186 others(26): Show |
30 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-8061T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285123 | |||||||
chr1:91285332 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3392-8270G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285332 | |||||||
chr1:91285366 | T | C | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3392-8304A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285366 | |||||||
chr1:91285608 | A | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-8546T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285608 | |||||||
chr1:91285618 | T | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0220 |
2 | NA18954.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3392-8556A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285618 | |||||||
chr1:91285624 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3392-8562A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285624 | |||||||
chr1:91285905 | C | T | 10 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(7): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3392-8843G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285905 | |||||||
chr1:91285979 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3392-8917G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91285979 | |||||||
chr1:91286125 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3392-9063A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286125 | |||||||
chr1:91286229 | T | A | 1 | a0001c0001t0001g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3392-9167A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286229 | |||||||
chr1:91286249 | G | A | 21 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0260 others(18): Show |
21 | HG00408.hp1 HG01928.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.3392-9187C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286249 | |||||||
chr1:91286419 | A | G | 2 | a0001c0001t0001g0201 a0003c0009t0001g0345 |
2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3392-9357T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286419 | |||||||
chr1:91286650 | G | A | 5 | a0001c0004t0001g0161 a0001c0004t0001g0162 a0001c0004t0001g0168 others(2): Show |
5 | HG02055.hp1 HG03139.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3392-9588C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286650 | |||||||
chr1:91286666 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-9604G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286666 | |||||||
chr1:91286685 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3392-9623A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286685 | |||||||
chr1:91286812 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3392-9750C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286812 | |||||||
chr1:91286827 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3392-9765C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286827 | |||||||
chr1:91286828 | C | T | 6 | a0001c0007t0001g0188 a0001c0007t0001g0190 a0001c0007t0001g0193 others(3): Show |
6 | HG00609.hp1 NA18943.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.3392-9766G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286828 | |||||||
chr1:91286907 | C | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-9845G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286907 | |||||||
chr1:91286918 | G | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3392-9856C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286918 | |||||||
chr1:91286942 | G | A | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3392-9880C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286942 | |||||||
chr1:91286950 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3392-9888C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286950 | |||||||
chr1:91286965 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3392-9903G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286965 | |||||||
chr1:91286998 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0101 |
3 | NA18939.hp1 NA18959.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3392-9936A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91286998 | |||||||
chr1:91287017 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3392-9955G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287017 | |||||||
chr1:91287018 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3392-9956C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287018 | |||||||
chr1:91287025 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0108 a0001c0001t0001g0117 others(1): Show |
4 | HG01255.hp1 HG01516.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-9963G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287025 | |||||||
chr1:91287031 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-9969A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287031 | |||||||
chr1:91287066 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3392-10004G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287066 | |||||||
chr1:91287089 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3392-10027A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287089 | |||||||
chr1:91287089 | T | G | 1 | a0001c0001t0001g0350 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3392-10027A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287089 | |||||||
chr1:91287094 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3392-10032C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287094 | |||||||
chr1:91287098 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3392-10036G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287098 | |||||||
chr1:91287107 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.3392-10045T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287107 | |||||||
chr1:91287130 | C | T | 1 | a0001c0002t0001g0039 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3392-10068G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287130 | |||||||
chr1:91287226 | A | G | 1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3392-10164T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287226 | |||||||
chr1:91287311 | T | A | 1 | a0001c0002t0001g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3392-10249A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287311 | |||||||
chr1:91287311 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3392-10249A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287311 | |||||||
chr1:91287312 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3392-10250G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287312 | |||||||
chr1:91287319 | G | C | 5 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0306 others(2): Show |
5 | HG01891.hp2 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3392-10257C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287319 | |||||||
chr1:91287324 | A | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-10262T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287324 | |||||||
chr1:91287342 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3392-10280T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287342 | |||||||
chr1:91287362 | C | T | 1 | a0001c0007t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3392-10300G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287362 | |||||||
chr1:91287363 | A | C | 7 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG02258.hp2 NA18946.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3392-10301T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287363 | |||||||
chr1:91287363 | A | G | 1 | a0001c0007t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3392-10301T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287363 | |||||||
chr1:91287384 | C | A | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.3392-10322G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287384 | |||||||
chr1:91287389 | T | C | 2 | a0001c0001t0001g0272 a0001c0007t0001g0190 |
2 | HG00544.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3392-10327A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287389 | |||||||
chr1:91287391 | G | A | 1 | a0001c0007t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3392-10329C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287391 | |||||||
chr1:91287400 | G | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(174): Show |
179 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.3392-10338C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287400 | |||||||
chr1:91287403 | T | G | 173 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(170): Show |
175 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.3392-10341A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287403 | |||||||
chr1:91287416 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(125): Show |
129 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.3392-10354C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287416 | |||||||
chr1:91287416 | G | T | 1 | a0001c0007t0001g0190 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3392-10354C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287416 | |||||||
chr1:91287417 | T | G | 134 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
135 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.3392-10355A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287417 | |||||||
chr1:91287419 | C | A | 134 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
135 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.3392-10357G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287419 | |||||||
chr1:91287425 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3392-10363G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287425 | |||||||
chr1:91287501 | A | G | 150 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
151 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.3392-10439T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287501 | |||||||
chr1:91287527 | G | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
154 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.3392-10465C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287527 | |||||||
chr1:91287596 | A | G | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3392-10534T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287596 | |||||||
chr1:91287597 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3392-10535C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287597 | |||||||
chr1:91287604 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3392-10542T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287604 | |||||||
chr1:91287610 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3392-10548G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287610 | |||||||
chr1:91287611 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3392-10549G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287611 | |||||||
chr1:91287626 | G | A | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-10564C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287626 | |||||||
chr1:91287638 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3392-10576G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287638 | |||||||
chr1:91287653 | G | C | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-10591C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287653 | |||||||
chr1:91287700 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3392-10638G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287700 | |||||||
chr1:91287714 | C | T | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3392-10652G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287714 | |||||||
chr1:91287721 | C | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-10659G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287721 | |||||||
chr1:91287722 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-10660C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287722 | |||||||
chr1:91287886 | T | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-10824A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91287886 | |||||||
chr1:91288035 | G | A | 1 | a0001c0017t0001g0351 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3392-10973C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288035 | |||||||
chr1:91288156 | C | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
180 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.3392-11094G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288156 | |||||||
chr1:91288163 | C | T | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
180 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.3392-11101G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288163 | |||||||
chr1:91288170 | G | A | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
180 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.3392-11108C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288170 | |||||||
chr1:91288330 | C | T | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3392-11268G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288330 | |||||||
chr1:91288349 | G | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-11287C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288349 | |||||||
chr1:91288366 | CT | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.3392-11305delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288366 | |||||||
chr1:91288366 | CTT | C | 34 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0097 others(31): Show |
35 | HG00280.hp1 HG00639.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.3392-11306_3392-11 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288366 | |||||||
chr1:91288383 | T | A | 324 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(321): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.3392-11321A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288383 | |||||||
chr1:91288384 | T | A | 326 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(323): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.3392-11322A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288384 | |||||||
chr1:91288443 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
154 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.3392-11381C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288443 | |||||||
chr1:91288483 | T | A | 222 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(219): Show |
224 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.3392-11421A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288483 | |||||||
chr1:91288576 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-11514A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288576 | |||||||
chr1:91288579 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3392-11517G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288579 | |||||||
chr1:91288590 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-11528A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288590 | |||||||
chr1:91288696 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3392-11634T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288696 | |||||||
chr1:91288794 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3392-11732T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288794 | |||||||
chr1:91288858 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0076 others(6): Show |
10 | HG00280.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.3392-11796C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288858 | |||||||
chr1:91288904 | C | CG | 9 | a0001c0001t0001g0014 a0001c0001t0001g0111 a0001c0001t0001g0131 others(6): Show |
9 | HG02602.hp2 HG02723.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-11843dupC | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288904 | |||||||
chr1:91288928 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3392-11866G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288928 | |||||||
chr1:91288945 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3392-11883C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288945 | |||||||
chr1:91288981 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3392-11919G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288981 | |||||||
chr1:91288996 | G | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-11934C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91288996 | |||||||
chr1:91289036 | C | T | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-11974G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289036 | |||||||
chr1:91289058 | T | A | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3392-11996A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289058 | |||||||
chr1:91289063 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-12001C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289063 | |||||||
chr1:91289144 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-12082T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289144 | |||||||
chr1:91289164 | C | T | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-12102G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289164 | |||||||
chr1:91289169 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3392-12107G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289169 | |||||||
chr1:91289182 | C | T | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3392-12120G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289182 | |||||||
chr1:91289193 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3392-12131G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289193 | |||||||
chr1:91289206 | C | T | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3392-12144G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289206 | |||||||
chr1:91289215 | T | C | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-12153A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289215 | |||||||
chr1:91289222 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3392-12160G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289222 | |||||||
chr1:91289230 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.3392-12168G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289230 | |||||||
chr1:91289281 | C | T | 9 | a0001c0002t0001g0032 a0001c0005t0002g0144 a0001c0005t0002g0145 others(6): Show |
9 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.3392-12219G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289281 | |||||||
chr1:91289299 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-12237G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289299 | |||||||
chr1:91289346 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3392-12284G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289346 | |||||||
chr1:91289361 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3392-12299C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289361 | |||||||
chr1:91289416 | G | A | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3392-12354C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289416 | |||||||
chr1:91289420 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-12358C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289420 | |||||||
chr1:91289510 | C | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.3392-12448G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289510 | |||||||
chr1:91289546 | C | T | 6 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(3): Show |
6 | NA18944.hp2 NA18965.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.3392-12484G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289546 | |||||||
chr1:91289576 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3392-12514T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289576 | |||||||
chr1:91289730 | G | A | 1 | a0001c0004t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3392-12668C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289730 | |||||||
chr1:91289755 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3392-12693G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289755 | |||||||
chr1:91289805 | C | T | 2 | a0001c0001t0001g0140 a0001c0004t0001g0161 |
2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3392-12743G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289805 | |||||||
chr1:91289829 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3392-12767G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289829 | |||||||
chr1:91289852 | A | AAGAGGGA others(16): Show |
1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3392-12813_3392-12 others(29): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289852 | |||||||
chr1:91289978 | C | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-12916G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91289978 | |||||||
chr1:91290083 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0022 |
2 | NA18991.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.3392-13021G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290083 | |||||||
chr1:91290113 | C | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.3392-13051G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290113 | |||||||
chr1:91290142 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3392-13080G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290142 | |||||||
chr1:91290218 | C | A | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-13156G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290218 | |||||||
chr1:91290227 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-13165T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290227 | |||||||
chr1:91290320 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.3392-13258C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290320 | |||||||
chr1:91290727 | C | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-13665G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290727 | |||||||
chr1:91290859 | C | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | NA18946.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.3392-13797G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290859 | |||||||
chr1:91290945 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.3392-13883T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290945 | |||||||
chr1:91290964 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-13902G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290964 | |||||||
chr1:91290964 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3392-13902G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290964 | |||||||
chr1:91290969 | T | C | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.3392-13907A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91290969 | |||||||
chr1:91291004 | G | A | 2 | a0001c0002t0001g0024 a0002c0003t0001g0339 |
2 | HG02055.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3392-13942C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291004 | |||||||
chr1:91291063 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3392-14001C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291063 | |||||||
chr1:91291177 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3392-14115G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291177 | |||||||
chr1:91291224 | A | T | 1 | a0001c0001t0001g0357 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3392-14162T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291224 | |||||||
chr1:91291257 | T | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-14195A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291257 | |||||||
chr1:91291314 | T | C | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3392-14252A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291314 | |||||||
chr1:91291330 | G | C | 1 | a0001c0004t0001g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3392-14268C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291330 | |||||||
chr1:91291429 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3392-14367G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291429 | |||||||
chr1:91291450 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3392-14388C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291450 | |||||||
chr1:91291548 | T | G | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3392-14486A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291548 | |||||||
chr1:91291573 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG01109.hp1 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3392-14511C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291573 | |||||||
chr1:91291616 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3392-14554G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291616 | |||||||
chr1:91291730 | A | C | 49 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(46): Show |
50 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.3392-14668T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291730 | |||||||
chr1:91291732 | G | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3392-14670C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291732 | |||||||
chr1:91291747 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3392-14685G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291747 | |||||||
chr1:91291820 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3392-14758G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91291820 | |||||||
chr1:91292046 | G | A | 1 | a0006c0010t0001g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3392-14984C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292046 | |||||||
chr1:91292050 | C | T | 1 | a0001c0001t0001g0356 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3392-14988G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292050 | |||||||
chr1:91292087 | C | G | 1 | a0001c0001t0001g0074 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3392-15025G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292087 | |||||||
chr1:91292091 | A | T | 1 | a0001c0001t0001g0074 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3392-15029T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292091 | |||||||
chr1:91292307 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3392-15245A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292307 | |||||||
chr1:91292308 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3392-15246C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292308 | |||||||
chr1:91292332 | T | C | 354 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(351): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.3392-15270A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292332 | |||||||
chr1:91292418 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-15356T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292418 | |||||||
chr1:91292443 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3392-15381G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292443 | |||||||
chr1:91292551 | G | C | 1 | a0001c0001t0001g0302 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3392-15489C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292551 | |||||||
chr1:91292669 | C | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 |
3 | HG01257.hp1 HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.3392-15607G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292669 | |||||||
chr1:91292671 | A | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3392-15609T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292671 | |||||||
chr1:91292692 | G | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-15630C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292692 | |||||||
chr1:91292714 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3392-15652A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292714 | |||||||
chr1:91292736 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3392-15674A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292736 | |||||||
chr1:91292786 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-15724A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292786 | |||||||
chr1:91292803 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3392-15741A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292803 | |||||||
chr1:91292935 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3392-15873T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91292935 | |||||||
chr1:91293059 | G | T | 3 | a0005c0006t0001g0189 a0005c0006t0001g0191 a0005c0006t0001g0192 |
3 | NA18943.hp2 NA18981.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3392-15997C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293059 | |||||||
chr1:91293134 | T | C | 1 | a0001c0004t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3392-16072A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293134 | |||||||
chr1:91293159 | T | C | 4 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(1): Show |
4 | HG02135.hp2 HG02523.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-16097A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293159 | |||||||
chr1:91293164 | C | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
11 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.3392-16102G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293164 | |||||||
chr1:91293172 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3392-16110C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293172 | |||||||
chr1:91293291 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3392-16229C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293291 | |||||||
chr1:91293396 | A | G | 3 | a0001c0001t0001g0194 a0006c0010t0001g0243 a0006c0010t0001g0244 |
3 | HG02630.hp2 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3392-16334T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293396 | |||||||
chr1:91293433 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(151): Show |
155 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.3392-16371T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293433 | |||||||
chr1:91293591 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3392-16529C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293591 | |||||||
chr1:91293633 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3392-16571G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293633 | |||||||
chr1:91293642 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-16580C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293642 | |||||||
chr1:91293809 | A | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-16747T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293809 | |||||||
chr1:91293866 | G | A | 1 | a0002c0003t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3392-16804C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293866 | |||||||
chr1:91293870 | T | C | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-16808A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293870 | |||||||
chr1:91293943 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3392-16881C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293943 | |||||||
chr1:91293965 | C | T | 2 | a0001c0002t0001g0024 a0002c0003t0001g0336 |
2 | HG03491.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.3392-16903G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91293965 | |||||||
chr1:91294014 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3392-16952T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294014 | |||||||
chr1:91294022 | G | T | 2 | a0002c0003t0001g0332 a0002c0003t0001g0333 |
2 | HG02258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3392-16960C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294022 | |||||||
chr1:91294105 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3392-17043G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294105 | |||||||
chr1:91294144 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3392-17082T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294144 | |||||||
chr1:91294281 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.3392-17219C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294281 | |||||||
chr1:91294307 | G | C | 7 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3392-17245C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294307 | |||||||
chr1:91294362 | A | G | 78 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(75): Show |
80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.3392-17300T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294362 | |||||||
chr1:91294375 | C | G | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3392-17313G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294375 | |||||||
chr1:91294819 | A | T | 78 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(75): Show |
80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.3392-17757T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294819 | |||||||
chr1:91294955 | C | T | 1 | a0001c0002t0001g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3392-17893G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91294955 | |||||||
chr1:91295015 | T | A | 174 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(171): Show |
175 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.3392-17953A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295015 | |||||||
chr1:91295307 | T | G | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.3391+18042A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295307 | |||||||
chr1:91295410 | T | C | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3391+17939A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295410 | |||||||
chr1:91295580 | G | C | 1 | a0001c0001t0001g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3391+17769C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295580 | |||||||
chr1:91295956 | A | G | 1 | a0001c0004t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3391+17393T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295956 | |||||||
chr1:91295990 | G | T | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3391+17359C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91295990 | |||||||
chr1:91296047 | T | C | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+17302A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296047 | |||||||
chr1:91296134 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+17215A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296134 | |||||||
chr1:91296160 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3391+17189G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296160 | |||||||
chr1:91296196 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+17153C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296196 | |||||||
chr1:91296211 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3391+17138C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296211 | |||||||
chr1:91296223 | A | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(77): Show |
81 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.3391+17126T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296223 | |||||||
chr1:91296300 | C | T | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.3391+17049G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296300 | |||||||
chr1:91296393 | G | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3391+16956C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296393 | |||||||
chr1:91296543 | G | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3391+16806C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296543 | |||||||
chr1:91296578 | A | C | 1 | a0001c0002t0001g0008 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3391+16771T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296578 | |||||||
chr1:91296660 | G | A | 1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3391+16689C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296660 | |||||||
chr1:91296760 | T | G | 2 | a0002c0003t0001g0337 a0002c0003t0001g0342 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3391+16589A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296760 | |||||||
chr1:91296838 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+16511C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296838 | |||||||
chr1:91296860 | G | A | 3 | a0001c0005t0002g0147 a0001c0005t0002g0148 a0001c0005t0002g0150 |
3 | HG02083.hp2 NA18953.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.3391+16489C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296860 | |||||||
chr1:91296866 | G | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+16483C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296866 | |||||||
chr1:91296878 | A | G | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3391+16471T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296878 | |||||||
chr1:91296888 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3391+16461A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296888 | |||||||
chr1:91296989 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3391+16360C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91296989 | |||||||
chr1:91297026 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3391+16323C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297026 | |||||||
chr1:91297077 | C | T | 1 | a0001c0004t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3391+16272G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297077 | |||||||
chr1:91297078 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3391+16271C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297078 | |||||||
chr1:91297151 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0234 others(2): Show |
6 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3391+16198C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297151 | |||||||
chr1:91297206 | T | A | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3391+16143A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297206 | |||||||
chr1:91297233 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3391+16116C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297233 | |||||||
chr1:91297239 | G | A | 1 | a0001c0017t0001g0351 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3391+16110C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297239 | |||||||
chr1:91297290 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+16059G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297290 | |||||||
chr1:91297329 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+16020C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297329 | |||||||
chr1:91297362 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3391+15987G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297362 | |||||||
chr1:91297593 | C | G | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+15756G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297593 | |||||||
chr1:91297781 | C | T | 355 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(352): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.3391+15568G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297781 | |||||||
chr1:91297782 | C | T | 1 | a0001c0007t0001g0193 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3391+15567G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297782 | |||||||
chr1:91297882 | G | A | 18 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0324 others(15): Show |
19 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.3391+15467C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297882 | |||||||
chr1:91297904 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3391+15445C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297904 | |||||||
chr1:91297923 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3391+15426C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297923 | |||||||
chr1:91297937 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+15412G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297937 | |||||||
chr1:91297944 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3391+15405A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297944 | |||||||
chr1:91297953 | T | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3391+15396A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297953 | |||||||
chr1:91297957 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+15392A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91297957 | |||||||
chr1:91298021 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3391+15328T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298021 | |||||||
chr1:91298137 | G | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.3391+15212C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298137 | |||||||
chr1:91298163 | C | T | 1 | a0002c0003t0001g0325 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3391+15186G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298163 | |||||||
chr1:91298224 | G | A | 1 | a0001c0002t0001g0008 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3391+15125C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298224 | |||||||
chr1:91298300 | G | A | 34 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0200 others(31): Show |
34 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.3391+15049C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298300 | |||||||
chr1:91298301 | T | A | 34 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0200 others(31): Show |
34 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.3391+15048A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298301 | |||||||
chr1:91298310 | G | C | 34 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0200 others(31): Show |
34 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.3391+15039C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298310 | |||||||
chr1:91298312 | T | C | 34 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0200 others(31): Show |
34 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.3391+15037A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298312 | |||||||
chr1:91298359 | G | T | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3391+14990C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298359 | |||||||
chr1:91298435 | A | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3391+14914T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298435 | |||||||
chr1:91298442 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+14907G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298442 | |||||||
chr1:91298511 | G | GA | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3391+14837dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298511 | |||||||
chr1:91298553 | C | A | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3391+14796G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298553 | |||||||
chr1:91298569 | T | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3391+14780A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298569 | |||||||
chr1:91298756 | C | G | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG02040.hp2 HG02074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+14593G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298756 | |||||||
chr1:91298764 | G | T | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3391+14585C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298764 | |||||||
chr1:91298837 | C | A | 1 | a0001c0002t0001g0139 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3391+14512G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298837 | |||||||
chr1:91298856 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+14493C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298856 | |||||||
chr1:91298894 | A | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+14455T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298894 | |||||||
chr1:91298931 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3391+14418G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91298931 | |||||||
chr1:91299034 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3391+14315G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299034 | |||||||
chr1:91299050 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+14299G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299050 | |||||||
chr1:91299131 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3391+14218A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299131 | |||||||
chr1:91299149 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3391+14200T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299149 | |||||||
chr1:91299162 | T | C | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+14187A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299162 | |||||||
chr1:91299308 | G | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3391+14041C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299308 | |||||||
chr1:91299355 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3391+13994C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299355 | |||||||
chr1:91299407 | C | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3391+13942G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299407 | |||||||
chr1:91299430 | G | A | 57 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(54): Show |
58 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.3391+13919C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299430 | |||||||
chr1:91299582 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0234 others(2): Show |
6 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3391+13767C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299582 | |||||||
chr1:91299621 | T | A | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3391+13728A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299621 | |||||||
chr1:91299641 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+13708G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299641 | |||||||
chr1:91299666 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3391+13683A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299666 | |||||||
chr1:91299681 | A | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+13668T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299681 | |||||||
chr1:91299735 | A | G | 8 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0327 others(5): Show |
9 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3391+13614T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299735 | |||||||
chr1:91299750 | C | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.3391+13599G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299750 | |||||||
chr1:91299968 | A | T | 19 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.3391+13381T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91299968 | |||||||
chr1:91300014 | T | C | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+13335A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300014 | |||||||
chr1:91300109 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3391+13240G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300109 | |||||||
chr1:91300111 | G | A | 67 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(64): Show |
68 | HG00323.hp2 HG00735.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.3391+13238C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300111 | |||||||
chr1:91300186 | G | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3391+13163C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300186 | |||||||
chr1:91300259 | C | A | 1 | a0001c0001t0001g0300 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3391+13090G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300259 | |||||||
chr1:91300291 | A | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3391+13058T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300291 | |||||||
chr1:91300425 | C | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+12924G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300425 | |||||||
chr1:91300517 | C | T | 2 | a0001c0002t0001g0037 a0001c0002t0001g0041 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3391+12832G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300517 | |||||||
chr1:91300580 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+12769A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300580 | |||||||
chr1:91300615 | C | A | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3391+12734G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300615 | |||||||
chr1:91300656 | G | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+12693C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300656 | |||||||
chr1:91300661 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3391+12688A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300661 | |||||||
chr1:91300698 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3391+12651T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300698 | |||||||
chr1:91300736 | C | A | 221 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(218): Show |
223 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.3391+12613G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300736 | |||||||
chr1:91300766 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3391+12583A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300766 | |||||||
chr1:91300824 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3391+12525A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300824 | |||||||
chr1:91300839 | A | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+12510T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300839 | |||||||
chr1:91300894 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3391+12455A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91300894 | |||||||
chr1:91301014 | A | ATGAT | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+12331_3391+12 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301014 | |||||||
chr1:91301036 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0234 others(2): Show |
6 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.3391+12313G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301036 | |||||||
chr1:91301042 | T | C | 1 | a0001c0004t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3391+12307A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301042 | |||||||
chr1:91301069 | T | G | 77 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(74): Show |
79 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3391+12280A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301069 | |||||||
chr1:91301284 | A | G | 11 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.3391+12065T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301284 | |||||||
chr1:91301285 | G | C | 11 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.3391+12064C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301285 | |||||||
chr1:91301339 | A | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+12010T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301339 | |||||||
chr1:91301339 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | HG00639.hp1 HG01361.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+12010T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301339 | |||||||
chr1:91301340 | T | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0356 a0001c0001t0001g0357 others(1): Show |
4 | HG00639.hp1 HG01361.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+12009A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301340 | |||||||
chr1:91301400 | A | C | 2 | a0001c0007t0001g0188 a0001c0007t0001g0190 |
2 | HG00609.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3391+11949T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301400 | |||||||
chr1:91301410 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3391+11939G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301410 | |||||||
chr1:91301420 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(125): Show |
129 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.3391+11929A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301420 | |||||||
chr1:91301466 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3391+11883C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301466 | |||||||
chr1:91301484 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3391+11865A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301484 | |||||||
chr1:91301581 | C | G | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+11768G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301581 | |||||||
chr1:91301596 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3391+11753T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301596 | |||||||
chr1:91301642 | C | T | 355 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(352): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.3391+11707G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301642 | |||||||
chr1:91301686 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3391+11663C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301686 | |||||||
chr1:91301869 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3391+11480G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301869 | |||||||
chr1:91301903 | G | C | 348 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(345): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.3391+11446C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91301903 | |||||||
chr1:91302208 | A | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3391+11141T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302208 | |||||||
chr1:91302325 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02559.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+11024C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302325 | |||||||
chr1:91302367 | C | G | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3391+10982G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302367 | |||||||
chr1:91302417 | A | C | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3391+10932T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302417 | |||||||
chr1:91302435 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3391+10914T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302435 | |||||||
chr1:91302435 | A | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3391+10914T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302435 | |||||||
chr1:91302650 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3391+10699C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302650 | |||||||
chr1:91302713 | C | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3391+10636G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302713 | |||||||
chr1:91302740 | C | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+10609G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302740 | |||||||
chr1:91302742 | T | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+10607A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302742 | |||||||
chr1:91302762 | T | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3391+10587A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302762 | |||||||
chr1:91302763 | C | T | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(320): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.3391+10586G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302763 | |||||||
chr1:91302787 | T | TG | 20 | a0001c0001t0001g0062 a0001c0001t0001g0078 a0001c0001t0001g0091 others(17): Show |
20 | HG00741.hp2 HG01109.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.3391+10561dupC | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302787 | |||||||
chr1:91302895 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+10454C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302895 | |||||||
chr1:91302899 | G | A | 4 | a0001c0016t0001g0141 a0003c0013t0001g0143 a0004c0008t0001g0318 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+10450C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302899 | |||||||
chr1:91302984 | G | C | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3391+10365C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91302984 | |||||||
chr1:91303077 | A | G | 1 | a0001c0002t0005g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3391+10272T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303077 | |||||||
chr1:91303124 | T | A | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3391+10225A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303124 | |||||||
chr1:91303170 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.3391+10179T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303170 | |||||||
chr1:91303173 | C | G | 12 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(9): Show |
12 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.3391+10176G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303173 | |||||||
chr1:91303313 | T | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3391+10036A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303313 | |||||||
chr1:91303478 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+9871A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303478 | |||||||
chr1:91303538 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3391+9811A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303538 | |||||||
chr1:91303669 | CAT | C | 19 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.3391+9678_3391+967 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91303669 | |||||||
chr1:91304072 | C | T | 1 | a0002c0003t0001g0344 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3391+9277G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304072 | |||||||
chr1:91304150 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+9199G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304150 | |||||||
chr1:91304447 | AAG | A | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3391+8900_3391+890 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304447 | |||||||
chr1:91304497 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0107 |
2 | NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3391+8852C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304497 | |||||||
chr1:91304607 | C | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+8742G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304607 | |||||||
chr1:91304613 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.3391+8736G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304613 | |||||||
chr1:91304628 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+8721C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304628 | |||||||
chr1:91304633 | AT | A | 21 | a0001c0001t0001g0063 a0001c0001t0001g0153 a0001c0001t0001g0154 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.3391+8715delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304633 | |||||||
chr1:91304633 | ATT | A | 274 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(271): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.3391+8714_3391+871 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304633 | |||||||
chr1:91304697 | T | G | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3391+8652A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304697 | |||||||
chr1:91304832 | T | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3391+8517A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91304832 | |||||||
chr1:91305047 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+8302G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305047 | |||||||
chr1:91305167 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3391+8182G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305167 | |||||||
chr1:91305233 | T | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3391+8116A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305233 | |||||||
chr1:91305403 | T | G | 2 | a0005c0006t0001g0191 a0005c0006t0001g0192 |
2 | NA18981.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.3391+7946A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305403 | |||||||
chr1:91305496 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+7853C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305496 | |||||||
chr1:91305501 | TAG | T | 6 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0103 others(3): Show |
6 | NA18946.hp1 NA18981.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.3391+7846_3391+784 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305501 | |||||||
chr1:91305606 | T | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+7743A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91305606 | |||||||
chr1:91306060 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3391+7289G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306060 | |||||||
chr1:91306125 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3391+7224C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306125 | |||||||
chr1:91306281 | G | A | 1 | a0002c0003t0001g0344 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3391+7068C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306281 | |||||||
chr1:91306454 | C | A | 1 | a0001c0002t0001g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3391+6895G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306454 | |||||||
chr1:91306531 | T | C | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3391+6818A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306531 | |||||||
chr1:91306734 | A | G | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3391+6615T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306734 | |||||||
chr1:91306840 | C | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(123): Show |
127 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.3391+6509G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306840 | |||||||
chr1:91306845 | A | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.3391+6504T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306845 | |||||||
chr1:91306850 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3391+6499G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306850 | |||||||
chr1:91306893 | C | A | 7 | a0001c0001t0001g0185 a0001c0001t0001g0259 a0001c0001t0001g0270 others(4): Show |
7 | HG00544.hp2 NA18941.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+6456G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91306893 | |||||||
chr1:91307122 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3391+6227A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91307122 | |||||||
chr1:91307235 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(273): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.3391+6114A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91307235 | |||||||
chr1:91307489 | G | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+5860C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91307489 | |||||||
chr1:91307579 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3391+5770T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91307579 | |||||||
chr1:91307739 | C | A | 78 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(75): Show |
80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.3391+5610G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91307739 | |||||||
chr1:91308067 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+5282C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308067 | |||||||
chr1:91308246 | T | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3391+5103A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308246 | |||||||
chr1:91308342 | A | G | 128 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(125): Show |
129 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.3391+5007T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308342 | |||||||
chr1:91308378 | C | A | 1 | a0002c0003t0001g0348 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3391+4971G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308378 | |||||||
chr1:91308629 | C | G | 1 | a0001c0005t0002g0148 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3391+4720G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308629 | |||||||
chr1:91308874 | C | A | 1 | a0001c0004t0001g0175 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3391+4475G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308874 | |||||||
chr1:91308980 | A | G | 11 | a0001c0002t0001g0018 a0001c0002t0001g0033 a0001c0002t0001g0037 others(8): Show |
11 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.3391+4369T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91308980 | |||||||
chr1:91309068 | T | C | 3 | a0001c0004t0001g0164 a0001c0004t0001g0165 a0001c0004t0001g0167 |
3 | HG02965.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3391+4281A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309068 | |||||||
chr1:91309161 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3391+4188A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309161 | |||||||
chr1:91309183 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3391+4166T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309183 | |||||||
chr1:91309191 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3391+4158A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309191 | |||||||
chr1:91309263 | C | G | 80 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(77): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3391+4086G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309263 | |||||||
chr1:91309282 | A | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3391+4067T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309282 | |||||||
chr1:91309301 | G | T | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3391+4048C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309301 | |||||||
chr1:91309322 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3391+4027T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309322 | |||||||
chr1:91309440 | T | C | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3391+3909A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309440 | |||||||
chr1:91309828 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3391+3521A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309828 | |||||||
chr1:91309885 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3391+3464G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309885 | |||||||
chr1:91309930 | A | G | 5 | a0001c0001t0001g0257 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG01433.hp2 HG02300.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3391+3419T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309930 | |||||||
chr1:91309990 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3391+3359A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91309990 | |||||||
chr1:91310083 | T | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+3266A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310083 | |||||||
chr1:91310309 | T | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0122 others(1): Show |
4 | NA18970.hp1 NA19007.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+3040A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310309 | |||||||
chr1:91310387 | T | G | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3391+2962A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310387 | |||||||
chr1:91310446 | C | T | 1 | a0005c0006t0001g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3391+2903G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310446 | |||||||
chr1:91310569 | C | A | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3391+2780G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310569 | |||||||
chr1:91310613 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3391+2736C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310613 | |||||||
chr1:91310633 | G | C | 2 | a0001c0002t0001g0037 a0001c0002t0001g0041 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.3391+2716C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310633 | |||||||
chr1:91310704 | A | G | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+2645T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310704 | |||||||
chr1:91310723 | G | A | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.3391+2626C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310723 | |||||||
chr1:91310761 | G | A | 2 | a0002c0003t0001g0337 a0002c0003t0001g0342 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3391+2588C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310761 | |||||||
chr1:91310763 | C | T | 178 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(175): Show |
179 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.3391+2586G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91310763 | |||||||
chr1:91311024 | C | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+2325G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311024 | |||||||
chr1:91311149 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+2200A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311149 | |||||||
chr1:91311205 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3391+2144A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311205 | |||||||
chr1:91311472 | A | G | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.3391+1877T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311472 | |||||||
chr1:91311546 | A | G | 10 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(7): Show |
10 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.3391+1803T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311546 | |||||||
chr1:91311625 | C | CA | 91 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(88): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.3391+1723dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311625 | |||||||
chr1:91311791 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3391+1558G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311791 | |||||||
chr1:91311976 | G | A | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3391+1373C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91311976 | |||||||
chr1:91312041 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3391+1308G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312041 | |||||||
chr1:91312224 | G | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3391+1125C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312224 | |||||||
chr1:91312276 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0081 others(5): Show |
8 | HG01074.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.3391+1073A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312276 | |||||||
chr1:91312366 | G | A | 77 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(74): Show |
79 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.3391+983C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312366 | |||||||
chr1:91312518 | G | C | 1 | a0001c0005t0002g0144 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.3391+831C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312518 | |||||||
chr1:91312533 | T | C | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3391+816A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312533 | |||||||
chr1:91312939 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3391+410G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312939 | |||||||
chr1:91312977 | G | A | 2 | a0001c0004t0001g0166 a0004c0011t0001g0152 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3391+372C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91312977 | |||||||
chr1:91313064 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3391+285A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91313064 | |||||||
chr1:91313250 | A | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+99T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91313250 | |||||||
chr1:91313271 | G | GCAGT | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+74_3391+77dup others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 30/38 | chr1 | 91313271 | |||||||
chr1:91313646 | T | C | 176 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
177 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.3245-151A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 29/38 | chr1 | 91313646 | |||||||
chr1:91313792 | T | C | 1 | a0001c0002t0001g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3244+165A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 29/38 | chr1 | 91313792 | |||||||
chr1:91314073 | A | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | NA18942.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3141-13T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314073 | |||||||
chr1:91314196 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3141-136T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314196 | |||||||
chr1:91314214 | T | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3141-154A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314214 | |||||||
chr1:91314370 | C | T | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.3141-310G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314370 | |||||||
chr1:91314508 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3141-448A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314508 | |||||||
chr1:91314569 | T | A | 1 | a0001c0001t0001g0354 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3141-509A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314569 | |||||||
chr1:91314593 | A | G | 3 | a0002c0003t0001g0324 a0002c0003t0001g0325 a0002c0003t0001g0326 |
3 | HG00639.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3141-533T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314593 | |||||||
chr1:91314689 | T | C | 1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3141-629A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314689 | |||||||
chr1:91314792 | A | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3141-732T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314792 | |||||||
chr1:91314845 | T | C | 2 | a0001c0002t0001g0024 a0001c0002t0001g0027 |
2 | NA18973.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3141-785A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314845 | |||||||
chr1:91314851 | A | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.3141-791T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91314851 | |||||||
chr1:91315289 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.3140+526G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91315289 | |||||||
chr1:91315359 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(264): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.3140+456T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 28/38 | chr1 | 91315359 | |||||||
chr1:91316013 | T | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 |
3 | NA18955.hp2 NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2983-41A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 27/38 | chr1 | 91316013 | |||||||
chr1:91316019 | C | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2983-47G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 27/38 | chr1 | 91316019 | |||||||
chr1:91316087 | C | G | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2982+14G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 27/38 | chr1 | 91316087 | |||||||
chr1:91316291 | G | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2898+100C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 26/38 | chr1 | 91316291 | |||||||
chr1:91316366 | A | G | 1 | a0001c0004t0001g0176 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2898+25T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 26/38 | chr1 | 91316366 | |||||||
chr1:91316516 | A | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2813-40T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316516 | |||||||
chr1:91316532 | A | G | 2 | a0002c0003t0001g0328 a0002c0003t0001g0329 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2813-56T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316532 | |||||||
chr1:91316546 | A | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2813-70T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316546 | |||||||
chr1:91316560 | TA | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0204 a0001c0001t0001g0229 others(4): Show |
7 | HG00642.hp2 HG00735.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2813-85delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316560 | |||||||
chr1:91316672 | GA | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2813-197delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316672 | |||||||
chr1:91316960 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2813-484G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91316960 | |||||||
chr1:91317346 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2813-870C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317346 | |||||||
chr1:91317351 | T | G | 1 | a0001c0001t0001g0273 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2813-875A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317351 | |||||||
chr1:91317355 | G | A | 81 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(78): Show |
83 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2813-879C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317355 | |||||||
chr1:91317504 | A | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2813-1028T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317504 | |||||||
chr1:91317584 | A | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2813-1108T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317584 | |||||||
chr1:91317605 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2813-1129T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317605 | |||||||
chr1:91317706 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2813-1230T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317706 | |||||||
chr1:91317782 | C | T | 1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2812+1296G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317782 | |||||||
chr1:91317784 | A | C | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2812+1294T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317784 | |||||||
chr1:91317949 | T | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2812+1129A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91317949 | |||||||
chr1:91318065 | AT | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2812+1012delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318065 | |||||||
chr1:91318070 | A | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2812+1008T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318070 | |||||||
chr1:91318198 | T | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2812+880A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318198 | |||||||
chr1:91318227 | C | G | 4 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
4 | HG01123.hp2 HG01257.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2812+851G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318227 | |||||||
chr1:91318462 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2812+616A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318462 | |||||||
chr1:91318512 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2812+566A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318512 | |||||||
chr1:91318531 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(264): Show |
269 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.2812+547T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318531 | |||||||
chr1:91318551 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(272): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2812+527T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318551 | |||||||
chr1:91318944 | T | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2812+134A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91318944 | |||||||
chr1:91319012 | T | TACTAACA others(10): Show |
1 | a0001c0001t0001g0273 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2812+49_2812+65dup others(17): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91319012 | |||||||
chr1:91319062 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2812+16A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 25/38 | chr1 | 91319062 | |||||||
chr1:91319645 | G | T | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2583-255C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91319645 | |||||||
chr1:91319781 | T | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2583-391A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91319781 | |||||||
chr1:91320026 | C | T | 172 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(169): Show |
173 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2583-636G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320026 | |||||||
chr1:91320523 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2583-1133C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320523 | |||||||
chr1:91320761 | C | T | 5 | a0001c0001t0001g0257 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG01433.hp2 HG02300.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2583-1371G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320761 | |||||||
chr1:91320803 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2583-1413C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320803 | |||||||
chr1:91320838 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2583-1448G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320838 | |||||||
chr1:91320933 | A | ATGGTC | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00408.hp2 HG00438.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2583-1544_2583-154 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320933 | |||||||
chr1:91320934 | C | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00408.hp2 HG00438.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2583-1544G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320934 | |||||||
chr1:91320935 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2583-1545C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91320935 | |||||||
chr1:91321022 | C | T | 19 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2583-1632G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91321022 | |||||||
chr1:91321138 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2583-1748A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91321138 | |||||||
chr1:91321368 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2582+1582G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91321368 | |||||||
chr1:91321408 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2582+1542G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91321408 | |||||||
chr1:91321782 | C | A | 81 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(78): Show |
83 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2582+1168G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91321782 | |||||||
chr1:91322055 | T | C | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2582+895A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322055 | |||||||
chr1:91322071 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(86): Show |
90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.2582+879A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322071 | |||||||
chr1:91322118 | G | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(172): Show |
176 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.2582+832C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322118 | |||||||
chr1:91322121 | G | T | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2582+829C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322121 | |||||||
chr1:91322166 | A | G | 2 | a0002c0003t0001g0003 a0002c0003t0001g0178 |
3 | HG00280.hp1 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2582+784T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322166 | |||||||
chr1:91322270 | A | G | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2582+680T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322270 | |||||||
chr1:91322307 | C | A | 1 | a0001c0005t0002g0144 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2582+643G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322307 | |||||||
chr1:91322365 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2582+585T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322365 | |||||||
chr1:91322426 | T | C | 83 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0002t0001g0001 others(80): Show |
85 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2582+524A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322426 | |||||||
chr1:91322554 | C | T | 1 | a0001c0005t0002g0148 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2582+396G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322554 | |||||||
chr1:91322733 | C | T | 2 | a0001c0002t0001g0037 a0001c0002t0001g0041 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.2582+217G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322733 | |||||||
chr1:91322825 | A | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2582+125T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322825 | |||||||
chr1:91322873 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2582+77A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322873 | |||||||
chr1:91322885 | AAAACAAA others(13): Show |
A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2582+45_2582+64del others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 23/38 | chr1 | 91322885 | |||||||
chr1:91323037 | T | A | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2535-40A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 22/38 | chr1 | 91323037 | |||||||
chr1:91323300 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2428-101T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91323300 | |||||||
chr1:91323796 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2428-597C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91323796 | |||||||
chr1:91323963 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2427+712A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91323963 | |||||||
chr1:91323969 | A | G | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2427+706T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91323969 | |||||||
chr1:91323981 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2427+694G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91323981 | |||||||
chr1:91324071 | A | T | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2427+604T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324071 | |||||||
chr1:91324102 | T | C | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2427+573A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324102 | |||||||
chr1:91324103 | G | A | 1 | a0002c0003t0001g0323 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2427+572C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324103 | |||||||
chr1:91324142 | A | G | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2427+533T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324142 | |||||||
chr1:91324324 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2427+351T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324324 | |||||||
chr1:91324583 | T | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2427+92A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 21/38 | chr1 | 91324583 | |||||||
chr1:91324804 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2336-38G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91324804 | |||||||
chr1:91324853 | G | A | 1 | a0002c0003t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2336-87C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91324853 | |||||||
chr1:91325087 | A | ACCTGC | 19 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2336-326_2336-322d others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325087 | |||||||
chr1:91325169 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2336-403C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325169 | |||||||
chr1:91325334 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2336-568G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325334 | |||||||
chr1:91325588 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2336-822T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325588 | |||||||
chr1:91325887 | C | A | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2336-1121G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325887 | |||||||
chr1:91325942 | A | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2336-1176T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91325942 | |||||||
chr1:91326039 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0001g0350 |
3 | HG02074.hp1 HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2336-1273T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326039 | |||||||
chr1:91326049 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2336-1283T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326049 | |||||||
chr1:91326089 | A | T | 1 | a0001c0004t0001g0167 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2336-1323T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326089 | |||||||
chr1:91326330 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2336-1564G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326330 | |||||||
chr1:91326390 | A | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(174): Show |
178 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.2336-1624T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326390 | |||||||
chr1:91326474 | GA | G | 10 | a0001c0001t0001g0208 a0001c0005t0002g0144 a0001c0005t0002g0145 others(7): Show |
10 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.2336-1709delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326474 | |||||||
chr1:91326496 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2336-1730A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326496 | |||||||
chr1:91326639 | A | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(124): Show |
128 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2336-1873T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326639 | |||||||
chr1:91326657 | G | A | 27 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(24): Show |
28 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2336-1891C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91326657 | |||||||
chr1:91327096 | G | A | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2336-2330C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327096 | |||||||
chr1:91327200 | G | A | 2 | a0001c0004t0001g0171 a0001c0004t0001g0172 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2336-2434C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327200 | |||||||
chr1:91327401 | C | G | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2336-2635G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327401 | |||||||
chr1:91327587 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2336-2821C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327587 | |||||||
chr1:91327872 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0121 |
3 | HG02080.hp1 NA19080.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2336-3106C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327872 | |||||||
chr1:91327911 | T | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2336-3145A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327911 | |||||||
chr1:91327958 | A | G | 2 | a0003c0012t0001g0142 a0004c0011t0001g0152 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2336-3192T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91327958 | |||||||
chr1:91328179 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2336-3413A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328179 | |||||||
chr1:91328209 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2336-3443G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328209 | |||||||
chr1:91328529 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2336-3763C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328529 | |||||||
chr1:91328534 | G | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
125 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.2336-3768C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328534 | |||||||
chr1:91328691 | G | A | 151 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(148): Show |
152 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.2336-3925C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328691 | |||||||
chr1:91328703 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2336-3937C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328703 | |||||||
chr1:91328739 | G | A | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2336-3973C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328739 | |||||||
chr1:91328850 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2336-4084T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328850 | |||||||
chr1:91328912 | C | T | 11 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2336-4146G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328912 | |||||||
chr1:91328937 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
125 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2336-4171C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91328937 | |||||||
chr1:91329187 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2336-4421G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329187 | |||||||
chr1:91329307 | T | G | 1 | a0001c0004t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2336-4541A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329307 | |||||||
chr1:91329508 | A | C | 22 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(19): Show |
22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.2336-4742T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329508 | |||||||
chr1:91329549 | C | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2336-4783G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329549 | |||||||
chr1:91329857 | G | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2336-5091C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329857 | |||||||
chr1:91329910 | G | A | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG02559.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2336-5144C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91329910 | |||||||
chr1:91330190 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2336-5424G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330190 | |||||||
chr1:91330289 | A | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2336-5523T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330289 | |||||||
chr1:91330442 | G | C | 1 | a0002c0003t0001g0338 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2336-5676C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330442 | |||||||
chr1:91330483 | A | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2336-5717T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330483 | |||||||
chr1:91330686 | CAA | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2336-5922_2336-592 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330686 | |||||||
chr1:91330838 | A | G | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2336-6072T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330838 | |||||||
chr1:91330847 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2336-6081G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330847 | |||||||
chr1:91330877 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2336-6111A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91330877 | |||||||
chr1:91331039 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2336-6273G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331039 | |||||||
chr1:91331062 | T | C | 1 | a0004c0008t0001g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2336-6296A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331062 | |||||||
chr1:91331187 | A | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2336-6421T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331187 | |||||||
chr1:91331307 | G | C | 1 | a0001c0002t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2336-6541C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331307 | |||||||
chr1:91331675 | C | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | NA18977.hp1 NA18991.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2336-6909G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331675 | |||||||
chr1:91331707 | C | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2336-6941G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331707 | |||||||
chr1:91331716 | C | T | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2336-6950G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331716 | |||||||
chr1:91331746 | A | C | 52 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(49): Show |
53 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2336-6980T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331746 | |||||||
chr1:91331753 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0226 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2336-6987C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331753 | |||||||
chr1:91331850 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2336-7084G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331850 | |||||||
chr1:91331874 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2336-7108G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91331874 | |||||||
chr1:91332022 | A | T | 35 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0201 others(32): Show |
35 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.2336-7256T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332022 | |||||||
chr1:91332023 | T | C | 1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2336-7257A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332023 | |||||||
chr1:91332025 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2336-7259A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332025 | |||||||
chr1:91332152 | G | C | 1 | a0001c0001t0001g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2336-7386C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332152 | |||||||
chr1:91332168 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0001g0259 a0001c0001t0001g0270 others(4): Show |
7 | HG00544.hp2 NA18941.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.2336-7402G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332168 | |||||||
chr1:91332185 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2336-7419G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332185 | |||||||
chr1:91332252 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2336-7486G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332252 | |||||||
chr1:91332436 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2336-7670A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332436 | |||||||
chr1:91332517 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.2336-7751C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332517 | |||||||
chr1:91332570 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2336-7804G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332570 | |||||||
chr1:91332784 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(293): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2336-8018C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332784 | |||||||
chr1:91332821 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2336-8055A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91332821 | |||||||
chr1:91333253 | T | C | 1 | a0001c0004t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2336-8487A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91333253 | |||||||
chr1:91333511 | T | TA | 12 | a0001c0001t0001g0349 a0001c0002t0005g0052 a0002c0003t0001g0003 others(9): Show |
13 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2336-8746dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91333511 | |||||||
chr1:91333568 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0254 |
2 | HG03471.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2336-8802G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91333568 | |||||||
chr1:91333660 | G | A | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2336-8894C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91333660 | |||||||
chr1:91334065 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2336-9299G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334065 | |||||||
chr1:91334203 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2335+9227T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334203 | |||||||
chr1:91334553 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2335+8877C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334553 | |||||||
chr1:91334582 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2335+8848T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334582 | |||||||
chr1:91334592 | G | A | 7 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG02258.hp2 NA18946.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.2335+8838C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334592 | |||||||
chr1:91334653 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2335+8777C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334653 | |||||||
chr1:91334656 | C | A | 1 | a0001c0004t0001g0174 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2335+8774G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334656 | |||||||
chr1:91334726 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2335+8704G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334726 | |||||||
chr1:91334780 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2335+8650A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334780 | |||||||
chr1:91334790 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(293): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2335+8640C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334790 | |||||||
chr1:91334821 | C | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2335+8609G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334821 | |||||||
chr1:91334854 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2335+8576C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334854 | |||||||
chr1:91334875 | G | A | 27 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(24): Show |
28 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.2335+8555C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334875 | |||||||
chr1:91334930 | C | CA | 11 | a0001c0001t0001g0130 a0001c0001t0001g0267 a0001c0004t0001g0167 others(8): Show |
11 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.2335+8499dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91334930 | |||||||
chr1:91335389 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.2335+8041T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335389 | |||||||
chr1:91335617 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2335+7813A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335617 | |||||||
chr1:91335748 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2335+7682A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335748 | |||||||
chr1:91335769 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2335+7661T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335769 | |||||||
chr1:91335886 | G | A | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2335+7544C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335886 | |||||||
chr1:91335909 | C | A | 1 | a0003c0009t0001g0345 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2335+7521G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335909 | |||||||
chr1:91335991 | T | C | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2335+7439A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91335991 | |||||||
chr1:91336234 | CCCTCCCT others(5): Show |
C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2335+7184_2335+719 others(16): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336234 | |||||||
chr1:91336567 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2335+6863C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336567 | |||||||
chr1:91336590 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.2335+6840C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336590 | |||||||
chr1:91336653 | C | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+6777G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336653 | |||||||
chr1:91336709 | G | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2335+6721C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336709 | |||||||
chr1:91336739 | C | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(147): Show |
151 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2335+6691G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336739 | |||||||
chr1:91336754 | T | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+6676A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336754 | |||||||
chr1:91336948 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2335+6482C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91336948 | |||||||
chr1:91337195 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2335+6235G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337195 | |||||||
chr1:91337226 | A | C | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2335+6204T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337226 | |||||||
chr1:91337235 | G | A | 1 | a0001c0004t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2335+6195C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337235 | |||||||
chr1:91337244 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0227 a0001c0001t0001g0297 |
3 | NA18942.hp2 NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2335+6186A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337244 | |||||||
chr1:91337389 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2335+6041C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337389 | |||||||
chr1:91337412 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2335+6018T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337412 | |||||||
chr1:91337484 | A | G | 52 | a0001c0001t0001g0238 a0001c0002t0001g0001 a0001c0002t0001g0005 others(49): Show |
53 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2335+5946T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337484 | |||||||
chr1:91337521 | A | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2335+5909T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337521 | |||||||
chr1:91337626 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+5804G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337626 | |||||||
chr1:91337627 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG00438.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2335+5803C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337627 | |||||||
chr1:91337753 | G | A | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2335+5677C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337753 | |||||||
chr1:91337918 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2335+5512T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91337918 | |||||||
chr1:91338109 | G | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2335+5321C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338109 | |||||||
chr1:91338124 | C | T | 11 | a0001c0002t0001g0020 a0002c0003t0001g0321 a0002c0003t0001g0322 others(8): Show |
11 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2335+5306G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338124 | |||||||
chr1:91338125 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2335+5305C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338125 | |||||||
chr1:91338260 | G | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2335+5170C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338260 | |||||||
chr1:91338276 | G | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2335+5154C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338276 | |||||||
chr1:91338347 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2335+5083G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338347 | |||||||
chr1:91338550 | G | A | 2 | a0001c0001t0001g0238 a0001c0002t0001g0009 |
2 | HG00438.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2335+4880C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338550 | |||||||
chr1:91338657 | TC | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2335+4772delG | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338657 | |||||||
chr1:91338796 | C | G | 49 | a0001c0001t0001g0238 a0001c0002t0001g0001 a0001c0002t0001g0005 others(46): Show |
50 | HG00323.hp2 HG00438.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2335+4634G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338796 | |||||||
chr1:91338811 | C | G | 1 | a0001c0002t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2335+4619G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338811 | |||||||
chr1:91338866 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2335+4564C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338866 | |||||||
chr1:91338896 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2335+4534T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91338896 | |||||||
chr1:91339217 | T | G | 1 | a0001c0001t0001g0081 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2335+4213A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339217 | |||||||
chr1:91339318 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(87): Show |
91 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.2335+4112T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339318 | |||||||
chr1:91339450 | C | T | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2335+3980G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339450 | |||||||
chr1:91339486 | G | C | 1 | a0001c0001t0001g0228 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2335+3944C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339486 | |||||||
chr1:91339569 | C | T | 1 | a0002c0003t0001g0330 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2335+3861G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339569 | |||||||
chr1:91339833 | C | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2335+3597G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339833 | |||||||
chr1:91339986 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2335+3444G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91339986 | |||||||
chr1:91340017 | A | AT | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+3412dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340017 | |||||||
chr1:91340192 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+3238A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340192 | |||||||
chr1:91340505 | C | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+2925G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340505 | |||||||
chr1:91340791 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2335+2639G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340791 | |||||||
chr1:91340813 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2335+2617T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340813 | |||||||
chr1:91340835 | A | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
4 | NA18941.hp2 NA18944.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.2335+2595T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340835 | |||||||
chr1:91340838 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2335+2592T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340838 | |||||||
chr1:91340879 | C | G | 1 | a0001c0004t0001g0165 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2335+2551G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91340879 | |||||||
chr1:91341016 | A | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2335+2414T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341016 | |||||||
chr1:91341319 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2335+2111A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341319 | |||||||
chr1:91341442 | G | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2335+1988C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341442 | |||||||
chr1:91341470 | C | T | 6 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0026 others(3): Show |
6 | NA18954.hp1 NA18973.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.2335+1960G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341470 | |||||||
chr1:91341545 | A | G | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2335+1885T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341545 | |||||||
chr1:91341779 | CA | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2335+1650delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341779 | |||||||
chr1:91341789 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2335+1641T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91341789 | |||||||
chr1:91342129 | C | T | 1 | a0002c0003t0001g0348 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2335+1301G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342129 | |||||||
chr1:91342151 | A | AAAAAC | 108 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(105): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2335+1278_2335+127 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342151 | |||||||
chr1:91342151 | A | AAAC | 18 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(15): Show |
18 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2335+1278_2335+127 others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342151 | |||||||
chr1:91342159 | G | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2335+1271C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342159 | |||||||
chr1:91342181 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2335+1249A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342181 | |||||||
chr1:91342246 | G | A | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.2335+1184C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342246 | |||||||
chr1:91342292 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2335+1138G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342292 | |||||||
chr1:91342439 | G | A | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2335+991C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342439 | |||||||
chr1:91342634 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2335+796G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342634 | |||||||
chr1:91342934 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2335+496G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91342934 | |||||||
chr1:91343010 | A | T | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2335+420T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343010 | |||||||
chr1:91343054 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2335+376G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343054 | |||||||
chr1:91343104 | G | A | 1 | a0001c0002t0001g0027 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2335+326C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343104 | |||||||
chr1:91343117 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2335+313C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343117 | |||||||
chr1:91343124 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2335+306C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343124 | |||||||
chr1:91343230 | C | CA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(90): Show |
95 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.2335+199dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343230 | |||||||
chr1:91343230 | C | CAA | 163 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(160): Show |
164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2335+198_2335+199d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343230 | |||||||
chr1:91343230 | C | CAAA | 66 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(63): Show |
66 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.2335+197_2335+199d others(5): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343230 | |||||||
chr1:91343230 | C | CAAAAA | 24 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(21): Show |
25 | HG00280.hp1 HG00639.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2335+195_2335+199d others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343230 | |||||||
chr1:91343230 | C | CAAAAAA | 6 | a0002c0003t0001g0327 a0002c0003t0001g0329 a0002c0003t0001g0338 others(3): Show |
6 | HG01069.hp2 HG01081.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.2335+194_2335+199d others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343230 | |||||||
chr1:91343317 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2335+113C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343317 | |||||||
chr1:91343385 | T | C | 1 | a0001c0002t0005g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2335+45A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 20/38 | chr1 | 91343385 | |||||||
chr1:91343575 | T | C | 1 | a0001c0004t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2255-65A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91343575 | |||||||
chr1:91344072 | T | C | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2255-562A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344072 | |||||||
chr1:91344075 | A | C | 21 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(18): Show |
21 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.2255-565T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344075 | |||||||
chr1:91344146 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2255-636G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344146 | |||||||
chr1:91344156 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2255-646G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344156 | |||||||
chr1:91344207 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2255-697G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344207 | |||||||
chr1:91344467 | A | G | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.2255-957T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344467 | |||||||
chr1:91344507 | A | G | 7 | a0001c0002t0001g0018 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
7 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.2255-997T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344507 | |||||||
chr1:91344595 | A | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2255-1085T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344595 | |||||||
chr1:91344753 | G | GTT | 56 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(53): Show |
57 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.2255-1245_2255-124 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344753 | |||||||
chr1:91344753 | G | GTTT | 6 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0026 others(3): Show |
6 | NA18954.hp1 NA18973.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.2255-1246_2255-124 others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344753 | |||||||
chr1:91344923 | T | A | 10 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0260 others(7): Show |
10 | HG01255.hp2 HG01346.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.2255-1413A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91344923 | |||||||
chr1:91345026 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2255-1516C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345026 | |||||||
chr1:91345048 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2255-1538A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345048 | |||||||
chr1:91345151 | C | A | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2255-1641G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345151 | |||||||
chr1:91345545 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2254+1884C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345545 | |||||||
chr1:91345678 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2254+1751A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345678 | |||||||
chr1:91345711 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2254+1718T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345711 | |||||||
chr1:91345955 | C | A | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2254+1474G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345955 | |||||||
chr1:91345977 | G | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2254+1452C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91345977 | |||||||
chr1:91346007 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2254+1422G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346007 | |||||||
chr1:91346035 | A | C | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.2254+1394T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346035 | |||||||
chr1:91346120 | CT | C | 114 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
115 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2254+1308delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346120 | |||||||
chr1:91346165 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2254+1264A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346165 | |||||||
chr1:91346290 | A | C | 2 | a0001c0002t0001g0037 a0001c0002t0001g0041 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.2254+1139T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346290 | |||||||
chr1:91346756 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2254+673A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91346756 | |||||||
chr1:91347051 | A | G | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2254+378T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91347051 | |||||||
chr1:91347423 | T | C | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.2254+6A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 19/38 | chr1 | 91347423 | |||||||
chr1:91347600 | T | G | 1 | a0001c0005t0002g0149 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2207-124A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91347600 | |||||||
chr1:91347824 | A | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2207-348T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91347824 | |||||||
chr1:91347898 | C | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(124): Show |
128 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2207-422G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91347898 | |||||||
chr1:91348069 | G | A | 1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2207-593C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348069 | |||||||
chr1:91348162 | C | T | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(302): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.2207-686G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348162 | |||||||
chr1:91348217 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2207-741A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348217 | |||||||
chr1:91348526 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2207-1050G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348526 | |||||||
chr1:91348561 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2207-1085G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348561 | |||||||
chr1:91348642 | A | G | 1 | a0001c0002t0001g0037 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2207-1166T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348642 | |||||||
chr1:91348656 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2207-1180T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348656 | |||||||
chr1:91348808 | C | T | 208 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(205): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.2207-1332G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348808 | |||||||
chr1:91348996 | T | C | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.2207-1520A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91348996 | |||||||
chr1:91349269 | T | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2206+1469A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349269 | |||||||
chr1:91349285 | CA | C | 265 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(262): Show |
268 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2206+1452delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349285 | |||||||
chr1:91349285 | CAA | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(82): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.2206+1451_2206+145 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349285 | |||||||
chr1:91349832 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2206+906C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349832 | |||||||
chr1:91349861 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02559.hp1 HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2206+877T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349861 | |||||||
chr1:91349968 | A | C | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2206+770T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91349968 | |||||||
chr1:91350321 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2206+417A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 18/38 | chr1 | 91350321 | |||||||
chr1:91350932 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.2073-61T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 17/38 | chr1 | 91350932 | |||||||
chr1:91351068 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2073-197A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 17/38 | chr1 | 91351068 | |||||||
chr1:91351316 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2072+233A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 17/38 | chr1 | 91351316 | |||||||
chr1:91351428 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2072+121T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 17/38 | chr1 | 91351428 | |||||||
chr1:91352228 | TA | T | 6 | a0001c0001t0001g0217 a0001c0001t0001g0353 a0002c0003t0001g0003 others(3): Show |
7 | HG00280.hp1 HG00741.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1977+277delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 16/38 | chr1 | 91352228 | |||||||
chr1:91352229 | A | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1977+277T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 16/38 | chr1 | 91352229 | |||||||
chr1:91352312 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1977+194T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 16/38 | chr1 | 91352312 | |||||||
chr1:91352354 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1977+152A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 16/38 | chr1 | 91352354 | |||||||
chr1:91352745 | A | G | 22 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(19): Show |
22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1832-94T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 15/38 | chr1 | 91352745 | |||||||
chr1:91353204 | C | T | 3 | a0001c0016t0001g0141 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | HG02886.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1729+52G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 14/38 | chr1 | 91353204 | |||||||
chr1:91353448 | C | T | 1 | a0003c0009t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1686-149G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353448 | |||||||
chr1:91353530 | C | T | 3 | a0002c0003t0001g0340 a0002c0003t0001g0341 a0002c0003t0001g0348 |
3 | HG01106.hp2 HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1686-231G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353530 | |||||||
chr1:91353617 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1686-318G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353617 | |||||||
chr1:91353651 | G | GC | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(140): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1686-353dupG | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353651 | |||||||
chr1:91353652 | C | CCA | 15 | a0001c0001t0001g0111 a0001c0001t0001g0185 a0001c0001t0001g0200 others(12): Show |
15 | HG01433.hp2 HG02818.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.1686-354_1686-353i others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353652 | |||||||
chr1:91353652 | C | CCAA | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0004t0001g0166 |
3 | HG01891.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1686-354_1686-353i others(5): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353652 | |||||||
chr1:91353652 | CA | C | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(22): Show |
25 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1686-354delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353652 | |||||||
chr1:91353652 | CAA | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0008 others(39): Show |
43 | HG00323.hp2 HG00735.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1686-355_1686-354d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353652 | |||||||
chr1:91353653 | A | C | 125 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(122): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1686-354T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353653 | |||||||
chr1:91353654 | A | C | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(22): Show |
25 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1686-355T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353654 | |||||||
chr1:91353655 | A | C | 42 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0008 others(39): Show |
43 | HG00323.hp2 HG00735.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1686-356T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353655 | |||||||
chr1:91353656 | A | C | 3 | a0001c0002t0001g0007 a0004c0008t0001g0318 a0004c0008t0001g0319 |
3 | NA18965.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1686-357T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353656 | |||||||
chr1:91353666 | A | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1686-367T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353666 | |||||||
chr1:91353876 | T | C | 7 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | NA18954.hp2 NA18970.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1686-577A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353876 | |||||||
chr1:91353894 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1686-595T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353894 | |||||||
chr1:91353922 | T | TA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1686-624_1686-623i others(3): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353922 | |||||||
chr1:91353922 | TG | T | 150 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
151 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1686-624delC | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353922 | |||||||
chr1:91353923 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1686-624C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353923 | |||||||
chr1:91353923 | G | GA | 8 | a0001c0002t0001g0039 a0001c0005t0002g0144 a0001c0005t0002g0145 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1686-625dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353923 | |||||||
chr1:91353978 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1686-679C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91353978 | |||||||
chr1:91354195 | C | A | 1 | a0001c0004t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1686-896G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354195 | |||||||
chr1:91354321 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1686-1022T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354321 | |||||||
chr1:91354506 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1686-1207G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354506 | |||||||
chr1:91354517 | A | C | 22 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(19): Show |
22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.1686-1218T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354517 | |||||||
chr1:91354557 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1686-1258T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354557 | |||||||
chr1:91354889 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1686-1590G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91354889 | |||||||
chr1:91355071 | G | A | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.1686-1772C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355071 | |||||||
chr1:91355077 | A | G | 3 | a0001c0002t0001g0007 a0001c0002t0001g0008 a0001c0002t0001g0011 |
3 | NA18944.hp2 NA18965.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1686-1778T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355077 | |||||||
chr1:91355144 | A | G | 1 | a0001c0005t0002g0144 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1686-1845T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355144 | |||||||
chr1:91355216 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1686-1917A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355216 | |||||||
chr1:91355311 | C | G | 1 | a0001c0002t0001g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1686-2012G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355311 | |||||||
chr1:91355432 | G | GA | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1686-2134dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355432 | |||||||
chr1:91355484 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1686-2185A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355484 | |||||||
chr1:91355585 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1686-2286T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355585 | |||||||
chr1:91355636 | C | T | 18 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(15): Show |
18 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1686-2337G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355636 | |||||||
chr1:91355672 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1686-2373A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355672 | |||||||
chr1:91355697 | T | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1686-2398A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355697 | |||||||
chr1:91355751 | C | T | 1 | a0001c0004t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1686-2452G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355751 | |||||||
chr1:91355946 | A | G | 210 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(207): Show |
212 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1686-2647T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91355946 | |||||||
chr1:91356023 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1686-2724A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356023 | |||||||
chr1:91356160 | A | G | 6 | a0001c0001t0001g0245 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG02074.hp2 HG02080.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1686-2861T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356160 | |||||||
chr1:91356244 | AT | A | 16 | a0001c0001t0001g0203 a0001c0001t0001g0211 a0001c0001t0001g0292 others(13): Show |
16 | HG01070.hp1 HG01070.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1686-2946delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356244 | |||||||
chr1:91356441 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(81): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1686-3142G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356441 | |||||||
chr1:91356487 | A | G | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1686-3188T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356487 | |||||||
chr1:91356540 | C | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1686-3241G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356540 | |||||||
chr1:91356588 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1686-3289T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356588 | |||||||
chr1:91356642 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1686-3343T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356642 | |||||||
chr1:91356825 | A | G | 156 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(153): Show |
157 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1686-3526T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356825 | |||||||
chr1:91356933 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1686-3634A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91356933 | |||||||
chr1:91357411 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1686-4112C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357411 | |||||||
chr1:91357581 | A | G | 2 | a0003c0009t0001g0197 a0003c0013t0001g0143 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1686-4282T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357581 | |||||||
chr1:91357619 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1686-4320C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357619 | |||||||
chr1:91357786 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1686-4487C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357786 | |||||||
chr1:91357919 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1686-4620A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357919 | |||||||
chr1:91357963 | A | G | 1 | a0001c0004t0001g0170 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1686-4664T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91357963 | |||||||
chr1:91358240 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1686-4941G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358240 | |||||||
chr1:91358283 | C | CA | 52 | a0001c0001t0001g0112 a0001c0002t0001g0001 a0001c0002t0001g0005 others(49): Show |
53 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.1686-4985dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358283 | |||||||
chr1:91358294 | T | A | 303 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(300): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1686-4995A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358294 | |||||||
chr1:91358399 | A | G | 2 | a0003c0009t0001g0197 a0003c0013t0001g0143 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1686-5100T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358399 | |||||||
chr1:91358564 | A | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA18972.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1686-5265T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358564 | |||||||
chr1:91358829 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1686-5530C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91358829 | |||||||
chr1:91359068 | C | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(298): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1686-5769G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359068 | |||||||
chr1:91359255 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1686-5956A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359255 | |||||||
chr1:91359310 | G | A | 1 | a0001c0004t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1686-6011C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359310 | |||||||
chr1:91359341 | A | G | 7 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | NA18954.hp2 NA18970.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1686-6042T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359341 | |||||||
chr1:91359553 | CA | C | 10 | a0001c0001t0001g0073 a0001c0001t0001g0127 a0001c0001t0001g0136 others(7): Show |
10 | HG02647.hp2 HG02698.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1686-6255delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359553 | |||||||
chr1:91359553 | CAAA | C | 6 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0200 others(3): Show |
6 | HG01257.hp2 HG01258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1686-6257_1686-625 others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359553 | |||||||
chr1:91359882 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1686-6583G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91359882 | |||||||
chr1:91360068 | T | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1686-6769A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360068 | |||||||
chr1:91360228 | C | T | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1686-6929G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360228 | |||||||
chr1:91360250 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1686-6951C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360250 | |||||||
chr1:91360327 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1686-7028G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360327 | |||||||
chr1:91360401 | T | C | 2 | a0002c0003t0001g0328 a0002c0003t0001g0329 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1686-7102A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360401 | |||||||
chr1:91360526 | G | A | 1 | a0008c0018t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1686-7227C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360526 | |||||||
chr1:91360614 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1686-7315A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360614 | |||||||
chr1:91360971 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1686-7672C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91360971 | |||||||
chr1:91361063 | T | C | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1686-7764A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361063 | |||||||
chr1:91361084 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1686-7785G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361084 | |||||||
chr1:91361189 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1686-7890C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361189 | |||||||
chr1:91361236 | CA | C | 52 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0268 others(49): Show |
53 | HG00323.hp2 HG00673.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1686-7938delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361236 | |||||||
chr1:91361302 | C | A | 1 | a0002c0003t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1686-8003G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361302 | |||||||
chr1:91361368 | G | A | 2 | a0001c0002t0001g0037 a0001c0002t0001g0041 |
2 | HG00323.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.1686-8069C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361368 | |||||||
chr1:91361387 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1686-8088A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361387 | |||||||
chr1:91361772 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1686-8473A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91361772 | |||||||
chr1:91362444 | T | C | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1686-9145A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91362444 | |||||||
chr1:91362448 | T | C | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1686-9149A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91362448 | |||||||
chr1:91362715 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1686-9416T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91362715 | |||||||
chr1:91362776 | A | C | 2 | a0001c0005t0002g0145 a0001c0005t0002g0146 |
2 | HG02135.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1686-9477T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91362776 | |||||||
chr1:91363022 | T | A | 1 | a0001c0001t0001g0309 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1686-9723A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363022 | |||||||
chr1:91363141 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1686-9842G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363141 | |||||||
chr1:91363524 | C | CA | 89 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1686-10226dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363524 | |||||||
chr1:91363524 | C | CAA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0077 others(5): Show |
9 | HG00558.hp1 HG00609.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1686-10227_1686-10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363524 | |||||||
chr1:91363572 | G | C | 297 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(294): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1686-10273C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363572 | |||||||
chr1:91363620 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1686-10321C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363620 | |||||||
chr1:91363657 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1686-10358G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363657 | |||||||
chr1:91363745 | T | C | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1686-10446A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363745 | |||||||
chr1:91363994 | A | G | 13 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0001c0001t0001g0262 others(10): Show |
13 | HG00558.hp2 HG01081.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1686-10695T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91363994 | |||||||
chr1:91364034 | G | A | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1686-10735C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364034 | |||||||
chr1:91364102 | G | GA | 3 | a0001c0002t0001g0001 a0001c0002t0001g0023 a0001c0002t0001g0139 |
4 | HG02155.hp2 NA18947.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686-10804dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364102 | |||||||
chr1:91364362 | C | T | 1 | a0001c0004t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1685+10996G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364362 | |||||||
chr1:91364367 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1685+10991A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364367 | |||||||
chr1:91364607 | C | CAT | 11 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | HG00408.hp2 HG00438.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1685+10749_1685+10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364607 | |||||||
chr1:91364607 | C | CATAT | 3 | a0001c0004t0001g0166 a0003c0009t0001g0197 a0003c0013t0001g0143 |
3 | HG02280.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1685+10747_1685+10 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364607 | |||||||
chr1:91364607 | CATAT | C | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0258 others(6): Show |
9 | HG00558.hp2 HG01081.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1685+10747_1685+10 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364607 | |||||||
chr1:91364613 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1685+10745A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364613 | |||||||
chr1:91364626 | A | AT | 6 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
6 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685+10731dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364626 | |||||||
chr1:91364626 | A | ATT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0180 others(4): Show |
7 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1685+10731_1685+10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364626 | |||||||
chr1:91364626 | A | ATTT | 5 | a0001c0001t0001g0004 a0001c0001t0001g0216 a0001c0001t0001g0234 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685+10731_1685+10 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364626 | |||||||
chr1:91364626 | A | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0285 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1685+10732T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364626 | |||||||
chr1:91364628 | A | AT | 12 | a0001c0001t0001g0177 a0001c0001t0001g0202 a0001c0001t0001g0288 others(9): Show |
12 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.1685+10729dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364628 | |||||||
chr1:91364628 | A | ATT | 60 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(57): Show |
60 | HG00140.hp2 HG00642.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1685+10729_1685+10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364628 | |||||||
chr1:91364628 | A | ATTT | 5 | a0001c0001t0001g0136 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | HG02683.hp1 HG03942.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685+10729_1685+10 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364628 | |||||||
chr1:91364628 | A | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(24): Show |
28 | HG00438.hp1 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1685+10730T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364628 | |||||||
chr1:91364630 | A | AT | 24 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(21): Show |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1685+10727dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364630 | |||||||
chr1:91364630 | A | ATT | 18 | a0001c0001t0001g0132 a0001c0001t0001g0183 a0001c0001t0001g0200 others(15): Show |
18 | HG00642.hp1 HG01433.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.1685+10727_1685+10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364630 | |||||||
chr1:91364630 | A | ATTT | 5 | a0001c0001t0001g0056 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1685+10727_1685+10 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364630 | |||||||
chr1:91364630 | A | ATTTT | 6 | a0001c0001t0001g0259 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG00544.hp2 HG02280.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685+10727_1685+10 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364630 | |||||||
chr1:91364630 | A | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
116 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1685+10728T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364630 | |||||||
chr1:91364631 | TA | T | 4 | a0001c0016t0001g0141 a0002c0003t0001g0324 a0002c0003t0001g0325 others(1): Show |
4 | HG00639.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685+10726delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364631 | |||||||
chr1:91364632 | A | AT | 12 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0004t0001g0156 others(9): Show |
12 | HG00280.hp1 HG00558.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1685+10725dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATAT | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0098 others(7): Show |
10 | HG02080.hp1 HG02735.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(23): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0009 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(27): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0041 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0037 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(21): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(23): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0317 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(7): Show |
1 | a0001c0002t0001g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(5): Show |
4 | a0001c0002t0001g0019 a0001c0002t0001g0039 a0001c0002t0001g0042 others(1): Show |
4 | HG02886.hp1 NA19003.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(18): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(6): Show |
18 | a0001c0002t0001g0001 a0001c0002t0001g0022 a0001c0002t0001g0023 others(15): Show |
19 | HG01123.hp2 HG01952.hp2 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(7): Show |
7 | a0001c0002t0001g0011 a0001c0002t0001g0020 a0001c0002t0001g0021 others(4): Show |
7 | HG01928.hp1 HG06807.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(20): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(8): Show |
2 | a0001c0002t0001g0005 a0001c0002t0001g0031 |
2 | NA18955.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(21): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATAT others(9): Show |
1 | a0001c0002t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(22): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATTT others(4): Show |
1 | a0001c0002t0001g0007 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(17): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATTT others(5): Show |
1 | a0001c0002t0001g0008 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(18): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATATTT others(6): Show |
4 | a0001c0002t0001g0010 a0001c0002t0001g0030 a0001c0002t0001g0049 others(1): Show |
4 | HG01884.hp2 HG02717.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATT | 6 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG01255.hp1 HG03704.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1685+10725_1685+10 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATTTTT others(5): Show |
1 | a0001c0002t0001g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(18): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATATTTTT others(6): Show |
1 | a0001c0002t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1685+10725_1685+10 others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATT | 54 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(51): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1685+10724_1685+10 others(8): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATTT | 6 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0001g0201 others(3): Show |
6 | HG02486.hp2 HG04228.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685+10723_1685+10 others(9): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | ATTTT | 6 | a0001c0001t0001g0067 a0001c0001t0001g0090 a0001c0001t0001g0228 others(3): Show |
6 | HG01361.hp2 HG01981.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1685+10722_1685+10 others(10): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | A | T | 170 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(167): Show |
172 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.1685+10726T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364632 | AT | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0214 others(6): Show |
9 | HG01891.hp2 HG02135.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1685+10725delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364632 | |||||||
chr1:91364633 | T | TA | 3 | a0001c0001t0001g0306 a0001c0004t0001g0173 a0001c0004t0001g0176 |
3 | HG02738.hp2 HG02970.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1685+10724_1685+10 others(7): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364633 | |||||||
chr1:91364634 | T | A | 2 | a0001c0001t0001g0083 a0004c0011t0001g0152 |
2 | HG02155.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1685+10724A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364634 | |||||||
chr1:91364723 | C | G | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.1685+10635G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364723 | |||||||
chr1:91364724 | C | T | 2 | a0001c0001t0001g0306 a0002c0003t0001g0344 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1685+10634G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364724 | |||||||
chr1:91364791 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1685+10567C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364791 | |||||||
chr1:91364825 | G | C | 2 | a0003c0009t0001g0197 a0003c0013t0001g0143 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1685+10533C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364825 | |||||||
chr1:91364870 | T | C | 2 | a0003c0009t0001g0197 a0003c0013t0001g0143 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1685+10488A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364870 | |||||||
chr1:91364925 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1685+10433C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364925 | |||||||
chr1:91364950 | T | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG00642.hp1 HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1685+10408A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91364950 | |||||||
chr1:91365028 | C | T | 2 | a0004c0011t0001g0152 a0008c0018t0001g0253 |
2 | HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1685+10330G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365028 | |||||||
chr1:91365134 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1685+10224G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365134 | |||||||
chr1:91365206 | A | G | 9 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1685+10152T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365206 | |||||||
chr1:91365540 | T | C | 23 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(20): Show |
23 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1685+9818A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365540 | |||||||
chr1:91365623 | A | T | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.1685+9735T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365623 | |||||||
chr1:91365813 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1685+9545G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365813 | |||||||
chr1:91365851 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1685+9507T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365851 | |||||||
chr1:91365968 | GA | G | 262 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(259): Show |
265 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.1685+9389delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91365968 | |||||||
chr1:91366066 | C | T | 1 | a0001c0002t0001g0011 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1685+9292G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366066 | |||||||
chr1:91366072 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1685+9286C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366072 | |||||||
chr1:91366232 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1685+9126G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366232 | |||||||
chr1:91366507 | C | T | 36 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0201 others(33): Show |
36 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1685+8851G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366507 | |||||||
chr1:91366520 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1685+8838G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366520 | |||||||
chr1:91366643 | G | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1685+8715C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366643 | |||||||
chr1:91366652 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1685+8706A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366652 | |||||||
chr1:91366941 | C | T | 9 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1685+8417G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91366941 | |||||||
chr1:91367001 | C | T | 7 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | NA18954.hp2 NA18970.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1685+8357G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367001 | |||||||
chr1:91367070 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1685+8288C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367070 | |||||||
chr1:91367150 | C | T | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1685+8208G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367150 | |||||||
chr1:91367204 | C | T | 1 | a0002c0003t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1685+8154G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367204 | |||||||
chr1:91367207 | C | G | 1 | a0001c0004t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1685+8151G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367207 | |||||||
chr1:91367246 | T | C | 1 | a0002c0003t0001g0344 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1685+8112A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367246 | |||||||
chr1:91367274 | C | T | 1 | a0001c0004t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1685+8084G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367274 | |||||||
chr1:91367294 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1685+8064G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367294 | |||||||
chr1:91367388 | T | A | 1 | a0001c0004t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1685+7970A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367388 | |||||||
chr1:91367496 | T | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1685+7862A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91367496 | |||||||
chr1:91368034 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1685+7324T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368034 | |||||||
chr1:91368129 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1685+7229G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368129 | |||||||
chr1:91368204 | C | G | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1685+7154G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368204 | |||||||
chr1:91368217 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1685+7141G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368217 | |||||||
chr1:91368564 | C | A | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1685+6794G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368564 | |||||||
chr1:91368666 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1685+6692T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368666 | |||||||
chr1:91368673 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1685+6685C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368673 | |||||||
chr1:91368694 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1685+6664G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368694 | |||||||
chr1:91368741 | C | T | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1685+6617G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368741 | |||||||
chr1:91368743 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1685+6615A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368743 | |||||||
chr1:91368761 | C | A | 1 | a0001c0004t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1685+6597G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368761 | |||||||
chr1:91368878 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1685+6480A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368878 | |||||||
chr1:91368975 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1685+6383C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91368975 | |||||||
chr1:91369051 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1685+6307T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369051 | |||||||
chr1:91369058 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1685+6300T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369058 | |||||||
chr1:91369124 | A | G | 4 | a0001c0004t0001g0164 a0001c0004t0001g0165 a0001c0004t0001g0166 others(1): Show |
4 | HG02965.hp2 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685+6234T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369124 | |||||||
chr1:91369184 | G | A | 2 | a0001c0001t0001g0356 a0001c0001t0001g0357 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1685+6174C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369184 | |||||||
chr1:91369291 | T | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1685+6067A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369291 | |||||||
chr1:91369506 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1685+5852A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369506 | |||||||
chr1:91369570 | T | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1685+5788A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369570 | |||||||
chr1:91369571 | C | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1685+5787G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369571 | |||||||
chr1:91369597 | T | G | 129 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(126): Show |
130 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1685+5761A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369597 | |||||||
chr1:91369794 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1685+5564T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369794 | |||||||
chr1:91369917 | C | T | 3 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0003c0012t0001g0142 |
3 | HG02683.hp1 HG03471.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1685+5441G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91369917 | |||||||
chr1:91370036 | C | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1685+5322G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370036 | |||||||
chr1:91370043 | GAA | G | 18 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(15): Show |
18 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1685+5313_1685+531 others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370043 | |||||||
chr1:91370048 | T | C | 18 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(15): Show |
18 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1685+5310A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370048 | |||||||
chr1:91370141 | A | C | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1685+5217T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370141 | |||||||
chr1:91370166 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1685+5192C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370166 | |||||||
chr1:91370232 | G | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(124): Show |
128 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1685+5126C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370232 | |||||||
chr1:91370232 | G | T | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1685+5126C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370232 | |||||||
chr1:91370249 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1685+5109G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370249 | |||||||
chr1:91370325 | G | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.1685+5033C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370325 | |||||||
chr1:91370327 | T | C | 21 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0286 others(18): Show |
21 | HG00408.hp1 HG01928.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.1685+5031A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370327 | |||||||
chr1:91370368 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1685+4990T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370368 | |||||||
chr1:91370385 | G | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1685+4973C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370385 | |||||||
chr1:91370406 | T | C | 3 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1685+4952A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370406 | |||||||
chr1:91370425 | C | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685+4933G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370425 | |||||||
chr1:91370525 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1685+4833A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370525 | |||||||
chr1:91370526 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1685+4832C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370526 | |||||||
chr1:91370542 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1685+4816G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370542 | |||||||
chr1:91370568 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4790A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370568 | |||||||
chr1:91370573 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4785A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370573 | |||||||
chr1:91370577 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4781C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370577 | |||||||
chr1:91370580 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4778A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370580 | |||||||
chr1:91370585 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4773C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370585 | |||||||
chr1:91370588 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1685+4770A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370588 | |||||||
chr1:91370637 | C | G | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1685+4721G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370637 | |||||||
chr1:91370655 | G | T | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(302): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1685+4703C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370655 | |||||||
chr1:91370915 | A | G | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1685+4443T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370915 | |||||||
chr1:91370929 | C | G | 1 | a0001c0002t0001g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1685+4429G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91370929 | |||||||
chr1:91371027 | C | A | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1685+4331G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371027 | |||||||
chr1:91371197 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1685+4161G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371197 | |||||||
chr1:91371208 | A | C | 53 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(50): Show |
54 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.1685+4150T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371208 | |||||||
chr1:91371262 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1685+4096C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371262 | |||||||
chr1:91371571 | C | A | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1685+3787G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371571 | |||||||
chr1:91371749 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1685+3609T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371749 | |||||||
chr1:91371927 | G | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(82): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1685+3431C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371927 | |||||||
chr1:91371990 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1685+3368G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91371990 | |||||||
chr1:91372018 | A | C | 2 | a0002c0003t0001g0330 a0002c0003t0001g0331 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1685+3340T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372018 | |||||||
chr1:91372170 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1685+3188C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372170 | |||||||
chr1:91372188 | C | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(295): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1685+3170G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372188 | |||||||
chr1:91372298 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1685+3060A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372298 | |||||||
chr1:91372348 | A | T | 1 | a0002c0003t0001g0324 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1685+3010T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372348 | |||||||
chr1:91372468 | G | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1685+2890C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372468 | |||||||
chr1:91372480 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1685+2878G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372480 | |||||||
chr1:91372481 | G | A | 4 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0053 others(1): Show |
4 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1685+2877C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372481 | |||||||
chr1:91372481 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1685+2877C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372481 | |||||||
chr1:91372699 | C | T | 2 | a0002c0003t0001g0003 a0002c0003t0001g0178 |
3 | HG00280.hp1 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1685+2659G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372699 | |||||||
chr1:91372841 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1685+2517G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91372841 | |||||||
chr1:91373148 | T | TA | 144 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(141): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1685+2209dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91373148 | |||||||
chr1:91373316 | G | A | 1 | a0001c0002t0001g0039 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1685+2042C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91373316 | |||||||
chr1:91373442 | A | G | 1 | a0001c0004t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1685+1916T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91373442 | |||||||
chr1:91374155 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1685+1203T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374155 | |||||||
chr1:91374173 | C | A | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1685+1185G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374173 | |||||||
chr1:91374182 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1685+1176C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374182 | |||||||
chr1:91374226 | T | A | 1 | a0001c0001t0001g0303 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1685+1132A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374226 | |||||||
chr1:91374352 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1685+1006G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374352 | |||||||
chr1:91374386 | T | C | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1685+972A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374386 | |||||||
chr1:91374526 | T | C | 1 | a0001c0004t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1685+832A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374526 | |||||||
chr1:91374551 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1685+807C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374551 | |||||||
chr1:91374628 | T | A | 1 | a0001c0002t0001g0048 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1685+730A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374628 | |||||||
chr1:91374805 | G | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1685+553C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 13/38 | chr1 | 91374805 | |||||||
chr1:91375942 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1396-215T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91375942 | |||||||
chr1:91375957 | C | T | 1 | a0008c0018t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1396-230G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91375957 | |||||||
chr1:91376080 | C | T | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1396-353G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376080 | |||||||
chr1:91376095 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1396-368C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376095 | |||||||
chr1:91376212 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1396-485A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376212 | |||||||
chr1:91376411 | G | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1396-684C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376411 | |||||||
chr1:91376513 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1396-786T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376513 | |||||||
chr1:91376607 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(81): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1396-880C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376607 | |||||||
chr1:91376636 | A | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-909T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91376636 | |||||||
chr1:91377406 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG02040.hp2 HG02074.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395+619C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91377406 | |||||||
chr1:91377766 | T | C | 1 | a0001c0005t0002g0150 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1395+259A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91377766 | |||||||
chr1:91377841 | A | G | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1395+184T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 11/38 | chr1 | 91377841 | |||||||
chr1:91378279 | A | C | 1 | a0001c0002t0001g0139 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1237-96T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 10/38 | chr1 | 91378279 | |||||||
chr1:91378682 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1159-202C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 9/38 | chr1 | 91378682 | |||||||
chr1:91378829 | C | T | 8 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0327 others(5): Show |
9 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158+234G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 9/38 | chr1 | 91378829 | |||||||
chr1:91378859 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1158+204A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 9/38 | chr1 | 91378859 | |||||||
chr1:91379245 | A | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1007-31T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379245 | |||||||
chr1:91379258 | T | C | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.1007-44A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379258 | |||||||
chr1:91379265 | C | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-51G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379265 | |||||||
chr1:91379483 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1007-269G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379483 | |||||||
chr1:91379515 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1007-301G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379515 | |||||||
chr1:91379599 | G | C | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1007-385C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379599 | |||||||
chr1:91379669 | G | GT | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
180 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1006+434dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379669 | |||||||
chr1:91379713 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1006+391G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379713 | |||||||
chr1:91379778 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1006+326T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379778 | |||||||
chr1:91379779 | A | T | 355 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(352): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1006+325T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379779 | |||||||
chr1:91379812 | A | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+292T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 8/38 | chr1 | 91379812 | |||||||
chr1:91380279 | T | C | 4 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0022 others(1): Show |
4 | NA18980.hp1 NA18991.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-43A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 7/38 | chr1 | 91380279 | |||||||
chr1:91380552 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.874-316C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 7/38 | chr1 | 91380552 | |||||||
chr1:91380647 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.873+265C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 7/38 | chr1 | 91380647 | |||||||
chr1:91380744 | T | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.873+168A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 7/38 | chr1 | 91380744 | |||||||
chr1:91380838 | T | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+74A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 7/38 | chr1 | 91380838 | |||||||
chr1:91381181 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.803-199C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381181 | |||||||
chr1:91381634 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.803-652C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381634 | |||||||
chr1:91381669 | T | C | 1 | a0001c0002t0001g0039 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.803-687A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381669 | |||||||
chr1:91381859 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.803-877A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381859 | |||||||
chr1:91381991 | C | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1009G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381991 | |||||||
chr1:91381997 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.803-1015G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91381997 | |||||||
chr1:91382292 | T | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1310A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382292 | |||||||
chr1:91382461 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.803-1479T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382461 | |||||||
chr1:91382509 | A | C | 6 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-1527T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382509 | |||||||
chr1:91382550 | G | A | 11 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
11 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-1568C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382550 | |||||||
chr1:91382584 | G | A | 1 | a0001c0002t0001g0005 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.803-1602C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382584 | |||||||
chr1:91382622 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02129.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.803-1640T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382622 | |||||||
chr1:91382753 | C | CTGAA | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.803-1772_803-1771i others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382753 | |||||||
chr1:91382754 | A | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01069.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.803-1772T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382754 | |||||||
chr1:91382881 | A | C | 1 | a0002c0003t0003g0347 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.803-1899T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382881 | |||||||
chr1:91382883 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.803-1901A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382883 | |||||||
chr1:91382883 | T | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.803-1901A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91382883 | |||||||
chr1:91383071 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.803-2089G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383071 | |||||||
chr1:91383227 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.802+1960G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383227 | |||||||
chr1:91383275 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.802+1912C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383275 | |||||||
chr1:91383301 | G | A | 1 | a0008c0018t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+1886C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383301 | |||||||
chr1:91383376 | A | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+1811T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383376 | |||||||
chr1:91383650 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.802+1537A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383650 | |||||||
chr1:91383662 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.802+1525A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383662 | |||||||
chr1:91383720 | GT | G | 51 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(48): Show |
52 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(49): Show |
intron_variant | MODIFIER | c.802+1466delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383720 | |||||||
chr1:91383728 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802+1459A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383728 | |||||||
chr1:91383894 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.802+1293A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383894 | |||||||
chr1:91383931 | AT | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(302): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.802+1255delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91383931 | |||||||
chr1:91384206 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+981G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384206 | |||||||
chr1:91384276 | G | A | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.802+911C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384276 | |||||||
chr1:91384355 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.802+832T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384355 | |||||||
chr1:91384508 | C | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+679G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384508 | |||||||
chr1:91384594 | T | C | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.802+593A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384594 | |||||||
chr1:91384747 | CT | C | 349 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(346): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.802+439delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 6/38 | chr1 | 91384747 | |||||||
chr1:91385269 | C | CA | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.755-36dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/38 | chr1 | 91385269 | |||||||
chr1:91385288 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.755-54T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/38 | chr1 | 91385288 | |||||||
chr1:91385413 | C | G | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.754+162G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/38 | chr1 | 91385413 | |||||||
chr1:91385448 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.754+127T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/38 | chr1 | 91385448 | |||||||
chr1:91385478 | A | C | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG02486.hp1 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+97T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 5/38 | chr1 | 91385478 | |||||||
chr1:91385882 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.495-48G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91385882 | |||||||
chr1:91386125 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.495-291T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386125 | |||||||
chr1:91386294 | C | T | 3 | a0002c0003t0001g0324 a0002c0003t0001g0325 a0002c0003t0001g0326 |
3 | HG00639.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.495-460G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386294 | |||||||
chr1:91386363 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.495-529G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386363 | |||||||
chr1:91386369 | GA | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00438.hp2 NA18942.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-536delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386369 | |||||||
chr1:91386578 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.495-744G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386578 | |||||||
chr1:91386603 | A | G | 4 | a0001c0001t0001g0287 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | NA18946.hp2 NA18984.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-769T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386603 | |||||||
chr1:91386642 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.495-808C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386642 | |||||||
chr1:91386699 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.495-865G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386699 | |||||||
chr1:91386709 | TATTTAA | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.495-881_495-876del others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386709 | |||||||
chr1:91386964 | G | A | 6 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-1130C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91386964 | |||||||
chr1:91387050 | C | T | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.495-1216G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387050 | |||||||
chr1:91387058 | C | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02647.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.495-1224G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387058 | |||||||
chr1:91387092 | G | A | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.495-1258C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387092 | |||||||
chr1:91387129 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA19058.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.495-1295A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387129 | |||||||
chr1:91387266 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495-1432A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387266 | |||||||
chr1:91387300 | C | T | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(302): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.495-1466G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387300 | |||||||
chr1:91387303 | C | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.495-1469G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387303 | |||||||
chr1:91387533 | G | A | 3 | a0002c0003t0001g0340 a0002c0003t0001g0341 a0002c0003t0001g0348 |
3 | HG01106.hp2 HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.495-1699C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387533 | |||||||
chr1:91387539 | G | A | 30 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.495-1705C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387539 | |||||||
chr1:91387553 | C | G | 1 | a0001c0004t0001g0163 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.495-1719G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387553 | |||||||
chr1:91387595 | G | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495-1761C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387595 | |||||||
chr1:91387708 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.495-1874A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387708 | |||||||
chr1:91387775 | G | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.495-1941C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387775 | |||||||
chr1:91387825 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495-1991C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387825 | |||||||
chr1:91387917 | TA | T | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(24): Show |
27 | HG01070.hp2 HG01074.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.495-2084delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387917 | |||||||
chr1:91387918 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0300 |
2 | HG04228.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.495-2084T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387918 | |||||||
chr1:91387919 | A | T | 1 | a0001c0004t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495-2085T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387919 | |||||||
chr1:91387931 | TA | T | 54 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0186 others(51): Show |
55 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.495-2098delT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387931 | |||||||
chr1:91387931 | TAA | T | 47 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(44): Show |
48 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.495-2099_495-2098d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387931 | |||||||
chr1:91387932 | A | T | 2 | a0001c0001t0001g0119 a0001c0005t0002g0151 |
2 | HG03704.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.495-2098T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387932 | |||||||
chr1:91387955 | AAAAC | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0002c0003t0001g0342 |
3 | HG02895.hp1 HG02897.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.495-2125_495-2122d others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91387955 | |||||||
chr1:91388073 | A | G | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.495-2239T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388073 | |||||||
chr1:91388256 | C | T | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.495-2422G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388256 | |||||||
chr1:91388464 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.495-2630A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388464 | |||||||
chr1:91388700 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.495-2866A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388700 | |||||||
chr1:91388741 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.495-2907G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388741 | |||||||
chr1:91388826 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.495-2992G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388826 | |||||||
chr1:91388832 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(289): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.495-2998C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388832 | |||||||
chr1:91388852 | T | A | 1 | a0001c0002t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.495-3018A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91388852 | |||||||
chr1:91389097 | T | C | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.495-3263A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389097 | |||||||
chr1:91389103 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0290 a0001c0001t0001g0291 others(2): Show |
5 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.495-3269G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389103 | |||||||
chr1:91389126 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.495-3292A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389126 | |||||||
chr1:91389132 | GT | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.495-3299delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389132 | |||||||
chr1:91389132 | GTT | G | 70 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0119 others(67): Show |
71 | HG00280.hp1 HG00558.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.495-3300_495-3299d others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389132 | |||||||
chr1:91389152 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.495-3318A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389152 | |||||||
chr1:91389192 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.495-3358G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389192 | |||||||
chr1:91389230 | C | T | 3 | a0002c0003t0001g0321 a0002c0003t0001g0322 a0002c0003t0001g0323 |
3 | HG02572.hp2 HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.495-3396G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389230 | |||||||
chr1:91389232 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(205): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.495-3398C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389232 | |||||||
chr1:91389248 | G | A | 22 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(19): Show |
22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.495-3414C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389248 | |||||||
chr1:91389307 | G | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.495-3473C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389307 | |||||||
chr1:91389324 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0122 others(1): Show |
4 | NA18970.hp1 NA19007.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-3490C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389324 | |||||||
chr1:91389406 | C | T | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(302): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.495-3572G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389406 | |||||||
chr1:91389428 | G | C | 13 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-3594C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389428 | |||||||
chr1:91389459 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.495-3625A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389459 | |||||||
chr1:91389598 | G | A | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.495-3764C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389598 | |||||||
chr1:91389810 | C | A | 2 | a0004c0008t0001g0318 a0004c0008t0001g0319 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.495-3976G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389810 | |||||||
chr1:91389938 | G | C | 9 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.495-4104C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91389938 | |||||||
chr1:91390106 | A | G | 6 | a0001c0007t0001g0188 a0001c0007t0001g0190 a0001c0007t0001g0193 others(3): Show |
6 | HG00609.hp1 NA18943.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+3987T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390106 | |||||||
chr1:91390243 | C | G | 131 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(128): Show |
132 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.494+3850G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390243 | |||||||
chr1:91390293 | G | A | 1 | a0004c0011t0001g0152 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.494+3800C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390293 | |||||||
chr1:91390305 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.494+3788C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390305 | |||||||
chr1:91390323 | C | T | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.494+3770G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390323 | |||||||
chr1:91390431 | C | CA | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(308): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.494+3661dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390431 | |||||||
chr1:91390434 | A | AAG | 19 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(16): Show |
19 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.494+3658_494+3659i others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390434 | |||||||
chr1:91390435 | G | A | 45 | a0001c0001t0001g0073 a0001c0001t0001g0177 a0001c0001t0001g0179 others(42): Show |
45 | HG01070.hp2 HG01074.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.494+3658C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390435 | |||||||
chr1:91390436 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0199 a0001c0001t0001g0354 |
3 | HG02683.hp1 NA19075.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.494+3657T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390436 | |||||||
chr1:91390447 | A | G | 2 | a0001c0001t0001g0287 a0001c0004t0001g0173 |
2 | HG02738.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.494+3646T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390447 | |||||||
chr1:91390458 | AAAGG | A | 27 | a0001c0001t0001g0185 a0001c0001t0001g0258 a0001c0001t0001g0259 others(24): Show |
27 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.494+3631_494+3634d others(6): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390458 | |||||||
chr1:91390501 | T | A | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.494+3592A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390501 | |||||||
chr1:91390514 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.494+3579G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390514 | |||||||
chr1:91390514 | C | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.494+3579G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390514 | |||||||
chr1:91390515 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(305): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.494+3578T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390515 | |||||||
chr1:91390524 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.494+3569G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390524 | |||||||
chr1:91390707 | C | T | 1 | a0001c0007t0001g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.494+3386G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390707 | |||||||
chr1:91390733 | T | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(175): Show |
179 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.494+3360A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390733 | |||||||
chr1:91390757 | C | T | 5 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 others(2): Show |
5 | NA18980.hp1 NA18991.hp1 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+3336G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390757 | |||||||
chr1:91390765 | T | C | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02970.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.494+3328A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390765 | |||||||
chr1:91390860 | T | C | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.494+3233A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390860 | |||||||
chr1:91390864 | C | T | 28 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(25): Show |
29 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.494+3229G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91390864 | |||||||
chr1:91391105 | C | T | 1 | a0001c0002t0001g0018 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.494+2988G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391105 | |||||||
chr1:91391371 | C | G | 1 | a0001c0004t0001g0156 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.494+2722G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391371 | |||||||
chr1:91391385 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.494+2708A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391385 | |||||||
chr1:91391548 | T | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(293): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.494+2545A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391548 | |||||||
chr1:91391812 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.494+2281G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391812 | |||||||
chr1:91391867 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.494+2226T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391867 | |||||||
chr1:91391949 | C | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.494+2144G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91391949 | |||||||
chr1:91392146 | G | A | 1 | a0001c0004t0001g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.494+1947C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392146 | |||||||
chr1:91392194 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+1899G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392194 | |||||||
chr1:91392553 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.494+1540T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392553 | |||||||
chr1:91392634 | T | C | 11 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.494+1459A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392634 | |||||||
chr1:91392650 | C | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
153 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.494+1443G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392650 | |||||||
chr1:91392783 | T | C | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.494+1310A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392783 | |||||||
chr1:91392784 | G | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(1): Show |
4 | HG01891.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+1309C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392784 | |||||||
chr1:91392833 | T | C | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.494+1260A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392833 | |||||||
chr1:91392929 | A | G | 2 | a0001c0001t0001g0308 a0001c0001t0001g0309 |
2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.494+1164T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91392929 | |||||||
chr1:91393090 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.494+1003A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393090 | |||||||
chr1:91393152 | T | C | 29 | a0002c0003t0001g0003 a0002c0003t0001g0178 a0002c0003t0001g0321 others(26): Show |
30 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.494+941A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393152 | |||||||
chr1:91393162 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.494+931G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393162 | |||||||
chr1:91393402 | A | G | 2 | a0001c0001t0001g0314 a0003c0012t0001g0142 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.494+691T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393402 | |||||||
chr1:91393547 | T | C | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.494+546A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393547 | |||||||
chr1:91393714 | T | C | 1 | a0001c0002t0001g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.494+379A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393714 | |||||||
chr1:91393738 | A | ACT | 6 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+354_494+355ins others(2): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393738 | |||||||
chr1:91393739 | A | T | 6 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+354T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393739 | |||||||
chr1:91393740 | G | T | 6 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(3): Show |
6 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+353C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393740 | |||||||
chr1:91393818 | T | C | 22 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0184 others(19): Show |
22 | HG00408.hp1 HG01928.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.494+275A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393818 | |||||||
chr1:91393964 | T | G | 2 | a0003c0009t0001g0197 a0003c0013t0001g0143 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.494+129A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393964 | |||||||
chr1:91393968 | G | A | 5 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+125C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91393968 | |||||||
chr1:91394011 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.494+82A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 4/38 | chr1 | 91394011 | |||||||
chr1:91394408 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.185-6T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394408 | |||||||
chr1:91394441 | A | C | 2 | a0001c0004t0001g0171 a0001c0004t0001g0172 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.185-39T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394441 | |||||||
chr1:91394579 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.185-177G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394579 | |||||||
chr1:91394671 | T | C | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.185-269A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394671 | |||||||
chr1:91394947 | G | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | NA18982.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.185-545C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394947 | |||||||
chr1:91394995 | A | T | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00408.hp2 HG00438.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-593T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91394995 | |||||||
chr1:91395023 | G | GTA | 11 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(8): Show |
11 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.185-623_185-622dup others(2): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395023 | |||||||
chr1:91395073 | G | A | 49 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(46): Show |
50 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.185-671C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395073 | |||||||
chr1:91395132 | C | G | 6 | a0001c0007t0001g0188 a0001c0007t0001g0190 a0001c0007t0001g0193 others(3): Show |
6 | HG00609.hp1 NA18943.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-730G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395132 | |||||||
chr1:91395206 | A | C | 355 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(352): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.185-804T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395206 | |||||||
chr1:91395392 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 |
3 | HG01891.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.184+901A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395392 | |||||||
chr1:91395719 | G | A | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.184+574C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395719 | |||||||
chr1:91395973 | C | T | 5 | a0001c0004t0001g0156 a0001c0004t0001g0157 a0001c0004t0001g0158 others(2): Show |
5 | HG01070.hp2 HG01123.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+320G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91395973 | |||||||
chr1:91396028 | T | C | 2 | a0002c0003t0001g0003 a0002c0003t0001g0178 |
3 | HG00280.hp1 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.184+265A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 3/38 | chr1 | 91396028 | |||||||
chr1:91396493 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.72-88G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396493 | |||||||
chr1:91396494 | T | C | 13 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-89A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396494 | |||||||
chr1:91396531 | T | C | 1 | a0007c0020t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72-126A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396531 | |||||||
chr1:91396643 | C | T | 48 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(45): Show |
49 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.72-238G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396643 | |||||||
chr1:91396650 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.72-245G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396650 | |||||||
chr1:91396700 | C | T | 2 | a0001c0001t0001g0306 a0002c0003t0001g0344 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.72-295G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396700 | |||||||
chr1:91396735 | A | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-330T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396735 | |||||||
chr1:91396755 | T | C | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-350A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396755 | |||||||
chr1:91396770 | A | T | 13 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-365T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396770 | |||||||
chr1:91396952 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-547C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91396952 | |||||||
chr1:91397076 | G | A | 1 | a0002c0003t0001g0343 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.72-671C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397076 | |||||||
chr1:91397187 | G | T | 58 | a0001c0001t0001g0185 a0001c0002t0001g0001 a0001c0002t0001g0005 others(55): Show |
59 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.72-782C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397187 | |||||||
chr1:91397519 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.72-1114C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397519 | |||||||
chr1:91397627 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-1222T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397627 | |||||||
chr1:91397657 | T | C | 1 | a0002c0003t0001g0348 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.72-1252A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397657 | |||||||
chr1:91397822 | G | A | 1 | a0001c0019t0001g0134 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.72-1417C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397822 | |||||||
chr1:91397828 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.72-1423G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397828 | |||||||
chr1:91397888 | A | T | 1 | a0002c0003t0001g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.72-1483T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91397888 | |||||||
chr1:91398680 | T | A | 1 | a0001c0001t0001g0307 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.72-2275A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91398680 | |||||||
chr1:91398689 | CT | C | 11 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(8): Show |
11 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.72-2285delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91398689 | |||||||
chr1:91399060 | C | T | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.71+1952G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399060 | |||||||
chr1:91399335 | CAGAT | C | 4 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
4 | HG01123.hp2 HG01257.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+1673_71+1676del others(4): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399335 | |||||||
chr1:91399362 | A | G | 1 | a0003c0012t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71+1650T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399362 | |||||||
chr1:91399372 | C | G | 355 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(352): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.71+1640G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399372 | |||||||
chr1:91399565 | C | T | 49 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(46): Show |
50 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.71+1447G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399565 | |||||||
chr1:91399638 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.71+1374G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399638 | |||||||
chr1:91399659 | C | CT | 3 | a0004c0008t0001g0318 a0004c0008t0001g0319 a0004c0011t0001g0152 |
3 | HG02965.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.71+1352dupA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399659 | |||||||
chr1:91399780 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71+1232G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399780 | |||||||
chr1:91399870 | A | C | 1 | a0001c0004t0001g0155 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.71+1142T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399870 | |||||||
chr1:91399913 | CAT | C | 12 | a0001c0001t0001g0314 a0001c0005t0002g0144 a0001c0005t0002g0145 others(9): Show |
12 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.71+1097_71+1098del others(2): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399913 | |||||||
chr1:91399979 | T | C | 179 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
180 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.71+1033A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399979 | |||||||
chr1:91399999 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.71+1013C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91399999 | |||||||
chr1:91400149 | A | C | 1 | a0003c0013t0001g0143 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71+863T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400149 | |||||||
chr1:91400156 | TAATAC | T | 2 | a0002c0003t0001g0003 a0002c0003t0001g0178 |
3 | HG00280.hp1 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.71+851_71+855delGT others(3): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400156 | |||||||
chr1:91400285 | C | T | 6 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.71+727G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400285 | |||||||
chr1:91400480 | CT | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(251): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.71+531delA | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400480 | |||||||
chr1:91400583 | G | A | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71+429C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400583 | |||||||
chr1:91400662 | T | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.71+350A>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400662 | |||||||
chr1:91400855 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.71+157T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400855 | |||||||
chr1:91400881 | G | C | 15 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0313 others(12): Show |
15 | HG01891.hp2 HG02083.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.71+131C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 2/38 | chr1 | 91400881 | |||||||
chr1:91401194 | C | G | 41 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(38): Show |
42 | HG00323.hp2 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.-27-85G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401194 | |||||||
chr1:91401299 | C | G | 22 | a0001c0004t0001g0155 a0001c0004t0001g0156 a0001c0004t0001g0157 others(19): Show |
22 | HG01070.hp2 HG01074.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-27-190G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401299 | |||||||
chr1:91401489 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-27-380A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401489 | |||||||
chr1:91401527 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-27-418G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401527 | |||||||
chr1:91401777 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-668G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401777 | |||||||
chr1:91401866 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-27-757G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401866 | |||||||
chr1:91401896 | G | A | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-787C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401896 | |||||||
chr1:91401917 | T | TA | 79 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(76): Show |
80 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27-809dupT | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401917 | |||||||
chr1:91401918 | A | T | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0003c0012t0001g0142 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-809T>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91401918 | |||||||
chr1:91402011 | T | C | 1 | a0001c0002t0001g0055 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-27-902A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91402011 | |||||||
chr1:91402121 | T | A | 1 | a0001c0001t0001g0358 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-27-1012A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91402121 | |||||||
chr1:91402217 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-27-1108C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91402217 | |||||||
chr1:91402824 | A | G | 1 | a0001c0001t0004g0012 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-27-1715T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91402824 | |||||||
chr1:91402865 | T | C | 1 | a0001c0001t0001g0349 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-27-1756A>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91402865 | |||||||
chr1:91403250 | A | G | 8 | a0001c0005t0002g0144 a0001c0005t0002g0145 a0001c0005t0002g0146 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+1548T>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91403250 | |||||||
chr1:91403329 | A | C | 2 | a0003c0012t0001g0142 a0003c0013t0001g0143 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-28+1469T>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91403329 | |||||||
chr1:91403674 | C | T | 1 | a0001c0016t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28+1124G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91403674 | |||||||
chr1:91403932 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(85): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-28+866G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91403932 | |||||||
chr1:91404193 | C | T | 6 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0008 others(3): Show |
6 | NA18944.hp2 NA18965.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+605G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404193 | |||||||
chr1:91404199 | C | A | 1 | a0001c0001t0001g0350 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-28+599G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404199 | |||||||
chr1:91404210 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | NA18970.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-28+588G>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404210 | |||||||
chr1:91404290 | C | A | 1 | a0001c0017t0001g0351 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-28+508G>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404290 | |||||||
chr1:91404325 | GTGGCACA others(12): Show |
G | 1 | a0001c0002t0001g0005 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-28+454_-28+472del others(19): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404325 | |||||||
chr1:91404428 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | NA18945.hp1 NA18959.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-28+370G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404428 | |||||||
chr1:91404433 | G | A | 50 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(47): Show |
51 | HG00323.hp2 HG00735.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.-28+365C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404433 | |||||||
chr1:91404532 | T | A | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-28+266A>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404532 | |||||||
chr1:91404573 | G | A | 306 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0056 others(303): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-28+225C>T | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404573 | |||||||
chr1:91404641 | G | C | 2 | a0001c0001t0001g0354 a0001c0001t0001g0355 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-28+157C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404641 | |||||||
chr1:91404669 | G | C | 1 | a0001c0002t0001g0005 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-28+129C>G | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404669 | |||||||
chr1:91404670 | C | G | 1 | a0001c0002t0001g0005 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-28+128G>C | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404670 | |||||||
chr1:91404732 | ACTTCCCC others(25): Show |
A | 3 | a0001c0001t0001g0356 a0001c0001t0001g0357 a0001c0001t0001g0358 |
3 | HG00639.hp1 HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-28+34_-28+65delGT others(30): Show |
HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404732 | |||||||
chr1:91404782 | G | T | 1 | a0001c0002t0001g0005 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-28+16C>A | HFM1 | ENSG00000162669.16 | transcript | ENST00000370425.8 | protein_coding | 1/38 | chr1 | 91404782 |