Item | Value |
---|---|
geneid | 79152 |
ensemblid | ENSG00000103089.9 |
hgncid | 21197 |
symbol | FA2H |
name | fatty acid 2-hydroxylase |
refseq_nuc | NM_024306.5 |
refseq_prot | NP_077282.3 |
ensembl_nuc | ENST00000219368.8 |
ensembl_prot | ENSP00000219368.3 |
mane_status | MANE Select |
chr | chr16 |
start | 74712969 |
end | 74774820 |
strand | - |
ver | v1.2 |
region | chr16:74712969-74774820 |
region5000 | chr16:74707969-74779820 |
regionname0 | FA2H_chr16_74712969_74774820 |
regionname5000 | FA2H_chr16_74707969_74779820 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 372 | 379 | 87 | 65 | 164 | 15 | 46 | 124 | FA2H_chr16_74707969_74779820 | FA2H | MAPAP others(367): Show |
chr16 | 74707969 | 74779820 |
a0002 | 0/0 | 372 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | MAPAP others(367): Show |
chr16 | 74707969 | 74779820 |
a0003 | 0/0 | 372 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | MAPAP others(367): Show |
chr16 | 74707969 | 74779820 |
a0004 | 0/0 | 372 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | MAPAP others(367): Show |
chr16 | 74707969 | 74779820 |
a0005 | 0/0 | 372 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | MAPAP others(367): Show |
chr16 | 74707969 | 74779820 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1116 | 203 | 27 | 39 | 99 | 8 | 29 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0002 | 1/0 | 1116 | 75 | 6 | 12 | 46 | 2 | 8 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0003 | 0/0 | 1116 | 44 | 26 | 5 | 4 | 4 | 5 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0004 | 0/0 | 1116 | 16 | 10 | 3 | 2 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0005 | 0/0 | 1116 | 14 | 9 | 0 | 5 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0006 | 0/0 | 1116 | 9 | 2 | 5 | 0 | 1 | 1 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0007 | 0/0 | 1116 | 6 | 0 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0008 | 0/0 | 1116 | 5 | 3 | 1 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0010 | 0/0 | 1116 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0012 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0013 | 0/0 | 1116 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0014 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0018 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0001c0019 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0002c0009 | 0/0 | 1116 | 3 | 3 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0002c0016 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0002c0017 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0002c0020 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0003c0011 | 0/0 | 1116 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0004c0015 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 | ||
a0005c0021 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | ATGGC others(1111): Show |
chr16 | 74707969 | 74779820 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2405 | 115 | 14 | 12 | 73 | 2 | 13 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0002 | 0/0 | 2405 | 42 | 3 | 19 | 15 | 0 | 5 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0003 | 0/0 | 2405 | 29 | 6 | 6 | 4 | 3 | 10 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0005 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0006 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0007 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0008 | 0/0 | 2405 | 3 | 0 | 0 | 3 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0011 | 0/0 | 2405 | 2 | 1 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0014 | 0/0 | 2405 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0018 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0022 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0023 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0024 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0026 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0028 | 0/0 | 2390 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2385): Show |
chr16 | 74707969 | 74779820 |
a0001c0001t0030 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0001 | 1/0 | 2405 | 63 | 1 | 12 | 42 | 1 | 6 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0002 | 0/0 | 2405 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0003 | 0/0 | 2405 | 5 | 4 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0006 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0008 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0015 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0002t0029 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0001 | 0/0 | 2405 | 13 | 5 | 1 | 4 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0002 | 0/0 | 2405 | 13 | 7 | 3 | 0 | 2 | 1 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0003 | 0/0 | 2405 | 9 | 5 | 1 | 0 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0005 | 0/0 | 2405 | 6 | 6 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0009 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0003t0011 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0001 | 0/0 | 2405 | 2 | 1 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0004 | 0/0 | 2405 | 8 | 6 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0006 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0007 | 0/0 | 2405 | 3 | 0 | 1 | 1 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0019 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0004t0025 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0004 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0006 | 0/0 | 2405 | 4 | 0 | 0 | 4 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0007 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0010 | 0/0 | 2405 | 4 | 4 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0012 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0005t0013 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0006t0001 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0006t0002 | 0/0 | 2405 | 8 | 2 | 4 | 0 | 1 | 1 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0007t0001 | 0/0 | 2405 | 6 | 0 | 0 | 6 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0008t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0008t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0008t0009 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0008t0027 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0010t0001 | 0/0 | 2405 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0012t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0013t0001 | 0/0 | 2405 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0014t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0018t0003 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0001c0019t0016 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0002c0009t0001 | 0/0 | 2405 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0002c0009t0012 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0002c0016t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0002c0017t0021 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0002c0020t0017 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0003c0011t0020 | 0/0 | 2405 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0004c0015t0001 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
a0005c0021t0001 | 0/0 | 2405 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | AGAGG others(2400): Show |
chr16 | 74707969 | 74779820 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0047 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0011g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0014g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0014g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0018g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0022g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0023g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0024g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0026g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0028g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0001t0030g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0015g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0002t0029g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0009g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0003t0011g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0019g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0004t0025g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0012g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0005t0013g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0006t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0007t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0009g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0009g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0008t0027g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0010t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0010t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0012t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0013t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0014t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0018t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0001c0019t0016g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0009t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0016t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0017t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0002c0020t0017g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0003c0011t0020g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0004c0015t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
a0005c0021t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0311 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0179 | EUR | GBR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00280 | hp2 | a0001 | c0001 | t0011 | g0239 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00323 | hp1 | a0001 | c0001 | t0030 | g0156 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00323 | hp2 | a0001 | c0006 | t0002 | g0331 | EUR | FIN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0285 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00621 | hp2 | a0001 | c0001 | t0026 | g0045 | EAS | CHS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00639 | hp1 | a0001 | c0006 | t0002 | g0330 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00735 | hp2 | a0001 | c0006 | t0002 | g0342 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01069 | hp1 | a0001 | c0004 | t0004 | g0015 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01069 | hp2 | a0001 | c0004 | t0007 | g0088 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01071 | hp1 | a0003 | c0011 | t0020 | g0019 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01071 | hp2 | a0001 | c0004 | t0004 | g0015 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01074 | hp2 | a0001 | c0006 | t0002 | g0334 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01192 | hp1 | a0001 | c0006 | t0001 | g0300 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01256 | hp2 | a0001 | c0008 | t0027 | g0340 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01257 | hp1 | a0001 | c0003 | t0002 | g0307 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01257 | hp2 | a0001 | c0003 | t0002 | g0338 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01258 | hp2 | a0001 | c0003 | t0002 | g0306 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01358 | hp1 | a0001 | c0003 | t0003 | g0017 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0212 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0201 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01516 | hp1 | a0004 | c0015 | t0001 | g0295 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0016 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01517 | hp1 | a0001 | c0003 | t0002 | g0016 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0215 | EUR | IBS | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01884 | hp2 | a0001 | c0019 | t0016 | g0359 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0348 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0085 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0301 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02040 | hp2 | a0001 | c0005 | t0007 | g0325 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02055 | hp2 | a0001 | c0004 | t0004 | g0274 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02071 | hp1 | a0001 | c0007 | t0001 | g0043 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0063 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02145 | hp1 | a0001 | c0008 | t0009 | g0365 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02145 | hp2 | a0001 | c0008 | t0003 | g0351 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02257 | hp1 | a0001 | c0005 | t0012 | g0360 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02257 | hp2 | a0001 | c0003 | t0003 | g0337 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02258 | hp1 | a0001 | c0002 | t0015 | g0193 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0314 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02293 | hp2 | a0001 | c0001 | t0014 | g0039 | AMR | PEL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02451 | hp1 | a0001 | c0003 | t0003 | g0317 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02451 | hp2 | a0001 | c0018 | t0003 | g0329 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02572 | hp1 | a0001 | c0008 | t0009 | g0366 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02572 | hp2 | a0001 | c0003 | t0009 | g0346 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02615 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02615 | hp2 | a0001 | c0003 | t0005 | g0298 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0014 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0322 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02647 | hp2 | a0001 | c0003 | t0005 | g0361 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0336 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0326 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0354 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02717 | hp2 | a0001 | c0004 | t0004 | g0275 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02738 | hp2 | a0001 | c0003 | t0003 | g0344 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02809 | hp1 | a0001 | c0005 | t0010 | g0318 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0327 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02818 | hp2 | a0001 | c0004 | t0004 | g0014 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02886 | hp1 | a0001 | c0012 | t0001 | g0020 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02886 | hp2 | a0001 | c0001 | t0024 | g0028 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02895 | hp2 | a0001 | c0006 | t0002 | g0333 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02896 | hp2 | a0002 | c0009 | t0001 | g0210 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02897 | hp1 | a0001 | c0006 | t0002 | g0332 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02897 | hp2 | a0002 | c0009 | t0001 | g0208 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0345 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02922 | hp2 | a0001 | c0003 | t0005 | g0362 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0130 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0364 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02970 | hp2 | a0002 | c0016 | t0001 | g0209 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02976 | hp1 | a0001 | c0003 | t0002 | g0349 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0128 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03041 | hp2 | a0002 | c0020 | t0017 | g0353 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0358 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0321 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03130 | hp2 | a0001 | c0001 | t0023 | g0291 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03225 | hp1 | a0001 | c0004 | t0004 | g0294 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0297 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03453 | hp1 | a0005 | c0021 | t0001 | g0367 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03453 | hp2 | a0001 | c0004 | t0004 | g0205 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03486 | hp2 | a0001 | c0003 | t0003 | g0355 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03490 | hp1 | a0001 | c0010 | t0001 | g0223 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03492 | hp2 | a0001 | c0010 | t0001 | g0243 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03516 | hp1 | a0001 | c0005 | t0010 | g0323 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0126 | AFR | ESN | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03579 | hp1 | a0001 | c0005 | t0013 | g0018 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03579 | hp2 | a0001 | c0003 | t0005 | g0363 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03654 | hp1 | a0001 | c0006 | t0002 | g0339 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03669 | hp2 | a0001 | c0004 | t0007 | g0106 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0328 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03710 | hp1 | a0001 | c0001 | t0018 | g0267 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0250 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | BEB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04199 | hp2 | a0001 | c0003 | t0003 | g0343 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0287 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0178 | SAS | STU | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18522 | hp2 | a0001 | c0005 | t0013 | g0018 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18612 | hp1 | a0001 | c0002 | t0008 | g0169 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0357 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0320 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18939 | hp2 | a0001 | c0002 | t0008 | g0110 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18946 | hp1 | a0001 | c0007 | t0001 | g0007 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18946 | hp2 | a0001 | c0001 | t0028 | g0053 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18947 | hp1 | a0001 | c0007 | t0001 | g0007 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18948 | hp1 | a0001 | c0005 | t0006 | g0305 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18959 | hp1 | a0001 | c0005 | t0006 | g0299 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18999 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA18999 | hp2 | a0001 | c0008 | t0001 | g0304 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19000 | hp1 | a0001 | c0005 | t0006 | g0302 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19003 | hp2 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19004 | hp2 | a0001 | c0007 | t0001 | g0042 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19007 | hp2 | a0001 | c0005 | t0006 | g0303 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19011 | hp2 | a0001 | c0013 | t0001 | g0111 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19030 | hp2 | a0001 | c0003 | t0011 | g0356 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0335 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19043 | hp2 | a0001 | c0004 | t0025 | g0206 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19054 | hp1 | a0001 | c0004 | t0007 | g0057 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19056 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19064 | hp2 | a0001 | c0002 | t0029 | g0195 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19074 | hp2 | a0001 | c0002 | t0006 | g0268 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19077 | hp1 | a0001 | c0007 | t0001 | g0144 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19079 | hp2 | a0001 | c0007 | t0001 | g0041 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19085 | hp2 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19240 | hp1 | a0001 | c0005 | t0010 | g0319 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ASW | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | ASW | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20752 | hp1 | a0001 | c0001 | t0022 | g0235 | EUR | TSI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20752 | hp2 | a0001 | c0003 | t0003 | g0017 | EUR | TSI | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | GIH | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | GIH | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG01123 | hp2 | a0001 | c0006 | t0002 | g0341 | AMR | CLM | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02109 | hp1 | a0001 | c0005 | t0010 | g0324 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02109 | hp2 | a0001 | c0014 | t0003 | g0132 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02486 | hp1 | a0001 | c0004 | t0019 | g0276 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02486 | hp2 | a0001 | c0005 | t0004 | g0316 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG02559 | hp2 | a0002 | c0017 | t0021 | g0027 | AFR | ACB | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03471 | hp1 | a0002 | c0009 | t0012 | g0094 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG03471 | hp2 | a0001 | c0003 | t0009 | g0347 | AFR | MSL | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0352 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0293 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0350 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
NA21309 | hp2 | a0001 | c0004 | t0006 | g0031 | AFR | LWK | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0047 | REF | REF | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0127 | REF | REF | FA2H_chr16_74707969_74779820 | FA2H | chr16 | 74707969 | 74779820 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74718989 | T | G | 1 | a0004 | 1 | HG01516.hp1 | missense_variant&splice_region_variant | MODERATE | c.785A>C | p.Lys262Thr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/7 | 850/2405 | 785/1119 | 262/372 | chr16 | 74718989 | |||
chr16:74740097 | G | C | 1 | a0002 | 6 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.289C>G | p.Pro97Ala | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/7 | 354/2405 | 289/1119 | 97/372 | chr16 | 74740097 | |||
chr16:74774625 | G | T | 1 | a0003 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.131C>A | p.Pro44Gln | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 196/2405 | 131/1119 | 44/372 | chr16 | 74774625 | |||
chr16:74774671 | G | C | 1 | a0005 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.85C>G | p.Arg29Gly | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 150/2405 | 85/1119 | 29/372 | chr16 | 74774671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74714196 | C | G | 2 | a0001c0014 a0001c0018 |
2 | HG02109.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.1113G>C | p.Thr371Thr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1178/2405 | 1113/1119 | 371/372 | chr16 | 74714196 | |||
chr16:74716417 | C | T | 1 | a0001c0013 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.969G>A | p.Pro323Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 1034/2405 | 969/1119 | 323/372 | chr16 | 74716417 | |||
chr16:74716453 | A | G | 3 | a0001c0004 a0001c0005 a0002c0009 |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
synonymous_variant | LOW | c.933T>C | p.Tyr311Tyr | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 998/2405 | 933/1119 | 311/372 | chr16 | 74716453 | |||
chr16:74716498 | T | C | 5 | a0001c0004 a0001c0005 a0001c0006 others(2): Show |
44 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
synonymous_variant | LOW | c.888A>G | p.Val296Val | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 953/2405 | 888/1119 | 296/372 | chr16 | 74716498 | |||
chr16:74716507 | G | A | 12 | a0001c0001 a0001c0003 a0001c0006 others(9): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
synonymous_variant | LOW | c.879C>T | p.Pro293Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/7 | 944/2405 | 879/1119 | 293/372 | chr16 | 74716507 | |||
chr16:74726301 | C | T | 1 | a0001c0007 | 6 | HG02071.hp1 NA18946.hp1 NA18947.hp1 others(3): Show |
synonymous_variant | LOW | c.537G>A | p.Leu179Leu | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/7 | 602/2405 | 537/1119 | 179/372 | chr16 | 74726301 | |||
chr16:74727306 | C | A | 1 | a0001c0019 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.444G>T | p.Pro148Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/7 | 509/2405 | 444/1119 | 148/372 | chr16 | 74727306 | |||
chr16:74774527 | G | A | 8 | a0001c0003 a0001c0005 a0001c0006 others(5): Show |
76 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(73): Show |
synonymous_variant | LOW | c.229C>T | p.Leu77Leu | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 294/2405 | 229/1119 | 77/372 | chr16 | 74774527 | |||
chr16:74774558 | C | G | 1 | a0001c0012 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.198G>C | p.Pro66Pro | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/7 | 263/2405 | 198/1119 | 66/372 | chr16 | 74774558 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74713059 | T | G | 10 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0024 others(7): Show |
18 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1131A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1131 | chr16 | 74713059 | ||||||
chr16:74713061 | C | T | 2 | a0001c0001t0024 a0001c0005t0010 |
5 | HG02109.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1129G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1129 | chr16 | 74713061 | ||||||
chr16:74713123 | C | T | 1 | a0001c0004t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1067 | chr16 | 74713123 | ||||||
chr16:74713126 | G | C | 22 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(19): Show |
75 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1064C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 1064 | chr16 | 74713126 | ||||||
chr16:74713232 | G | A | 1 | a0001c0005t0013 | 2 | HG03579.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*958C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 958 | chr16 | 74713232 | ||||||
chr16:74713353 | G | A | 1 | a0001c0001t0026 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*837C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 837 | chr16 | 74713353 | ||||||
chr16:74713369 | G | C | 1 | a0001c0008t0027 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*821C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 821 | chr16 | 74713369 | ||||||
chr16:74713369 | GGGGAGGT others(8): Show |
G | 1 | a0001c0001t0028 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806_*820delAGTGCC others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 806 | chr16 | 74713369 | ||||||
chr16:74713377 | G | A | 1 | a0001c0001t0014 | 2 | HG01975.hp1 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*813C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 813 | chr16 | 74713377 | ||||||
chr16:74713407 | C | T | 2 | a0001c0001t0008 a0001c0002t0008 |
5 | NA18612.hp1 NA18939.hp2 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*783G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 783 | chr16 | 74713407 | ||||||
chr16:74713553 | C | G | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0014 others(9): Show |
75 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*637G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 637 | chr16 | 74713553 | ||||||
chr16:74713594 | T | G | 1 | a0001c0002t0029 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*596A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 596 | chr16 | 74713594 | ||||||
chr16:74713650 | G | A | 1 | a0001c0001t0030 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 540 | chr16 | 74713650 | ||||||
chr16:74713670 | C | T | 1 | a0001c0001t0022 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*520G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 520 | chr16 | 74713670 | ||||||
chr16:74713786 | A | T | 16 | a0001c0001t0006 a0001c0001t0007 a0001c0002t0006 others(13): Show |
32 | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*404T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 404 | chr16 | 74713786 | ||||||
chr16:74713907 | C | G | 12 | a0001c0001t0005 a0001c0001t0018 a0001c0003t0005 others(9): Show |
27 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*283G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 283 | chr16 | 74713907 | ||||||
chr16:74713909 | G | T | 12 | a0001c0001t0005 a0001c0001t0018 a0001c0003t0005 others(9): Show |
27 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*281C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 281 | chr16 | 74713909 | ||||||
chr16:74713947 | C | T | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0003t0005 others(1): Show |
9 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*243G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 243 | chr16 | 74713947 | ||||||
chr16:74714156 | C | T | 2 | a0001c0002t0015 a0001c0019t0016 |
2 | HG01884.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*34G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 7/7 | 34 | chr16 | 74714156 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:74714447 | T | C | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1040-178A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714447 | |||||||
chr16:74714531 | C | T | 1 | a0001c0001t0011g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1040-262G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714531 | |||||||
chr16:74714725 | A | G | 17 | a0001c0004t0001g0063 a0001c0004t0007g0057 a0001c0004t0007g0088 others(14): Show |
17 | HG01069.hp2 HG01884.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1040-456T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714725 | |||||||
chr16:74714825 | G | C | 3 | a0001c0005t0012g0360 a0001c0005t0013g0018 a0002c0009t0012g0094 |
4 | HG02257.hp1 HG03471.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-556C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714825 | |||||||
chr16:74714834 | AT | A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0255 a0001c0001t0001g0281 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.1040-566delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | |||||||
chr16:74714834 | ATT | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
94 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1040-567_1040-566d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | |||||||
chr16:74714834 | ATTT | A | 20 | a0001c0001t0001g0078 a0001c0001t0001g0151 a0001c0004t0001g0063 others(17): Show |
20 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1040-568_1040-566d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714834 | |||||||
chr16:74714871 | T | C | 4 | a0001c0005t0006g0299 a0001c0005t0006g0302 a0001c0005t0006g0303 others(1): Show |
4 | NA18948.hp1 NA18959.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-602A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714871 | |||||||
chr16:74714983 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
108 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1040-714G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74714983 | |||||||
chr16:74715024 | GA | G | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040-756delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715024 | |||||||
chr16:74715239 | T | A | 1 | a0001c0003t0003g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1040-970A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715239 | |||||||
chr16:74715362 | GC | G | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+984delG | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715362 | |||||||
chr16:74715492 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1039+855A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715492 | |||||||
chr16:74715545 | G | A | 14 | a0001c0004t0001g0293 a0001c0004t0004g0014 a0001c0004t0004g0015 others(11): Show |
17 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039+802C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715545 | |||||||
chr16:74715687 | G | A | 1 | a0001c0005t0010g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1039+660C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715687 | |||||||
chr16:74715768 | C | G | 6 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0001t0002g0256 others(3): Show |
6 | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039+579G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715768 | |||||||
chr16:74715790 | C | T | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+557G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715790 | |||||||
chr16:74715794 | C | T | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+553G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715794 | |||||||
chr16:74715799 | C | T | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+548G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715799 | |||||||
chr16:74715800 | T | TTTC | 11 | a0001c0004t0001g0063 a0001c0004t0007g0106 a0001c0005t0006g0299 others(8): Show |
11 | HG02040.hp2 HG02109.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039+544_1039+546d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715800 | |||||||
chr16:74715812 | C | CTTTTTTT others(16): Show |
3 | a0001c0004t0001g0293 a0002c0009t0001g0208 a0002c0009t0001g0210 |
3 | HG02896.hp2 HG02897.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1039+534_1039+535i others(25): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715812 | |||||||
chr16:74715815 | C | T | 14 | a0001c0004t0001g0293 a0001c0004t0004g0014 a0001c0004t0004g0015 others(11): Show |
16 | HG01071.hp2 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1039+532G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715815 | |||||||
chr16:74715815 | CT | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0277 others(8): Show |
11 | HG00738.hp1 HG01981.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.1039+531delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715815 | |||||||
chr16:74715818 | T | C | 2 | a0001c0002t0001g0145 a0001c0002t0001g0147 |
2 | NA19011.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1039+529A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715818 | |||||||
chr16:74715832 | T | A | 35 | a0001c0001t0005g0183 a0001c0003t0003g0322 a0001c0003t0005g0298 others(32): Show |
38 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1039+515A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715832 | |||||||
chr16:74715854 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
118 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1039+493A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715854 | |||||||
chr16:74715855 | G | A | 44 | a0001c0001t0005g0183 a0001c0003t0003g0322 a0001c0003t0005g0298 others(41): Show |
47 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1039+492C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715855 | |||||||
chr16:74715876 | T | C | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+471A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715876 | |||||||
chr16:74715958 | G | A | 1 | a0001c0002t0029g0195 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1039+389C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74715958 | |||||||
chr16:74716004 | C | T | 26 | a0001c0004t0001g0063 a0001c0004t0004g0014 a0001c0004t0004g0015 others(23): Show |
29 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1039+343G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716004 | |||||||
chr16:74716105 | C | T | 13 | a0001c0004t0001g0063 a0001c0004t0007g0057 a0001c0004t0007g0088 others(10): Show |
13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039+242G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716105 | |||||||
chr16:74716209 | G | A | 1 | a0001c0004t0007g0057 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1039+138C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716209 | |||||||
chr16:74716219 | T | C | 2 | a0001c0002t0001g0113 a0001c0002t0001g0207 |
2 | HG02080.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1039+128A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716219 | |||||||
chr16:74716236 | A | G | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1039+111T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716236 | |||||||
chr16:74716244 | C | A | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+103G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716244 | |||||||
chr16:74716245 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1039+102C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716245 | |||||||
chr16:74716285 | G | A | 1 | a0001c0006t0002g0339 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1039+62C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716285 | |||||||
chr16:74716331 | A | C | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1039+16T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716331 | |||||||
chr16:74716339 | A | G | 40 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 others(37): Show |
43 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.1039+8T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 6/6 | chr16 | 74716339 | |||||||
chr16:74716658 | A | G | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-59T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716658 | |||||||
chr16:74716695 | G | A | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-96C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716695 | |||||||
chr16:74716748 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.787-149C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716748 | |||||||
chr16:74716757 | C | T | 5 | a0001c0004t0025g0206 a0001c0005t0001g0358 a0001c0005t0012g0360 others(2): Show |
6 | HG02257.hp1 HG03098.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-158G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716757 | |||||||
chr16:74716788 | T | C | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-189A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716788 | |||||||
chr16:74716832 | C | T | 2 | a0001c0005t0001g0358 a0001c0005t0013g0018 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.787-233G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716832 | |||||||
chr16:74716976 | A | G | 13 | a0001c0004t0001g0063 a0001c0004t0007g0057 a0001c0004t0007g0088 others(10): Show |
13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-377T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74716976 | |||||||
chr16:74717048 | A | G | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-449T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717048 | |||||||
chr16:74717049 | A | G | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-450T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717049 | |||||||
chr16:74717074 | C | G | 12 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(9): Show |
15 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.787-475G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717074 | |||||||
chr16:74717084 | C | T | 4 | a0001c0001t0001g0067 a0001c0004t0001g0293 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-485G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717084 | |||||||
chr16:74717269 | G | A | 1 | a0001c0007t0001g0041 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.787-670C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717269 | |||||||
chr16:74717328 | A | G | 30 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(27): Show |
33 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-729T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717328 | |||||||
chr16:74717334 | T | G | 12 | a0001c0001t0003g0129 a0001c0006t0001g0300 a0001c0006t0002g0330 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-735A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717334 | |||||||
chr16:74717375 | G | C | 4 | a0001c0001t0003g0248 a0001c0001t0003g0249 a0001c0001t0003g0250 others(1): Show |
4 | HG03710.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-776C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717375 | |||||||
chr16:74717383 | A | G | 42 | a0001c0001t0003g0129 a0001c0004t0001g0063 a0001c0004t0001g0293 others(39): Show |
45 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.787-784T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717383 | |||||||
chr16:74717496 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.787-897G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717496 | |||||||
chr16:74717505 | G | A | 29 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(26): Show |
31 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.787-906C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717505 | |||||||
chr16:74717530 | G | A | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.787-931C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717530 | |||||||
chr16:74717532 | T | C | 41 | a0001c0004t0001g0063 a0001c0004t0001g0293 a0001c0004t0004g0014 others(38): Show |
44 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.787-933A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717532 | |||||||
chr16:74717634 | A | T | 26 | a0001c0004t0001g0063 a0001c0004t0004g0014 a0001c0004t0004g0015 others(23): Show |
29 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.787-1035T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717634 | |||||||
chr16:74717680 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.787-1081G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717680 | |||||||
chr16:74717722 | G | C | 1 | a0001c0002t0001g0125 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.787-1123C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717722 | |||||||
chr16:74717830 | G | A | 14 | a0001c0001t0005g0183 a0001c0003t0003g0322 a0001c0003t0005g0298 others(11): Show |
14 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+1158C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717830 | |||||||
chr16:74717929 | G | C | 13 | a0001c0004t0001g0063 a0001c0004t0007g0057 a0001c0004t0007g0088 others(10): Show |
13 | HG01069.hp2 HG02040.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+1059C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74717929 | |||||||
chr16:74718027 | C | G | 1 | a0001c0002t0001g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.786+961G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718027 | |||||||
chr16:74718028 | C | G | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.786+960G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718028 | |||||||
chr16:74718203 | C | T | 1 | a0001c0005t0010g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.786+785G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718203 | |||||||
chr16:74718244 | A | G | 10 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.786+744T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718244 | |||||||
chr16:74718261 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.786+727T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718261 | |||||||
chr16:74718273 | A | G | 15 | a0001c0001t0003g0129 a0001c0001t0005g0183 a0001c0003t0003g0322 others(12): Show |
15 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+715T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718273 | |||||||
chr16:74718278 | T | C | 24 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(21): Show |
27 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+710A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718278 | |||||||
chr16:74718298 | G | T | 1 | a0001c0003t0003g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.786+690C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718298 | |||||||
chr16:74718312 | G | C | 12 | a0001c0001t0003g0129 a0001c0006t0001g0300 a0001c0006t0002g0330 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+676C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718312 | |||||||
chr16:74718327 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.786+661A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718327 | |||||||
chr16:74718418 | G | A | 1 | a0001c0003t0005g0362 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.786+570C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718418 | |||||||
chr16:74718594 | T | G | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+394A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718594 | |||||||
chr16:74718624 | C | G | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+364G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718624 | |||||||
chr16:74718625 | G | A | 1 | a0001c0001t0018g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+363C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718625 | |||||||
chr16:74718637 | G | C | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.786+351C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718637 | |||||||
chr16:74718672 | G | A | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.786+316C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718672 | |||||||
chr16:74718706 | T | C | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.786+282A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718706 | |||||||
chr16:74718707 | G | C | 1 | a0002c0017t0021g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.786+281C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718707 | |||||||
chr16:74718750 | C | T | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.786+238G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718750 | |||||||
chr16:74718846 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.786+142G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718846 | |||||||
chr16:74718923 | G | C | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+65C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718923 | |||||||
chr16:74718943 | C | G | 38 | a0001c0001t0001g0089 a0001c0002t0015g0193 a0001c0004t0004g0014 others(35): Show |
41 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.786+45G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 5/6 | chr16 | 74718943 | |||||||
chr16:74719167 | G | C | 1 | a0001c0001t0003g0129 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.614-7C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719167 | |||||||
chr16:74719181 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.614-21G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719181 | |||||||
chr16:74719217 | C | T | 2 | a0001c0002t0015g0193 a0001c0019t0016g0359 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.614-57G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719217 | |||||||
chr16:74719224 | C | T | 4 | a0001c0004t0001g0293 a0001c0004t0006g0031 a0002c0009t0001g0208 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-64G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719224 | |||||||
chr16:74719249 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.614-89G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719249 | |||||||
chr16:74719570 | G | A | 5 | a0001c0002t0001g0177 a0001c0002t0001g0180 a0001c0002t0001g0181 others(2): Show |
5 | HG01361.hp1 HG01496.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.614-410C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719570 | |||||||
chr16:74719592 | C | T | 14 | a0001c0001t0005g0183 a0001c0003t0003g0322 a0001c0003t0005g0298 others(11): Show |
14 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.614-432G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719592 | |||||||
chr16:74719802 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.614-642G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74719802 | |||||||
chr16:74720082 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.614-922G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720082 | |||||||
chr16:74720125 | A | G | 12 | a0001c0004t0001g0293 a0001c0004t0004g0014 a0001c0004t0004g0015 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-965T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720125 | |||||||
chr16:74720139 | T | A | 1 | a0002c0017t0021g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.614-979A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720139 | |||||||
chr16:74720145 | C | G | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-985G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720145 | |||||||
chr16:74720162 | CAT | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.614-1004_614-1003d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720162 | |||||||
chr16:74720165 | A | AT | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-1006dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720165 | |||||||
chr16:74720167 | A | C | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-1007T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720167 | |||||||
chr16:74720180 | C | CT | 36 | a0001c0002t0001g0055 a0001c0002t0001g0095 a0001c0002t0001g0101 others(33): Show |
36 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.614-1021dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | C | CTT | 12 | a0001c0002t0001g0100 a0001c0002t0001g0162 a0001c0003t0001g0311 others(9): Show |
14 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.614-1022_614-1021d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | C | CTTT | 6 | a0001c0002t0001g0021 a0001c0003t0003g0322 a0001c0003t0005g0354 others(3): Show |
6 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1023_614-1021d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | C | CTTTT | 7 | a0001c0001t0005g0183 a0001c0002t0003g0130 a0001c0002t0003g0297 others(4): Show |
7 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1024_614-1021d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | C | CTTTTT | 6 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-1025_614-1021d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | C | CTTTTTTT others(3): Show |
1 | a0001c0006t0002g0342 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.614-1030_614-1021d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | CT | C | 75 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0046 others(72): Show |
77 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.614-1021delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | CTT | C | 84 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0038 others(81): Show |
90 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.614-1022_614-1021d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | CTTT | C | 13 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0083 others(10): Show |
13 | HG00408.hp2 HG00621.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.614-1023_614-1021d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | CTTTT | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.614-1024_614-1021d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720180 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.614-1030_614-1021d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720180 | |||||||
chr16:74720357 | G | C | 2 | a0001c0001t0001g0234 a0001c0001t0003g0227 |
2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.614-1197C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720357 | |||||||
chr16:74720384 | G | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.614-1224C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720384 | |||||||
chr16:74720442 | C | T | 1 | a0001c0003t0003g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.614-1282G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720442 | |||||||
chr16:74720583 | C | T | 2 | a0001c0003t0002g0345 a0001c0012t0001g0020 |
2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.614-1423G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720583 | |||||||
chr16:74720623 | A | T | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-1463T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720623 | |||||||
chr16:74720664 | C | T | 2 | a0001c0003t0001g0314 a0001c0003t0001g0352 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.614-1504G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720664 | |||||||
chr16:74720678 | T | G | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-1518A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720678 | |||||||
chr16:74720680 | A | G | 1 | a0001c0002t0001g0121 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.614-1520T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720680 | |||||||
chr16:74720720 | T | C | 4 | a0001c0003t0009g0346 a0001c0003t0009g0347 a0001c0008t0009g0365 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-1560A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74720720 | |||||||
chr16:74721198 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.614-2038C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721198 | |||||||
chr16:74721231 | G | A | 2 | a0001c0005t0001g0358 a0001c0005t0013g0018 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.614-2071C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721231 | |||||||
chr16:74721281 | C | T | 3 | a0001c0003t0002g0348 a0001c0003t0002g0349 a0001c0003t0002g0350 |
3 | HG01891.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.614-2121G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721281 | |||||||
chr16:74721365 | A | C | 1 | a0001c0013t0001g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.614-2205T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721365 | |||||||
chr16:74721447 | A | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.614-2287T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721447 | |||||||
chr16:74721554 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.614-2394C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721554 | |||||||
chr16:74721613 | T | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0032 others(183): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.614-2453A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721613 | |||||||
chr16:74721686 | T | G | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-2526A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721686 | |||||||
chr16:74721732 | C | G | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.614-2572G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721732 | |||||||
chr16:74721887 | G | A | 12 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.614-2727C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721887 | |||||||
chr16:74721906 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0240 a0001c0001t0011g0239 |
4 | HG00280.hp2 HG01255.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.614-2746T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74721906 | |||||||
chr16:74722032 | G | A | 24 | a0001c0001t0003g0129 a0001c0004t0001g0293 a0001c0004t0004g0014 others(21): Show |
26 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.614-2872C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722032 | |||||||
chr16:74722065 | A | T | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.614-2905T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722065 | |||||||
chr16:74722068 | C | A | 1 | a0001c0002t0001g0178 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.614-2908G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722068 | |||||||
chr16:74722189 | T | C | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.614-3029A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722189 | |||||||
chr16:74722220 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.614-3060G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722220 | |||||||
chr16:74722554 | G | A | 47 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 others(44): Show |
51 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.614-3394C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722554 | |||||||
chr16:74722825 | C | T | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.613+3400G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722825 | |||||||
chr16:74722911 | C | CA | 15 | a0001c0001t0001g0280 a0001c0002t0001g0114 a0001c0002t0001g0136 others(12): Show |
15 | HG01884.hp2 HG01952.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.613+3313dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | |||||||
chr16:74722911 | CA | C | 13 | a0001c0001t0005g0183 a0001c0002t0001g0059 a0001c0003t0005g0354 others(10): Show |
16 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.613+3313delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | |||||||
chr16:74722911 | CAA | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0261 a0001c0001t0002g0098 others(3): Show |
6 | HG01243.hp2 HG01978.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3312_613+3313d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | |||||||
chr16:74722911 | CAAA | C | 159 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(156): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.613+3311_613+3313d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | |||||||
chr16:74722911 | CAAAA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
76 | HG00280.hp1 HG00408.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.613+3310_613+3313d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74722911 | |||||||
chr16:74723027 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.613+3198G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723027 | |||||||
chr16:74723085 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.613+3140C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723085 | |||||||
chr16:74723111 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0279 a0001c0001t0001g0282 others(3): Show |
6 | HG00408.hp1 HG00438.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.613+3114C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723111 | |||||||
chr16:74723227 | C | T | 2 | a0001c0005t0001g0358 a0001c0005t0013g0018 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.613+2998G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723227 | |||||||
chr16:74723349 | G | A | 2 | a0001c0005t0001g0358 a0001c0005t0013g0018 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.613+2876C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723349 | |||||||
chr16:74723369 | T | C | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.613+2856A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723369 | |||||||
chr16:74723407 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0099 a0001c0001t0001g0228 others(2): Show |
5 | NA18943.hp2 NA18950.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+2818G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723407 | |||||||
chr16:74723412 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613+2813C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723412 | |||||||
chr16:74723420 | A | C | 1 | a0001c0001t0002g0048 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.613+2805T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723420 | |||||||
chr16:74723688 | C | A | 4 | a0001c0002t0015g0193 a0001c0005t0001g0358 a0001c0005t0013g0018 others(1): Show |
5 | HG01884.hp2 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.613+2537G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723688 | |||||||
chr16:74723732 | G | C | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.613+2493C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723732 | |||||||
chr16:74723820 | G | A | 172 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(169): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.613+2405C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74723820 | |||||||
chr16:74724233 | A | G | 1 | a0001c0003t0005g0362 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.613+1992T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724233 | |||||||
chr16:74724251 | C | T | 1 | a0001c0001t0008g0124 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.613+1974G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724251 | |||||||
chr16:74724404 | C | T | 1 | a0001c0002t0003g0201 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.613+1821G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724404 | |||||||
chr16:74724435 | T | C | 1 | a0001c0001t0001g0008 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.613+1790A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724435 | |||||||
chr16:74724465 | G | A | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+1760C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724465 | |||||||
chr16:74724571 | T | G | 1 | a0001c0003t0001g0308 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.613+1654A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724571 | |||||||
chr16:74724603 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.613+1622G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724603 | |||||||
chr16:74724740 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.613+1485A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724740 | |||||||
chr16:74724755 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.613+1470T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724755 | |||||||
chr16:74724797 | C | G | 1 | a0001c0003t0005g0362 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.613+1428G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724797 | |||||||
chr16:74724809 | A | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.613+1416T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724809 | |||||||
chr16:74724912 | C | T | 1 | a0002c0009t0012g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.613+1313G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724912 | |||||||
chr16:74724916 | G | A | 2 | a0001c0005t0012g0360 a0002c0009t0012g0094 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.613+1309C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74724916 | |||||||
chr16:74725013 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0081 |
2 | NA18942.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.613+1212G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725013 | |||||||
chr16:74725086 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.613+1139T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725086 | |||||||
chr16:74725233 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.613+992C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725233 | |||||||
chr16:74725243 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.613+982G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725243 | |||||||
chr16:74725318 | C | T | 4 | a0001c0002t0015g0193 a0001c0005t0013g0018 a0001c0008t0003g0351 others(1): Show |
5 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+907G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725318 | |||||||
chr16:74725350 | A | G | 1 | a0001c0001t0002g0262 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.613+875T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725350 | |||||||
chr16:74725421 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
67 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.613+804C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725421 | |||||||
chr16:74725492 | C | T | 32 | a0001c0003t0002g0016 a0001c0004t0004g0014 a0001c0004t0004g0015 others(29): Show |
35 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.613+733G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725492 | |||||||
chr16:74725531 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
66 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.613+694G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725531 | |||||||
chr16:74725532 | G | A | 1 | a0001c0003t0001g0312 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.613+693C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725532 | |||||||
chr16:74725608 | C | T | 5 | a0001c0002t0015g0193 a0001c0005t0001g0358 a0001c0005t0013g0018 others(2): Show |
6 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+617G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725608 | |||||||
chr16:74725656 | G | A | 1 | a0001c0004t0004g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.613+569C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725656 | |||||||
chr16:74725682 | C | T | 1 | a0001c0003t0003g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.613+543G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725682 | |||||||
chr16:74725691 | G | A | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.613+534C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725691 | |||||||
chr16:74725752 | C | T | 11 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.613+473G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725752 | |||||||
chr16:74725926 | G | A | 1 | a0001c0003t0001g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.613+299C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 4/6 | chr16 | 74725926 | |||||||
chr16:74726363 | C | A | 1 | a0001c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.507-32G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726363 | |||||||
chr16:74726394 | CT | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(294): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.507-64delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726394 | |||||||
chr16:74726423 | T | C | 12 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.507-92A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726423 | |||||||
chr16:74726523 | G | C | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.507-192C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726523 | |||||||
chr16:74726687 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(61): Show |
70 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.507-356C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726687 | |||||||
chr16:74726968 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.506+276C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726968 | |||||||
chr16:74726969 | C | A | 14 | a0001c0001t0001g0089 a0001c0001t0002g0290 a0001c0003t0001g0313 others(11): Show |
14 | HG01891.hp1 HG02280.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+275G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726969 | |||||||
chr16:74726970 | G | A | 1 | a0001c0005t0007g0325 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506+274C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726970 | |||||||
chr16:74726998 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.506+246T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 3/6 | chr16 | 74726998 | |||||||
chr16:74727424 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.364-38G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727424 | |||||||
chr16:74727587 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-201C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727587 | |||||||
chr16:74727595 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.364-209A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727595 | |||||||
chr16:74727626 | G | A | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-240C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727626 | |||||||
chr16:74727755 | G | A | 5 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(2): Show |
5 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-369C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727755 | |||||||
chr16:74727797 | TAAAGTCT others(20): Show |
T | 1 | a0001c0002t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.364-438_364-412del others(27): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727797 | |||||||
chr16:74727935 | T | A | 1 | a0001c0002t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.364-549A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727935 | |||||||
chr16:74727945 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(40): Show |
46 | HG00621.hp1 HG01975.hp1 HG02040.hp1 others(43): Show |
intron_variant | MODIFIER | c.364-559T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74727945 | |||||||
chr16:74728006 | C | A | 1 | a0001c0001t0002g0273 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.364-620G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728006 | |||||||
chr16:74728087 | A | G | 1 | a0001c0001t0028g0053 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.364-701T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728087 | |||||||
chr16:74728239 | T | C | 12 | a0001c0006t0001g0300 a0001c0006t0002g0330 a0001c0006t0002g0331 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-853A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728239 | |||||||
chr16:74728250 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.364-864A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728250 | |||||||
chr16:74728266 | T | C | 5 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(2): Show |
5 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-880A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728266 | |||||||
chr16:74728266 | T | G | 1 | a0001c0002t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.364-880A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728266 | |||||||
chr16:74728570 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.364-1184T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728570 | |||||||
chr16:74728722 | C | A | 1 | a0001c0001t0001g0008 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.364-1336G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728722 | |||||||
chr16:74728758 | T | C | 1 | a0001c0002t0001g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.364-1372A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728758 | |||||||
chr16:74728780 | C | CT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0150 a0001c0001t0001g0203 others(8): Show |
11 | HG02280.hp1 HG02559.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.364-1395dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | |||||||
chr16:74728780 | CT | C | 47 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0077 others(44): Show |
48 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.364-1395delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | |||||||
chr16:74728780 | CTT | C | 33 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(30): Show |
35 | HG00099.hp2 HG00323.hp2 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.364-1396_364-1395d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728780 | |||||||
chr16:74728784 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.364-1398A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728784 | |||||||
chr16:74728932 | A | T | 1 | a0001c0002t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.364-1546T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74728932 | |||||||
chr16:74729004 | A | AT | 73 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0080 others(70): Show |
78 | HG00099.hp2 HG00323.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.364-1619dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | |||||||
chr16:74729004 | A | ATT | 16 | a0001c0001t0002g0231 a0001c0001t0002g0236 a0001c0003t0002g0327 others(13): Show |
16 | HG00639.hp1 HG00735.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-1620_364-1619d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | |||||||
chr16:74729004 | A | ATTT | 8 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(5): Show |
8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.364-1621_364-1619d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | |||||||
chr16:74729004 | AT | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0067 a0001c0001t0001g0099 others(5): Show |
8 | HG01167.hp1 HG01975.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-1619delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729004 | |||||||
chr16:74729005 | T | A | 4 | a0001c0001t0001g0255 a0001c0001t0003g0173 a0001c0001t0003g0224 others(1): Show |
4 | HG01074.hp1 HG01167.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1619A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729005 | |||||||
chr16:74729060 | G | C | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1674C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729060 | |||||||
chr16:74729074 | G | C | 1 | a0001c0004t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.364-1688C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729074 | |||||||
chr16:74729171 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(60): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.364-1785G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729171 | |||||||
chr16:74729221 | G | A | 1 | a0001c0003t0003g0355 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.364-1835C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729221 | |||||||
chr16:74729277 | G | A | 22 | a0001c0003t0001g0311 a0001c0003t0002g0016 a0001c0004t0004g0014 others(19): Show |
25 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.364-1891C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729277 | |||||||
chr16:74729305 | G | A | 1 | a0001c0002t0002g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.364-1919C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729305 | |||||||
chr16:74729670 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.364-2284C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729670 | |||||||
chr16:74729846 | G | C | 1 | a0001c0003t0002g0016 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.364-2460C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729846 | |||||||
chr16:74729854 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.364-2468C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729854 | |||||||
chr16:74729967 | G | C | 15 | a0001c0001t0005g0183 a0001c0003t0003g0322 a0001c0003t0005g0298 others(12): Show |
15 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-2581C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729967 | |||||||
chr16:74729986 | A | C | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-2600T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74729986 | |||||||
chr16:74730142 | C | T | 1 | a0001c0003t0002g0327 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.364-2756G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730142 | |||||||
chr16:74730198 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.364-2812G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730198 | |||||||
chr16:74730233 | A | T | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.364-2847T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730233 | |||||||
chr16:74730535 | G | C | 4 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 others(1): Show |
4 | HG02965.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-3149C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730535 | |||||||
chr16:74730542 | A | AAC | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
97 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.364-3158_364-3157d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730542 | |||||||
chr16:74730679 | T | G | 15 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 others(12): Show |
15 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-3293A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730679 | |||||||
chr16:74730895 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
86 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.364-3509G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730895 | |||||||
chr16:74730932 | C | T | 4 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-3546G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730932 | |||||||
chr16:74730991 | G | A | 27 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0001g0352 others(24): Show |
30 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.364-3605C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74730991 | |||||||
chr16:74731156 | A | AT | 17 | a0001c0001t0001g0049 a0001c0001t0001g0080 a0001c0001t0001g0131 others(14): Show |
17 | HG01081.hp2 HG01515.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.364-3771dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731156 | |||||||
chr16:74731243 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.364-3857G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731243 | |||||||
chr16:74731257 | C | CCTGAGTA others(1): Show |
76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
82 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.364-3879_364-3872d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731257 | |||||||
chr16:74731298 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.364-3913dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731298 | |||||||
chr16:74731298 | CT | C | 20 | a0001c0002t0001g0136 a0001c0002t0001g0178 a0001c0002t0003g0126 others(17): Show |
21 | HG01256.hp2 HG01884.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-3913delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731298 | |||||||
chr16:74731391 | G | A | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.364-4005C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731391 | |||||||
chr16:74731456 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.364-4070G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731456 | |||||||
chr16:74731498 | G | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0266 |
2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.364-4112C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731498 | |||||||
chr16:74731595 | G | A | 169 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(166): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.364-4209C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731595 | |||||||
chr16:74731715 | C | T | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364-4329G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731715 | |||||||
chr16:74731765 | C | T | 1 | a0001c0013t0001g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.364-4379G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731765 | |||||||
chr16:74731925 | T | C | 3 | a0001c0003t0003g0322 a0001c0003t0005g0298 a0001c0003t0005g0354 |
3 | HG02615.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.364-4539A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74731925 | |||||||
chr16:74732206 | C | A | 14 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(11): Show |
15 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.364-4820G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732206 | |||||||
chr16:74732279 | G | A | 31 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0001g0352 others(28): Show |
34 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.364-4893C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732279 | |||||||
chr16:74732444 | CTTTTT | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0049 a0001c0001t0001g0064 others(7): Show |
11 | HG02165.hp1 NA18940.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-5063_364-5059d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732444 | |||||||
chr16:74732450 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.364-5064A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732450 | |||||||
chr16:74732451 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.364-5065A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732451 | |||||||
chr16:74732549 | G | C | 4 | a0001c0003t0009g0346 a0001c0003t0009g0347 a0001c0008t0009g0365 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-5163C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732549 | |||||||
chr16:74732669 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.364-5283G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74732669 | |||||||
chr16:74733155 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.364-5769C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733155 | |||||||
chr16:74733170 | T | C | 1 | a0001c0001t0018g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.364-5784A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733170 | |||||||
chr16:74733234 | G | A | 1 | a0001c0014t0003g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.364-5848C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733234 | |||||||
chr16:74733352 | C | T | 1 | a0001c0003t0003g0344 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.364-5966G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733352 | |||||||
chr16:74733630 | G | C | 1 | a0001c0007t0001g0042 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.364-6244C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733630 | |||||||
chr16:74733644 | A | T | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.364-6258T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733644 | |||||||
chr16:74733658 | G | A | 2 | a0001c0001t0003g0248 a0001c0006t0002g0341 |
2 | HG01123.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.364-6272C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733658 | |||||||
chr16:74733824 | C | T | 1 | a0001c0004t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.363+6199G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733824 | |||||||
chr16:74733835 | T | A | 169 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0033 others(166): Show |
174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.363+6188A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733835 | |||||||
chr16:74733960 | G | A | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+6063C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74733960 | |||||||
chr16:74734025 | C | T | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5998G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734025 | |||||||
chr16:74734048 | C | T | 1 | a0001c0002t0001g0176 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.363+5975G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734048 | |||||||
chr16:74734072 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.363+5951G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734072 | |||||||
chr16:74734085 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
62 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.363+5938C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734085 | |||||||
chr16:74734096 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+5927T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734096 | |||||||
chr16:74734156 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363+5867C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734156 | |||||||
chr16:74734171 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.363+5852C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734171 | |||||||
chr16:74734238 | G | T | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5785C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734238 | |||||||
chr16:74734350 | C | T | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.363+5673G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734350 | |||||||
chr16:74734395 | G | A | 1 | a0001c0003t0001g0312 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.363+5628C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734395 | |||||||
chr16:74734423 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+5600C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734423 | |||||||
chr16:74734458 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0049 others(15): Show |
20 | HG02165.hp1 NA18940.hp1 NA18942.hp2 others(17): Show |
intron_variant | MODIFIER | c.363+5565C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734458 | |||||||
chr16:74734635 | G | A | 3 | a0001c0002t0001g0125 a0001c0002t0001g0136 a0001c0002t0001g0192 |
3 | HG00642.hp1 HG00733.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.363+5388C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734635 | |||||||
chr16:74734732 | T | A | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.363+5291A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734732 | |||||||
chr16:74734914 | G | T | 112 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0036 others(109): Show |
115 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.363+5109C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734914 | |||||||
chr16:74734972 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.363+5051C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734972 | |||||||
chr16:74734978 | G | A | 11 | a0001c0001t0001g0131 a0001c0001t0002g0159 a0001c0001t0005g0183 others(8): Show |
11 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.363+5045C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74734978 | |||||||
chr16:74735021 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.363+5002C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735021 | |||||||
chr16:74735186 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.363+4837C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735186 | |||||||
chr16:74735189 | G | T | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+4834C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735189 | |||||||
chr16:74735333 | G | A | 5 | a0001c0002t0001g0005 a0001c0002t0001g0059 a0001c0002t0001g0101 others(2): Show |
6 | HG02155.hp1 NA18994.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+4690C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735333 | |||||||
chr16:74735382 | C | G | 20 | a0001c0001t0003g0129 a0001c0002t0003g0126 a0001c0002t0003g0128 others(17): Show |
21 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+4641G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735382 | |||||||
chr16:74735463 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.363+4560G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735463 | |||||||
chr16:74735792 | C | T | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.363+4231G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735792 | |||||||
chr16:74735932 | G | A | 1 | a0001c0003t0011g0356 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.363+4091C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74735932 | |||||||
chr16:74736058 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(100): Show |
106 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.363+3964delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736058 | |||||||
chr16:74736201 | C | T | 31 | a0001c0001t0001g0281 a0001c0001t0003g0013 a0001c0001t0003g0050 others(28): Show |
33 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.363+3822G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736201 | |||||||
chr16:74736393 | A | G | 363 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(360): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.363+3630T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736393 | |||||||
chr16:74736401 | G | C | 1 | a0001c0003t0009g0346 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3622C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736401 | |||||||
chr16:74736613 | C | T | 8 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(5): Show |
10 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+3410G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736613 | |||||||
chr16:74736761 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.363+3262G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736761 | |||||||
chr16:74736767 | C | T | 1 | a0001c0003t0009g0346 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.363+3256G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736767 | |||||||
chr16:74736778 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
219 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.363+3245A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736778 | |||||||
chr16:74736807 | T | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(76): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.363+3216A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736807 | |||||||
chr16:74736824 | T | C | 10 | a0001c0001t0001g0131 a0001c0001t0002g0159 a0001c0001t0005g0183 others(7): Show |
10 | HG02145.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+3199A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74736824 | |||||||
chr16:74737011 | G | C | 2 | a0001c0001t0001g0117 a0001c0002t0001g0118 |
2 | HG03831.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.363+3012C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737011 | |||||||
chr16:74737064 | C | T | 1 | a0001c0002t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+2959G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737064 | |||||||
chr16:74737085 | C | T | 1 | a0001c0003t0001g0336 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.363+2938G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737085 | |||||||
chr16:74737130 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.363+2893G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737130 | |||||||
chr16:74737154 | G | C | 2 | a0002c0009t0001g0208 a0002c0009t0001g0210 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.363+2869C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737154 | |||||||
chr16:74737242 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.363+2781C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737242 | |||||||
chr16:74737266 | G | A | 3 | a0001c0002t0001g0168 a0001c0002t0001g0269 a0001c0002t0006g0268 |
3 | HG02056.hp1 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.363+2757C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737266 | |||||||
chr16:74737441 | A | G | 1 | a0001c0004t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.363+2582T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737441 | |||||||
chr16:74737467 | G | A | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.363+2556C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737467 | |||||||
chr16:74737469 | G | A | 62 | a0001c0001t0001g0107 a0001c0001t0001g0149 a0001c0001t0001g0202 others(59): Show |
67 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.363+2554C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737469 | |||||||
chr16:74737480 | G | A | 1 | a0001c0003t0005g0361 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.363+2543C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737480 | |||||||
chr16:74737640 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.363+2383G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737640 | |||||||
chr16:74737642 | C | G | 1 | a0001c0005t0012g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363+2381G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737642 | |||||||
chr16:74737643 | C | T | 1 | a0001c0002t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.363+2380G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737643 | |||||||
chr16:74737685 | G | C | 166 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0107 others(163): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.363+2338C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737685 | |||||||
chr16:74737762 | GGCCT | G | 15 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(12): Show |
16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+2257_363+2260d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737762 | |||||||
chr16:74737776 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.363+2247G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737776 | |||||||
chr16:74737888 | A | C | 1 | a0001c0001t0003g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+2135T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737888 | |||||||
chr16:74737946 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
183 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.363+2077C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74737946 | |||||||
chr16:74738033 | G | A | 15 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(12): Show |
16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1990C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738033 | |||||||
chr16:74738082 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0001g0292 a0001c0001t0001g0296 |
3 | HG00738.hp1 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.363+1941C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738082 | |||||||
chr16:74738348 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(52): Show |
59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.363+1675C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738348 | |||||||
chr16:74738429 | G | A | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.363+1594C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738429 | |||||||
chr16:74738609 | C | A | 1 | a0001c0001t0003g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.363+1414G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738609 | |||||||
chr16:74738725 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.363+1298G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738725 | |||||||
chr16:74738746 | C | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1277G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738746 | |||||||
chr16:74738748 | C | G | 5 | a0001c0001t0001g0096 a0001c0001t0001g0288 a0001c0001t0001g0289 others(2): Show |
5 | HG01891.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1275G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738748 | |||||||
chr16:74738752 | CT | C | 15 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(12): Show |
16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1270delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738752 | |||||||
chr16:74738864 | G | A | 3 | a0001c0002t0001g0095 a0001c0002t0001g0119 a0001c0002t0001g0198 |
3 | NA18960.hp1 NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.363+1159C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738864 | |||||||
chr16:74738900 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(113): Show |
119 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.363+1123G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738900 | |||||||
chr16:74738953 | G | A | 15 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(12): Show |
16 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1070C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74738953 | |||||||
chr16:74739091 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(52): Show |
59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.363+932G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739091 | |||||||
chr16:74739332 | C | T | 1 | a0001c0001t0003g0186 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.363+691G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739332 | |||||||
chr16:74739337 | C | A | 1 | a0001c0002t0001g0021 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.363+686G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739337 | |||||||
chr16:74739338 | TCCCTCCA others(6): Show |
T | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.363+672_363+684del others(13): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739338 | |||||||
chr16:74739372 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.363+651C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739372 | |||||||
chr16:74739408 | C | A | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+615G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739408 | |||||||
chr16:74739428 | C | T | 1 | a0001c0005t0012g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.363+595G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739428 | |||||||
chr16:74739578 | G | A | 1 | a0001c0008t0009g0366 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.363+445C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739578 | |||||||
chr16:74739874 | G | A | 3 | a0001c0002t0003g0126 a0001c0002t0003g0128 a0001c0002t0003g0130 |
3 | HG02965.hp1 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.363+149C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739874 | |||||||
chr16:74739917 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0164 |
2 | NA18960.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.363+106A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74739917 | |||||||
chr16:74740006 | C | A | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+17G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 2/6 | chr16 | 74740006 | |||||||
chr16:74740250 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.271-135C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740250 | |||||||
chr16:74740481 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.271-366C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740481 | |||||||
chr16:74740521 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(114): Show |
120 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.271-406C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740521 | |||||||
chr16:74740534 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18966.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.271-419G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740534 | |||||||
chr16:74740584 | A | T | 4 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-469T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740584 | |||||||
chr16:74740606 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.271-491T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740606 | |||||||
chr16:74740620 | A | AAAT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(87): Show |
97 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.271-508_271-506dup others(3): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | A | AAATAAT | 28 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0091 others(25): Show |
28 | HG00408.hp2 HG00438.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.271-511_271-506dup others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | A | AAATAATA others(2): Show |
9 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0264 others(6): Show |
10 | HG00099.hp2 HG01516.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-514_271-506dup others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | A | T | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-505T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | AAAT | A | 22 | a0001c0001t0001g0071 a0001c0001t0001g0281 a0001c0001t0003g0050 others(19): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.271-508_271-506del others(3): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | AAATAAT | A | 49 | a0001c0001t0001g0131 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
51 | HG00621.hp2 HG00639.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.271-511_271-506del others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | AAATAATA others(2): Show |
A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0107 others(83): Show |
94 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.271-514_271-506del others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | AAATAATA others(5): Show |
A | 3 | a0001c0003t0002g0357 a0001c0003t0005g0362 a0001c0003t0011g0356 |
3 | HG02922.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-517_271-506del others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740620 | AAATAATA others(8): Show |
A | 5 | a0001c0001t0001g0167 a0001c0001t0001g0242 a0001c0002t0001g0269 others(2): Show |
5 | HG01123.hp1 HG02056.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-520_271-506del others(15): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740620 | |||||||
chr16:74740673 | T | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(53): Show |
60 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.271-558A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740673 | |||||||
chr16:74740876 | A | G | 6 | a0001c0001t0001g0032 a0001c0007t0001g0007 a0001c0007t0001g0041 others(3): Show |
7 | HG02071.hp1 HG02155.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-761T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740876 | |||||||
chr16:74740991 | G | A | 2 | a0002c0009t0012g0094 a0002c0020t0017g0353 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.271-876C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74740991 | |||||||
chr16:74741117 | G | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(342): Show |
365 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.271-1002C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741117 | |||||||
chr16:74741140 | G | A | 4 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1025C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741140 | |||||||
chr16:74741381 | A | G | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-1266T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741381 | |||||||
chr16:74741519 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.271-1404G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741519 | |||||||
chr16:74741557 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.271-1442G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741557 | |||||||
chr16:74741773 | A | AAT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0071 others(6): Show |
12 | HG00280.hp1 HG00408.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-1660_271-1659d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATAT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0067 others(14): Show |
19 | HG00280.hp2 HG01109.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.271-1662_271-1659d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATAT | 3 | a0001c0001t0001g0066 a0001c0001t0003g0051 a0001c0003t0001g0326 |
3 | HG02698.hp2 HG03942.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.271-1664_271-1659d others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATATA others(1): Show |
16 | a0001c0001t0003g0129 a0001c0001t0003g0240 a0001c0001t0023g0291 others(13): Show |
16 | HG00639.hp1 HG01074.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-1666_271-1659d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATATA others(3): Show |
3 | a0001c0001t0003g0204 a0001c0002t0015g0193 a0001c0003t0001g0336 |
3 | HG02258.hp1 HG02683.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.271-1668_271-1659d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATATA others(5): Show |
5 | a0001c0001t0001g0096 a0001c0001t0001g0288 a0001c0004t0007g0088 others(2): Show |
5 | HG01069.hp2 HG01891.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-1670_271-1659d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATATA others(7): Show |
4 | a0001c0001t0001g0292 a0001c0003t0001g0311 a0001c0003t0002g0338 others(1): Show |
4 | HG00099.hp2 HG01257.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1672_271-1659d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | AATATATA others(9): Show |
1 | a0001c0003t0001g0301 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.271-1674_271-1659d others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271-1659_271-1658i others(17): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | A | T | 1 | a0001c0013t0001g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.271-1658T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | AAT | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0029 others(17): Show |
20 | HG01975.hp1 HG01978.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-1660_271-1659d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | AATAT | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0074 a0001c0003t0003g0017 others(2): Show |
7 | HG01358.hp1 HG02074.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1662_271-1659d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741773 | AATATATA others(3): Show |
A | 1 | a0001c0001t0006g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.271-1668_271-1659d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741773 | |||||||
chr16:74741796 | ATATATAT others(7): Show |
A | 1 | a0001c0004t0007g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-1695_271-1682d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741796 | |||||||
chr16:74741800 | ATATATAT others(5): Show |
A | 1 | a0001c0007t0001g0007 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.271-1697_271-1686d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741800 | |||||||
chr16:74741800 | ATATATAT others(7): Show |
A | 6 | a0001c0003t0001g0313 a0001c0003t0001g0314 a0001c0003t0001g0315 others(3): Show |
6 | HG02280.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1699_271-1686d others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741800 | |||||||
chr16:74741802 | ATATATAT others(3): Show |
A | 1 | a0001c0003t0001g0352 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.271-1697_271-1688d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741802 | |||||||
chr16:74741802 | ATATATAT others(5): Show |
A | 24 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0089 others(21): Show |
24 | HG00408.hp2 HG00438.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.271-1699_271-1688d others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741802 | |||||||
chr16:74741804 | A | ATG | 6 | a0001c0001t0002g0006 a0001c0002t0001g0119 a0001c0002t0001g0198 others(3): Show |
7 | HG01358.hp2 HG01496.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1690_271-1689i others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | |||||||
chr16:74741804 | A | ATGTG | 8 | a0001c0001t0001g0167 a0001c0002t0001g0034 a0001c0002t0001g0112 others(5): Show |
8 | HG01123.hp1 HG01361.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-1690_271-1689i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | |||||||
chr16:74741804 | A | G | 4 | a0001c0001t0002g0010 a0001c0002t0001g0095 a0001c0002t0001g0123 others(1): Show |
4 | HG02735.hp1 HG03041.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1689T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | |||||||
chr16:74741804 | ATATATGT others(1): Show |
A | 4 | a0001c0001t0001g0234 a0001c0001t0003g0227 a0001c0001t0018g0267 others(1): Show |
4 | HG01071.hp1 HG03239.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1697_271-1690d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | |||||||
chr16:74741804 | ATATATGT others(3): Show |
A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0064 others(11): Show |
15 | HG01109.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-1699_271-1690d others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741804 | |||||||
chr16:74741806 | A | ATG | 5 | a0001c0001t0002g0010 a0001c0002t0001g0002 a0001c0002t0001g0118 others(2): Show |
5 | HG00544.hp1 HG01123.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | |||||||
chr16:74741806 | A | ATGTG | 24 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0255 others(21): Show |
25 | HG00597.hp1 HG01069.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | |||||||
chr16:74741806 | A | ATGTGTG | 4 | a0001c0001t0003g0224 a0001c0002t0001g0153 a0001c0002t0001g0168 others(1): Show |
4 | HG01934.hp1 HG03017.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1692_271-1691i others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | |||||||
chr16:74741806 | A | G | 22 | a0001c0001t0001g0167 a0001c0001t0002g0006 a0001c0001t0002g0010 others(19): Show |
23 | HG01123.hp1 HG01358.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-1691T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741806 | |||||||
chr16:74741808 | A | ATATATAT others(19): Show |
1 | a0001c0004t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(28): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(21): Show |
1 | a0001c0002t0001g0192 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(30): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
2 | a0001c0001t0003g0197 a0001c0019t0016g0359 |
2 | HG01884.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(13): Show |
1 | a0001c0005t0010g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(11): Show |
1 | a0001c0005t0012g0360 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0277 a0001c0003t0002g0016 |
3 | HG00738.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(15): Show |
2 | a0001c0002t0001g0145 a0001c0003t0003g0344 |
2 | HG02738.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
1 | a0001c0006t0002g0339 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0155 a0001c0002t0001g0147 |
2 | HG00642.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(15): Show |
1 | a0001c0001t0005g0183 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
1 | a0001c0003t0005g0363 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(7): Show |
2 | a0002c0016t0001g0209 a0002c0017t0021g0027 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(9): Show |
1 | a0001c0006t0002g0331 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(11): Show |
5 | a0001c0001t0030g0156 a0001c0003t0005g0361 a0001c0004t0004g0274 others(2): Show |
5 | HG00323.hp1 HG00735.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(17): Show |
1 | a0001c0001t0024g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0131 a0005c0021t0001g0367 |
2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(9): Show |
1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0202 a0001c0003t0005g0362 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(3): Show |
7 | a0001c0001t0001g0278 a0001c0001t0001g0282 a0001c0001t0001g0289 others(4): Show |
7 | HG02698.hp1 HG02809.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0149 a0001c0002t0001g0125 |
2 | HG00642.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(7): Show |
2 | a0001c0003t0003g0335 a0001c0008t0027g0340 |
2 | HG01256.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.271-1694_271-1693i others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATAT others(5): Show |
2 | a0001c0002t0001g0146 a0001c0002t0001g0172 |
2 | HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATATGT others(3): Show |
2 | a0001c0001t0001g0008 a0001c0004t0019g0276 |
2 | HG02486.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATGTG | 3 | a0001c0001t0001g0150 a0001c0001t0003g0270 a0001c0002t0001g0175 |
3 | HG02155.hp1 HG03209.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.271-1694_271-1693i others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATATGTGT others(1): Show |
12 | a0001c0001t0001g0108 a0001c0001t0001g0151 a0001c0001t0001g0152 others(9): Show |
13 | HG01952.hp2 HG01975.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-1694_271-1693i others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATGTG | 5 | a0001c0001t0001g0097 a0001c0002t0001g0005 a0001c0002t0001g0101 others(2): Show |
6 | NA18960.hp2 NA18963.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1697_271-1694d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATGTGTG | 17 | a0001c0001t0001g0008 a0001c0001t0001g0200 a0001c0001t0002g0009 others(14): Show |
18 | HG00099.hp1 HG00140.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-1699_271-1694d others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | ATGTGTGT others(1): Show |
4 | a0001c0001t0002g0054 a0001c0002t0001g0055 a0001c0002t0008g0169 others(1): Show |
4 | HG02486.hp2 NA18612.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-1701_271-1694d others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741808 | A | G | 77 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0076 others(74): Show |
83 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.271-1693T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741808 | |||||||
chr16:74741810 | G | A | 40 | a0001c0001t0001g0056 a0001c0001t0001g0139 a0001c0001t0001g0196 others(37): Show |
40 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.271-1695C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741810 | |||||||
chr16:74741812 | G | A | 19 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(16): Show |
19 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.271-1697C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741812 | |||||||
chr16:74741814 | G | A | 7 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0264 others(4): Show |
7 | HG00609.hp2 HG02451.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1699C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741814 | |||||||
chr16:74741816 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1701C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741816 | |||||||
chr16:74741818 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1703C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741818 | |||||||
chr16:74741828 | GTGTGTGT others(4): Show |
G | 16 | a0001c0001t0001g0062 a0001c0001t0001g0137 a0001c0001t0001g0188 others(13): Show |
16 | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-1724_271-1714d others(13): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741828 | |||||||
chr16:74741829 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0030g0156 |
2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-1714A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741829 | |||||||
chr16:74741830 | GTGTGTGT others(2): Show |
G | 29 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0046 others(26): Show |
30 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.271-1724_271-1716d others(11): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741830 | |||||||
chr16:74741832 | GTGTGTAT | G | 10 | a0001c0001t0001g0056 a0001c0001t0001g0139 a0001c0001t0001g0229 others(7): Show |
10 | HG01081.hp1 HG02132.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-1724_271-1718d others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741832 | |||||||
chr16:74741834 | GTGTAT | G | 10 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0002g0037 others(7): Show |
10 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1724_271-1720d others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741834 | |||||||
chr16:74741836 | GTAT | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(50): Show |
55 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.271-1724_271-1722d others(5): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741836 | |||||||
chr16:74741838 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.271-1723T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741838 | |||||||
chr16:74741862 | G | GTGTA | 3 | a0001c0001t0001g0131 a0001c0001t0002g0159 a0005c0021t0001g0367 |
3 | HG03098.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.271-1748_271-1747i others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74741862 | |||||||
chr16:74742126 | A | G | 1 | a0001c0002t0002g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.271-2011T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742126 | |||||||
chr16:74742166 | C | A | 1 | a0001c0001t0030g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.271-2051G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742166 | |||||||
chr16:74742239 | C | T | 4 | a0001c0003t0009g0346 a0001c0003t0009g0347 a0001c0008t0009g0365 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2124G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742239 | |||||||
chr16:74742273 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
199 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.271-2158C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742273 | |||||||
chr16:74742364 | C | T | 9 | a0001c0001t0001g0096 a0001c0001t0001g0131 a0001c0001t0002g0159 others(6): Show |
9 | HG02622.hp1 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-2249G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742364 | |||||||
chr16:74742438 | A | T | 1 | a0001c0005t0004g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.271-2323T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742438 | |||||||
chr16:74742532 | G | T | 1 | a0001c0001t0002g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.271-2417C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742532 | |||||||
chr16:74742730 | C | T | 4 | a0001c0001t0005g0183 a0001c0003t0005g0361 a0001c0003t0005g0362 others(1): Show |
4 | HG02647.hp2 HG02922.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2615G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742730 | |||||||
chr16:74742944 | T | C | 1 | a0001c0002t0001g0198 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.271-2829A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74742944 | |||||||
chr16:74743183 | A | G | 1 | a0001c0001t0028g0053 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.271-3068T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743183 | |||||||
chr16:74743194 | A | T | 2 | a0001c0003t0001g0321 a0001c0003t0002g0320 |
2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3079T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743194 | |||||||
chr16:74743431 | C | T | 1 | a0001c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.271-3316G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743431 | |||||||
chr16:74743498 | T | C | 2 | a0001c0001t0002g0155 a0001c0001t0030g0156 |
2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-3383A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743498 | |||||||
chr16:74743540 | T | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0002g0290 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3425A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743540 | |||||||
chr16:74743569 | A | C | 4 | a0001c0003t0009g0346 a0001c0003t0009g0347 a0001c0008t0009g0365 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3454T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743569 | |||||||
chr16:74743650 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0030g0156 |
2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-3535C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743650 | |||||||
chr16:74743700 | G | T | 1 | a0001c0001t0003g0227 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.271-3585C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743700 | |||||||
chr16:74743704 | C | A | 1 | a0001c0001t0024g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.271-3589G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743704 | |||||||
chr16:74743805 | C | T | 3 | a0001c0001t0003g0011 a0001c0001t0003g0185 a0001c0001t0003g0186 |
4 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3690G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743805 | |||||||
chr16:74743896 | G | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(111): Show |
117 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.271-3781C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74743896 | |||||||
chr16:74744027 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.271-3912G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744027 | |||||||
chr16:74744065 | G | A | 2 | a0001c0003t0002g0357 a0001c0003t0011g0356 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271-3950C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744065 | |||||||
chr16:74744108 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(190): Show |
200 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.271-3993C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744108 | |||||||
chr16:74744140 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.271-4025C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744140 | |||||||
chr16:74744232 | T | C | 1 | a0001c0001t0011g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.271-4117A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744232 | |||||||
chr16:74744264 | C | A | 16 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(13): Show |
17 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.271-4149G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744264 | |||||||
chr16:74744265 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(52): Show |
59 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.271-4150G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744265 | |||||||
chr16:74744394 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271-4279T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744394 | |||||||
chr16:74744450 | C | CT | 12 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0082 others(9): Show |
12 | HG01934.hp1 HG02074.hp1 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-4336dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | |||||||
chr16:74744450 | CT | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0038 others(60): Show |
65 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.271-4336delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | |||||||
chr16:74744450 | CTT | C | 78 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0046 others(75): Show |
79 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.271-4337_271-4336d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744450 | |||||||
chr16:74744530 | C | T | 1 | a0001c0003t0002g0320 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271-4415G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744530 | |||||||
chr16:74744708 | T | A | 3 | a0001c0001t0001g0038 a0001c0001t0002g0246 a0001c0001t0002g0247 |
3 | HG02015.hp1 NA18965.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.271-4593A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744708 | |||||||
chr16:74744877 | C | T | 4 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4762G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744877 | |||||||
chr16:74744986 | G | C | 4 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-4871C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74744986 | |||||||
chr16:74745012 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
35 | HG00621.hp1 HG01975.hp1 HG02040.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-4897C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745012 | |||||||
chr16:74745072 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271-4957A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745072 | |||||||
chr16:74745194 | T | C | 2 | a0001c0005t0010g0318 a0001c0005t0010g0319 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.271-5079A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745194 | |||||||
chr16:74745378 | G | T | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-5263C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745378 | |||||||
chr16:74745485 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0002g0006 a0001c0001t0002g0009 others(5): Show |
10 | HG01358.hp2 HG01496.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-5370G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745485 | |||||||
chr16:74745517 | C | A | 11 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(8): Show |
12 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-5402G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745517 | |||||||
chr16:74745577 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.271-5462T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745577 | |||||||
chr16:74745740 | C | T | 1 | a0001c0004t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.271-5625G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745740 | |||||||
chr16:74745799 | A | AT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0065 others(11): Show |
14 | HG01981.hp1 HG02145.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-5685dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | |||||||
chr16:74745799 | AT | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(265): Show |
287 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.271-5685delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | |||||||
chr16:74745799 | ATT | A | 12 | a0001c0001t0001g0091 a0001c0001t0001g0229 a0001c0001t0001g0281 others(9): Show |
12 | HG00140.hp2 HG01928.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-5686_271-5685d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745799 | |||||||
chr16:74745937 | T | C | 143 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0107 others(140): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.271-5822A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74745937 | |||||||
chr16:74746054 | G | A | 140 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0107 others(137): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.271-5939C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746054 | |||||||
chr16:74746069 | G | T | 2 | a0001c0001t0002g0155 a0001c0001t0030g0156 |
2 | HG00323.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.271-5954C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746069 | |||||||
chr16:74746372 | A | AT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0066 a0001c0001t0001g0069 others(3): Show |
7 | NA19002.hp1 NA19007.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-6258dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746372 | |||||||
chr16:74746374 | TA | T | 13 | a0001c0001t0001g0167 a0001c0002t0001g0119 a0001c0002t0002g0287 others(10): Show |
15 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-6260delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746374 | |||||||
chr16:74746375 | A | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(47): Show |
51 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.271-6260T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746375 | |||||||
chr16:74746376 | TTA | T | 14 | a0001c0001t0001g0281 a0001c0001t0003g0050 a0001c0001t0003g0051 others(11): Show |
14 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-6263_271-6262d others(4): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746376 | |||||||
chr16:74746377 | TA | T | 139 | a0001c0001t0001g0008 a0001c0001t0001g0081 a0001c0001t0001g0097 others(136): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.271-6263delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746377 | |||||||
chr16:74746378 | A | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0023 others(95): Show |
105 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.271-6263T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746378 | |||||||
chr16:74746516 | G | A | 16 | a0001c0003t0001g0301 a0001c0003t0001g0311 a0001c0003t0002g0016 others(13): Show |
17 | HG00099.hp2 HG01069.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.271-6401C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746516 | |||||||
chr16:74746592 | C | A | 11 | a0001c0001t0002g0054 a0001c0001t0002g0246 a0001c0001t0002g0247 others(8): Show |
11 | HG00597.hp1 HG02015.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.271-6477G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746592 | |||||||
chr16:74746961 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0033 others(119): Show |
125 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.271-6846G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74746961 | |||||||
chr16:74747184 | A | T | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-7069T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747184 | |||||||
chr16:74747251 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.271-7136G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747251 | |||||||
chr16:74747331 | TAAGA | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(351): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.271-7220_271-7217d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747331 | |||||||
chr16:74747334 | G | A | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.271-7219C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747334 | |||||||
chr16:74747335 | A | T | 1 | a0001c0001t0003g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.271-7220T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747335 | |||||||
chr16:74747355 | A | G | 1 | a0001c0004t0007g0088 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.271-7240T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747355 | |||||||
chr16:74747419 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.271-7304C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747419 | |||||||
chr16:74747618 | C | T | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.271-7503G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747618 | |||||||
chr16:74747619 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(283): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.271-7504T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747619 | |||||||
chr16:74747896 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(116): Show |
121 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.271-7781G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74747896 | |||||||
chr16:74748216 | G | C | 361 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(358): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.271-8101C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748216 | |||||||
chr16:74748254 | C | T | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-8139G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748254 | |||||||
chr16:74748350 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.271-8235A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748350 | |||||||
chr16:74748542 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(61): Show |
71 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.271-8427C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748542 | |||||||
chr16:74748777 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.271-8662A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748777 | |||||||
chr16:74748793 | G | A | 1 | a0003c0011t0020g0019 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.271-8678C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748793 | |||||||
chr16:74748956 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
39 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(36): Show |
intron_variant | MODIFIER | c.271-8841C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74748956 | |||||||
chr16:74749160 | G | C | 1 | a0001c0002t0001g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.271-9045C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749160 | |||||||
chr16:74749372 | C | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(167): Show |
175 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.271-9257G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749372 | |||||||
chr16:74749393 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271-9278G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749393 | |||||||
chr16:74749462 | G | A | 6 | a0001c0003t0003g0317 a0001c0005t0004g0316 a0001c0005t0010g0318 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-9347C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749462 | |||||||
chr16:74749467 | C | A | 1 | a0001c0003t0001g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.271-9352G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749467 | |||||||
chr16:74749500 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(111): Show |
117 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.271-9385T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749500 | |||||||
chr16:74749582 | T | A | 58 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(55): Show |
60 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.271-9467A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749582 | |||||||
chr16:74749851 | G | A | 8 | a0001c0001t0001g0296 a0001c0001t0003g0271 a0001c0003t0001g0352 others(5): Show |
9 | HG02145.hp2 HG02922.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-9736C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749851 | |||||||
chr16:74749864 | G | A | 1 | a0001c0001t0014g0039 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.271-9749C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749864 | |||||||
chr16:74749871 | T | C | 2 | a0001c0008t0009g0365 a0001c0008t0009g0366 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.271-9756A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74749871 | |||||||
chr16:74750233 | G | A | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-10118C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750233 | |||||||
chr16:74750271 | G | A | 4 | a0001c0001t0003g0011 a0001c0001t0003g0185 a0001c0001t0003g0186 others(1): Show |
5 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-10156C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750271 | |||||||
chr16:74750421 | T | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(25): Show |
33 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.271-10306A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750421 | |||||||
chr16:74750517 | G | C | 1 | a0001c0001t0007g0221 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.271-10402C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750517 | |||||||
chr16:74750551 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-10436C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750551 | |||||||
chr16:74750761 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0030 a0001c0001t0001g0131 a0001c0003t0002g0348 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-10654_271-1064 others(12): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(3): Show |
12 | a0001c0001t0001g0029 a0001c0001t0002g0159 a0001c0003t0002g0357 others(9): Show |
12 | HG01069.hp2 HG02886.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-10656_271-1064 others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(5): Show |
15 | a0001c0001t0001g0026 a0001c0001t0001g0218 a0001c0001t0001g0242 others(12): Show |
15 | HG01071.hp1 HG01074.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-10658_271-1064 others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(7): Show |
58 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0032 others(55): Show |
61 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.271-10660_271-1064 others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(9): Show |
57 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(54): Show |
61 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.271-10662_271-1064 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(11): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0036 others(44): Show |
50 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.271-10664_271-1064 others(22): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(13): Show |
11 | a0001c0001t0001g0277 a0001c0001t0001g0279 a0001c0001t0001g0292 others(8): Show |
12 | HG00738.hp1 HG01358.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-10666_271-1064 others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | C | CTGTGTGT others(15): Show |
1 | a0001c0001t0001g0157 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.271-10668_271-1064 others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750761 | CTG | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0105 others(98): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.271-10648_271-1064 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750761 | |||||||
chr16:74750781 | G | GTGTGTGT others(5): Show |
14 | a0001c0003t0001g0301 a0001c0003t0001g0308 a0001c0003t0001g0309 others(11): Show |
15 | HG00099.hp2 HG01192.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.271-10667_271-1066 others(16): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | |||||||
chr16:74750781 | G | GTGTGTGT others(7): Show |
1 | a0001c0003t0001g0314 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.271-10667_271-1066 others(18): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | |||||||
chr16:74750781 | G | GTGTGTGT others(9): Show |
10 | a0001c0003t0001g0313 a0001c0003t0001g0315 a0001c0003t0003g0317 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-10667_271-1066 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | |||||||
chr16:74750781 | G | GTGTGTGT others(15): Show |
1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-10667_271-1066 others(26): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750781 | |||||||
chr16:74750790 | T | C | 2 | a0001c0008t0009g0365 a0001c0008t0009g0366 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.271-10675A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | |||||||
chr16:74750790 | T | TGTGTGC | 5 | a0001c0003t0005g0361 a0001c0003t0005g0363 a0001c0003t0009g0346 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-10676_271-1067 others(10): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | |||||||
chr16:74750790 | T | TGTGTGTG others(3): Show |
1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-10676_271-1067 others(14): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | |||||||
chr16:74750790 | T | TGTGTGTG others(10): Show |
2 | a0001c0001t0003g0215 a0001c0002t0002g0287 |
2 | HG01517.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.271-10676_271-1067 others(21): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | |||||||
chr16:74750790 | T | TGTGTGTG others(13): Show |
1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-10676_271-1067 others(24): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750790 | |||||||
chr16:74750857 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-10742G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750857 | |||||||
chr16:74750937 | A | G | 2 | a0001c0004t0004g0274 a0001c0004t0004g0294 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.271-10822T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74750937 | |||||||
chr16:74751129 | C | T | 1 | a0001c0002t0003g0297 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-11014G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751129 | |||||||
chr16:74751226 | C | A | 3 | a0001c0001t0001g0296 a0001c0001t0003g0271 a0001c0003t0002g0345 |
3 | HG02922.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.271-11111G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751226 | |||||||
chr16:74751272 | T | G | 1 | a0001c0002t0001g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.271-11157A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751272 | |||||||
chr16:74751286 | G | A | 96 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0105 others(93): Show |
105 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.271-11171C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751286 | |||||||
chr16:74751304 | C | T | 1 | a0001c0002t0003g0297 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-11189G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751304 | |||||||
chr16:74751428 | C | T | 1 | a0001c0003t0003g0343 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.271-11313G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751428 | |||||||
chr16:74751500 | C | A | 2 | a0001c0003t0005g0298 a0001c0003t0005g0354 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.271-11385G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751500 | |||||||
chr16:74751679 | C | CGGACAGC others(8): Show |
10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-11579_271-1156 others(19): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751679 | |||||||
chr16:74751888 | G | C | 65 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.271-11773C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751888 | |||||||
chr16:74751932 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
29 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.271-11817C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74751932 | |||||||
chr16:74752004 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(26): Show |
34 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.271-11889T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752004 | |||||||
chr16:74752134 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.271-12019G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752134 | |||||||
chr16:74752198 | C | G | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-12083G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752198 | |||||||
chr16:74752203 | G | A | 62 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12088C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752203 | |||||||
chr16:74752264 | A | T | 62 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12149T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752264 | |||||||
chr16:74752280 | G | C | 62 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12165C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752280 | |||||||
chr16:74752401 | C | T | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-12286G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752401 | |||||||
chr16:74752475 | G | T | 1 | a0001c0003t0009g0346 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271-12360C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752475 | |||||||
chr16:74752513 | A | T | 61 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(58): Show |
63 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.271-12398T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752513 | |||||||
chr16:74752550 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.271-12435A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752550 | |||||||
chr16:74752563 | G | C | 36 | a0001c0001t0001g0107 a0001c0001t0003g0197 a0001c0001t0003g0212 others(33): Show |
37 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.271-12448C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752563 | |||||||
chr16:74752595 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.271-12480G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752595 | |||||||
chr16:74752666 | G | C | 2 | a0001c0001t0001g0245 a0001c0001t0002g0244 |
2 | HG00738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.271-12551C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752666 | |||||||
chr16:74752718 | G | A | 62 | a0001c0001t0001g0091 a0001c0001t0001g0218 a0001c0001t0001g0222 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-12603C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74752718 | |||||||
chr16:74753101 | C | T | 30 | a0001c0001t0024g0028 a0001c0003t0001g0301 a0001c0003t0001g0308 others(27): Show |
32 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.271-12986G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753101 | |||||||
chr16:74753349 | C | T | 4 | a0001c0001t0002g0155 a0001c0001t0003g0154 a0001c0001t0003g0204 others(1): Show |
4 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-13234G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753349 | |||||||
chr16:74753445 | T | C | 2 | a0001c0001t0002g0246 a0001c0001t0002g0247 |
2 | HG02015.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.271-13330A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753445 | |||||||
chr16:74753453 | G | A | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.271-13338C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753453 | |||||||
chr16:74753456 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.271-13341A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753456 | |||||||
chr16:74753534 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.271-13419C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753534 | |||||||
chr16:74753654 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.271-13539G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753654 | |||||||
chr16:74753720 | G | C | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(74): Show |
79 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.271-13605C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753720 | |||||||
chr16:74753777 | G | A | 105 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0001g0218 others(102): Show |
109 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-13662C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753777 | |||||||
chr16:74753821 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.271-13706A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753821 | |||||||
chr16:74753941 | G | A | 62 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0218 others(59): Show |
64 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.271-13826C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753941 | |||||||
chr16:74753954 | T | C | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.271-13839A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74753954 | |||||||
chr16:74754087 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(31): Show |
35 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-13972C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754087 | |||||||
chr16:74754108 | T | C | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-13993A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754108 | |||||||
chr16:74754110 | T | C | 7 | a0001c0003t0002g0348 a0001c0003t0002g0349 a0001c0003t0002g0350 others(4): Show |
7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-13995A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754110 | |||||||
chr16:74754134 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.271-14019C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754134 | |||||||
chr16:74754148 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271-14033G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754148 | |||||||
chr16:74754201 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.271-14086C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754201 | |||||||
chr16:74754201 | G | T | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-14086C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754201 | |||||||
chr16:74754255 | G | C | 4 | a0001c0001t0001g0222 a0001c0001t0003g0248 a0001c0001t0003g0249 others(1): Show |
4 | HG03710.hp2 HG03831.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-14140C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754255 | |||||||
chr16:74754404 | A | G | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-14289T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754404 | |||||||
chr16:74754431 | T | A | 1 | a0001c0002t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-14316A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754431 | |||||||
chr16:74754433 | T | C | 2 | a0001c0001t0003g0090 a0001c0001t0003g0270 |
2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.271-14318A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754433 | |||||||
chr16:74754484 | G | A | 26 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(23): Show |
27 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.271-14369C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754484 | |||||||
chr16:74754613 | T | C | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271-14498A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754613 | |||||||
chr16:74754739 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.271-14624C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754739 | |||||||
chr16:74754789 | A | G | 1 | a0001c0001t0001g0008 | 2 | NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.271-14674T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754789 | |||||||
chr16:74754853 | A | G | 1 | a0001c0002t0002g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.271-14738T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754853 | |||||||
chr16:74754909 | T | C | 32 | a0001c0001t0001g0296 a0001c0001t0003g0271 a0001c0003t0001g0301 others(29): Show |
34 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.271-14794A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754909 | |||||||
chr16:74754916 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-14801T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74754916 | |||||||
chr16:74755011 | C | G | 1 | a0001c0004t0004g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.271-14896G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755011 | |||||||
chr16:74755036 | C | T | 3 | a0001c0003t0001g0352 a0001c0008t0003g0351 a0002c0020t0017g0353 |
3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.271-14921G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755036 | |||||||
chr16:74755079 | C | G | 2 | a0001c0001t0001g0001 a0004c0015t0001g0295 |
5 | HG00280.hp1 HG01361.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-14964G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755079 | |||||||
chr16:74755120 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(15): Show |
21 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-15005G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755120 | |||||||
chr16:74755121 | G | A | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-15006C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755121 | |||||||
chr16:74755159 | G | GT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(126): Show |
133 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.271-15045dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755159 | |||||||
chr16:74755159 | G | GTT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0067 others(109): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.271-15046_271-1504 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755159 | |||||||
chr16:74755180 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.271-15065C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755180 | |||||||
chr16:74755489 | T | C | 1 | a0001c0001t0003g0216 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.271-15374A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755489 | |||||||
chr16:74755568 | A | C | 2 | a0001c0001t0024g0028 a0002c0017t0021g0027 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.271-15453T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755568 | |||||||
chr16:74755878 | T | TA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(111): Show |
118 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.271-15764dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74755878 | |||||||
chr16:74756158 | G | C | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.271-16043C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756158 | |||||||
chr16:74756172 | C | T | 2 | a0001c0003t0005g0298 a0001c0003t0005g0354 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.271-16057G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756172 | |||||||
chr16:74756177 | A | G | 1 | a0001c0002t0001g0153 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.271-16062T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756177 | |||||||
chr16:74756202 | C | T | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-16087G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756202 | |||||||
chr16:74756337 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.271-16222G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756337 | |||||||
chr16:74756386 | T | C | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.271-16271A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756386 | |||||||
chr16:74756600 | A | G | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-16485T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756600 | |||||||
chr16:74756644 | T | C | 31 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(28): Show |
33 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.271-16529A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756644 | |||||||
chr16:74756678 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.271-16563T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756678 | |||||||
chr16:74756734 | T | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0292 |
2 | HG00738.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.271-16619A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756734 | |||||||
chr16:74756760 | A | G | 4 | a0001c0003t0001g0352 a0001c0005t0013g0018 a0001c0008t0003g0351 others(1): Show |
5 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-16645T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756760 | |||||||
chr16:74756901 | A | G | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-16786T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74756901 | |||||||
chr16:74757144 | A | T | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271-17029T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757144 | |||||||
chr16:74757172 | A | G | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-17057T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757172 | |||||||
chr16:74757322 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.270+17164A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757322 | |||||||
chr16:74757402 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.270+17084A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757402 | |||||||
chr16:74757526 | G | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.270+16960C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757526 | |||||||
chr16:74757616 | T | C | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+16870A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757616 | |||||||
chr16:74757758 | T | A | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+16728A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757758 | |||||||
chr16:74757781 | C | G | 1 | a0001c0004t0004g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.270+16705G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757781 | |||||||
chr16:74757803 | G | A | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+16683C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757803 | |||||||
chr16:74757871 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(77): Show |
82 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+16615A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757871 | |||||||
chr16:74757929 | G | C | 27 | a0001c0003t0001g0301 a0001c0003t0001g0308 a0001c0003t0001g0309 others(24): Show |
28 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+16557C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74757929 | |||||||
chr16:74758091 | G | A | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+16395C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758091 | |||||||
chr16:74758117 | CT | C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0092 a0001c0001t0003g0050 others(11): Show |
14 | HG01515.hp2 HG02486.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.270+16368delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | |||||||
chr16:74758117 | CTT | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
145 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.270+16367_270+1636 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | |||||||
chr16:74758117 | CTTT | C | 35 | a0001c0001t0001g0091 a0001c0001t0001g0107 a0001c0001t0003g0197 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+16366_270+1636 others(7): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758117 | |||||||
chr16:74758143 | C | T | 57 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0001g0225 others(54): Show |
59 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.270+16343G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758143 | |||||||
chr16:74758160 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0266 |
2 | HG00609.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.270+16326C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758160 | |||||||
chr16:74758266 | G | A | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+16220C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758266 | |||||||
chr16:74758280 | C | T | 3 | a0001c0002t0001g0109 a0001c0002t0008g0110 a0001c0002t0029g0195 |
3 | NA18939.hp2 NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.270+16206G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758280 | |||||||
chr16:74758342 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+16144C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758342 | |||||||
chr16:74758345 | C | T | 2 | a0001c0001t0024g0028 a0002c0017t0021g0027 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+16141G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758345 | |||||||
chr16:74758440 | C | T | 7 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(4): Show |
9 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+16046G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758440 | |||||||
chr16:74758553 | A | C | 7 | a0001c0003t0002g0348 a0001c0003t0002g0349 a0001c0003t0002g0350 others(4): Show |
7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+15933T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758553 | |||||||
chr16:74758562 | G | A | 2 | a0001c0003t0005g0298 a0001c0003t0005g0354 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.270+15924C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758562 | |||||||
chr16:74758575 | C | CT | 4 | a0001c0003t0001g0352 a0001c0005t0013g0018 a0001c0008t0003g0351 others(1): Show |
5 | HG02145.hp2 HG03041.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+15910dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758575 | |||||||
chr16:74758655 | G | A | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+15831C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758655 | |||||||
chr16:74758723 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.270+15763G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758723 | |||||||
chr16:74758784 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(56): Show |
65 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.270+15702T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758784 | |||||||
chr16:74758912 | G | A | 1 | a0002c0009t0012g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.270+15574C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758912 | |||||||
chr16:74758961 | A | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.270+15525T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74758961 | |||||||
chr16:74759159 | G | C | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+15327C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759159 | |||||||
chr16:74759383 | G | C | 1 | a0001c0002t0001g0184 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.270+15103C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759383 | |||||||
chr16:74759746 | T | C | 8 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0288 others(5): Show |
8 | HG00738.hp1 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+14740A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759746 | |||||||
chr16:74759778 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.270+14708G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759778 | |||||||
chr16:74759796 | T | G | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+14690A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759796 | |||||||
chr16:74759818 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.270+14668G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759818 | |||||||
chr16:74759993 | G | A | 5 | a0001c0003t0001g0308 a0001c0003t0001g0309 a0001c0003t0001g0310 others(2): Show |
5 | HG02040.hp2 NA18966.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+14493C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74759993 | |||||||
chr16:74760155 | T | C | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+14331A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760155 | |||||||
chr16:74760157 | C | T | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+14329G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760157 | |||||||
chr16:74760167 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0025 others(35): Show |
40 | HG00621.hp1 HG01069.hp2 HG01975.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+14319G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760167 | |||||||
chr16:74760350 | C | A | 7 | a0001c0004t0004g0014 a0001c0004t0004g0015 a0001c0004t0004g0205 others(4): Show |
9 | HG01069.hp1 HG01071.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+14136G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760350 | |||||||
chr16:74760393 | A | G | 1 | a0001c0004t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.270+14093T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760393 | |||||||
chr16:74760420 | G | A | 2 | a0001c0003t0001g0352 a0001c0008t0003g0351 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+14066C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760420 | |||||||
chr16:74760567 | T | A | 2 | a0001c0001t0003g0271 a0001c0003t0002g0345 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.270+13919A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760567 | |||||||
chr16:74760573 | G | A | 30 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(27): Show |
31 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.270+13913C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760573 | |||||||
chr16:74760599 | C | T | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+13887G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760599 | |||||||
chr16:74760600 | C | CA | 58 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0001g0225 others(55): Show |
60 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.270+13885dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760600 | |||||||
chr16:74760610 | C | G | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+13876G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760610 | |||||||
chr16:74760666 | T | A | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+13820A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760666 | |||||||
chr16:74760853 | T | C | 1 | a0001c0002t0001g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.270+13633A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74760853 | |||||||
chr16:74761174 | G | A | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+13312C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761174 | |||||||
chr16:74761367 | C | A | 1 | a0001c0001t0001g0067 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.270+13119G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761367 | |||||||
chr16:74761368 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+13118C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761368 | |||||||
chr16:74761452 | CA | C | 7 | a0001c0003t0002g0348 a0001c0003t0002g0349 a0001c0003t0002g0350 others(4): Show |
7 | HG01891.hp1 HG02976.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.270+13033delT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761452 | |||||||
chr16:74761458 | A | AAAAG | 8 | a0001c0001t0001g0008 a0001c0001t0001g0149 a0001c0001t0001g0150 others(5): Show |
9 | HG01884.hp1 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+13024_270+1302 others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | |||||||
chr16:74761458 | AAAAG | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(173): Show |
182 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.270+13024_270+1302 others(8): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | |||||||
chr16:74761458 | AAAAGAAA others(9): Show |
A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(55): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.270+13012_270+1302 others(20): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761458 | |||||||
chr16:74761461 | AGAAAG | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0096 others(1): Show |
4 | HG02622.hp1 HG03490.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+13020_270+1302 others(9): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761461 | |||||||
chr16:74761466 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(173): Show |
182 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.270+13020C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761466 | |||||||
chr16:74761470 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.270+13016C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761470 | |||||||
chr16:74761492 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12994G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761492 | |||||||
chr16:74761622 | T | C | 2 | a0001c0003t0003g0343 a0001c0003t0003g0344 |
2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.270+12864A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761622 | |||||||
chr16:74761805 | A | T | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+12681T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761805 | |||||||
chr16:74761909 | C | T | 30 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(27): Show |
31 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.270+12577G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761909 | |||||||
chr16:74761956 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+12530G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761956 | |||||||
chr16:74761971 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.270+12515C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74761971 | |||||||
chr16:74762058 | T | A | 2 | a0001c0008t0009g0365 a0001c0008t0009g0366 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+12428A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762058 | |||||||
chr16:74762076 | A | ACT | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12408_270+1240 others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762076 | |||||||
chr16:74762174 | G | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12312C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762174 | |||||||
chr16:74762175 | T | C | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+12311A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762175 | |||||||
chr16:74762234 | G | A | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+12252C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762234 | |||||||
chr16:74762264 | C | T | 27 | a0001c0003t0001g0301 a0001c0003t0001g0308 a0001c0003t0001g0309 others(24): Show |
28 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+12222G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762264 | |||||||
chr16:74762290 | G | A | 4 | a0001c0001t0003g0011 a0001c0001t0003g0185 a0001c0001t0003g0186 others(1): Show |
5 | NA19009.hp2 NA19064.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+12196C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762290 | |||||||
chr16:74762323 | G | A | 2 | a0001c0003t0009g0346 a0001c0003t0009g0347 |
2 | HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.270+12163C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762323 | |||||||
chr16:74762333 | G | A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(73): Show |
78 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.270+12153C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762333 | |||||||
chr16:74762388 | C | T | 2 | a0001c0001t0001g0033 a0001c0002t0001g0034 |
2 | NA18972.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.270+12098G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762388 | |||||||
chr16:74762410 | A | C | 1 | a0001c0003t0002g0327 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.270+12076T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762410 | |||||||
chr16:74762436 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+12050T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762436 | |||||||
chr16:74762534 | G | C | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+11952C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762534 | |||||||
chr16:74762617 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.270+11869C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762617 | |||||||
chr16:74762617 | G | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+11869C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762617 | |||||||
chr16:74762692 | G | A | 1 | a0001c0005t0010g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.270+11794C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762692 | |||||||
chr16:74762732 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11754T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762732 | |||||||
chr16:74762820 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11666T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762820 | |||||||
chr16:74762838 | A | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.270+11648T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762838 | |||||||
chr16:74762844 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 |
4 | HG02165.hp1 NA18994.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+11642T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762844 | |||||||
chr16:74762860 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.270+11626T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762860 | |||||||
chr16:74762864 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.270+11622C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762864 | |||||||
chr16:74762936 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(76): Show |
81 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.270+11550C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74762936 | |||||||
chr16:74763095 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11391C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763095 | |||||||
chr16:74763239 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+11247T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763239 | |||||||
chr16:74763268 | T | C | 1 | a0001c0002t0001g0269 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+11218A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763268 | |||||||
chr16:74763278 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.270+11208C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763278 | |||||||
chr16:74763383 | G | C | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+11103C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763383 | |||||||
chr16:74763404 | C | G | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+11082G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763404 | |||||||
chr16:74763405 | G | T | 19 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0135 others(16): Show |
20 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.270+11081C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763405 | |||||||
chr16:74763414 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(24): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+11072G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763414 | |||||||
chr16:74763418 | C | T | 17 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(14): Show |
17 | HG00621.hp2 HG00639.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+11068G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763418 | |||||||
chr16:74763446 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(89): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+11040G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763446 | |||||||
chr16:74763494 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.270+10992C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763494 | |||||||
chr16:74763496 | G | A | 10 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+10990C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763496 | |||||||
chr16:74763500 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.270+10986G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763500 | |||||||
chr16:74763584 | T | C | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+10902A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763584 | |||||||
chr16:74763689 | C | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(76): Show |
81 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.270+10797G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763689 | |||||||
chr16:74763701 | A | T | 20 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0135 others(17): Show |
21 | HG01928.hp1 HG01952.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.270+10785T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763701 | |||||||
chr16:74763708 | T | TC | 92 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(89): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+10777dupG | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763708 | |||||||
chr16:74763746 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+10740C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763746 | |||||||
chr16:74763786 | C | G | 2 | a0001c0001t0024g0028 a0002c0017t0021g0027 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+10700G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763786 | |||||||
chr16:74763904 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0107 a0001c0001t0001g0277 others(99): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.270+10582T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763904 | |||||||
chr16:74763982 | T | C | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270+10504A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763982 | |||||||
chr16:74763983 | T | C | 26 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(23): Show |
27 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.270+10503A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74763983 | |||||||
chr16:74764075 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.270+10411A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764075 | |||||||
chr16:74764399 | C | T | 1 | a0001c0002t0001g0133 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.270+10087G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764399 | |||||||
chr16:74764400 | G | A | 1 | a0001c0002t0001g0121 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.270+10086C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764400 | |||||||
chr16:74764428 | T | C | 1 | a0001c0004t0025g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.270+10058A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764428 | |||||||
chr16:74764666 | C | T | 3 | a0001c0008t0009g0365 a0001c0008t0009g0366 a0001c0019t0016g0359 |
3 | HG01884.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+9820G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764666 | |||||||
chr16:74764667 | C | T | 1 | a0001c0002t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.270+9819G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764667 | |||||||
chr16:74764726 | T | TA | 33 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(30): Show |
35 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+9759dupT | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764726 | |||||||
chr16:74764832 | A | T | 3 | a0001c0001t0001g0131 a0001c0012t0001g0020 a0001c0014t0003g0132 |
3 | HG02109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.270+9654T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764832 | |||||||
chr16:74764896 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(78): Show |
83 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.270+9590A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764896 | |||||||
chr16:74764986 | C | T | 2 | a0001c0003t0001g0352 a0001c0008t0003g0351 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+9500G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74764986 | |||||||
chr16:74765022 | G | A | 2 | a0001c0003t0001g0311 a0001c0003t0002g0016 |
3 | HG00099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.270+9464C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765022 | |||||||
chr16:74765159 | C | CT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(89): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.270+9326dupA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765159 | |||||||
chr16:74765159 | CT | C | 59 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0001g0225 others(56): Show |
61 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.270+9326delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765159 | |||||||
chr16:74765220 | G | A | 1 | a0001c0003t0001g0312 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.270+9266C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765220 | |||||||
chr16:74765242 | C | T | 1 | a0001c0002t0003g0297 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.270+9244G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765242 | |||||||
chr16:74765305 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(24): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+9181G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765305 | |||||||
chr16:74765306 | G | A | 361 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(358): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.270+9180C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765306 | |||||||
chr16:74765601 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+8885G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765601 | |||||||
chr16:74765613 | C | A | 6 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+8873G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765613 | |||||||
chr16:74765638 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.270+8848C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765638 | |||||||
chr16:74765992 | A | G | 1 | a0001c0005t0013g0018 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.270+8494T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74765992 | |||||||
chr16:74766050 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(33): Show |
36 | HG00621.hp2 HG00639.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.270+8436C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766050 | |||||||
chr16:74766149 | A | G | 1 | a0001c0004t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+8337T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766149 | |||||||
chr16:74766151 | T | A | 1 | a0001c0004t0001g0063 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.270+8335A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766151 | |||||||
chr16:74766476 | A | C | 1 | a0001c0002t0003g0126 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.270+8010T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766476 | |||||||
chr16:74766492 | G | C | 1 | a0001c0002t0001g0253 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.270+7994C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766492 | |||||||
chr16:74766556 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(55): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.270+7930G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766556 | |||||||
chr16:74766588 | A | C | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+7898T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766588 | |||||||
chr16:74766642 | AG | A | 45 | a0001c0001t0001g0107 a0001c0001t0003g0271 a0001c0003t0001g0301 others(42): Show |
47 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.270+7843delC | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766642 | |||||||
chr16:74766651 | G | T | 1 | a0001c0005t0001g0358 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.270+7835C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766651 | |||||||
chr16:74766673 | T | C | 3 | a0001c0003t0001g0352 a0001c0008t0003g0351 a0002c0020t0017g0353 |
3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+7813A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766673 | |||||||
chr16:74766810 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.270+7676G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766810 | |||||||
chr16:74766819 | A | G | 4 | a0001c0001t0001g0196 a0001c0002t0001g0125 a0001c0002t0001g0191 others(1): Show |
4 | HG00642.hp1 HG00733.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+7667T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766819 | |||||||
chr16:74766915 | G | A | 3 | a0001c0003t0001g0352 a0001c0008t0003g0351 a0002c0020t0017g0353 |
3 | HG02145.hp2 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270+7571C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74766915 | |||||||
chr16:74767185 | T | G | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+7301A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767185 | |||||||
chr16:74767257 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.270+7229G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767257 | |||||||
chr16:74767262 | T | C | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+7224A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767262 | |||||||
chr16:74767282 | C | G | 2 | a0001c0001t0001g0107 a0001c0003t0005g0364 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.270+7204G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767282 | |||||||
chr16:74767318 | C | A | 2 | a0001c0005t0010g0323 a0001c0005t0010g0324 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.270+7168G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767318 | |||||||
chr16:74767412 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.270+7074T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767412 | |||||||
chr16:74767421 | G | A | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+7065C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767421 | |||||||
chr16:74767442 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0033 others(33): Show |
36 | HG00621.hp2 HG00639.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.270+7044G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767442 | |||||||
chr16:74767539 | C | T | 1 | a0001c0001t0008g0124 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.270+6947G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767539 | |||||||
chr16:74767717 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(74): Show |
79 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+6769C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767717 | |||||||
chr16:74767882 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+6604C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767882 | |||||||
chr16:74767883 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+6603A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767883 | |||||||
chr16:74767924 | C | T | 1 | a0001c0004t0006g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270+6562G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767924 | |||||||
chr16:74767976 | G | A | 1 | a0001c0003t0005g0363 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.270+6510C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74767976 | |||||||
chr16:74768013 | A | G | 79 | a0001c0001t0001g0107 a0001c0001t0003g0197 a0001c0001t0003g0212 others(76): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.270+6473T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768013 | |||||||
chr16:74768517 | C | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.270+5969G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768517 | |||||||
chr16:74768523 | A | C | 21 | a0001c0001t0001g0117 a0001c0002t0001g0002 a0001c0002t0001g0095 others(18): Show |
23 | HG00544.hp1 HG02071.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.270+5963T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768523 | |||||||
chr16:74768588 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0003g0254 |
2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.270+5898C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768588 | |||||||
chr16:74768622 | A | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(76): Show |
81 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.270+5864T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768622 | |||||||
chr16:74768693 | C | T | 27 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(24): Show |
28 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.270+5793G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768693 | |||||||
chr16:74768950 | T | C | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+5536A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768950 | |||||||
chr16:74768974 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+5512G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74768974 | |||||||
chr16:74769008 | G | A | 3 | a0001c0001t0001g0196 a0001c0002t0001g0191 a0001c0002t0001g0192 |
3 | HG00733.hp1 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.270+5478C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769008 | |||||||
chr16:74769028 | C | T | 16 | a0001c0003t0001g0301 a0001c0003t0001g0308 a0001c0003t0001g0309 others(13): Show |
17 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+5458G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769028 | |||||||
chr16:74769047 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.270+5439C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769047 | |||||||
chr16:74769154 | A | G | 2 | a0001c0008t0009g0365 a0001c0008t0009g0366 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.270+5332T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769154 | |||||||
chr16:74769177 | C | T | 32 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(29): Show |
34 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+5309G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769177 | |||||||
chr16:74769180 | C | G | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+5306G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769180 | |||||||
chr16:74769430 | A | T | 1 | a0001c0002t0001g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.270+5056T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769430 | |||||||
chr16:74769446 | C | T | 8 | a0001c0003t0002g0348 a0001c0003t0002g0349 a0001c0003t0002g0350 others(5): Show |
8 | HG01891.hp1 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+5040G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769446 | |||||||
chr16:74769492 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.270+4994A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769492 | |||||||
chr16:74769541 | C | A | 9 | a0001c0001t0001g0107 a0001c0003t0005g0361 a0001c0003t0005g0362 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+4945G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769541 | |||||||
chr16:74769541 | C | T | 1 | a0001c0005t0007g0325 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.270+4945G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769541 | |||||||
chr16:74769602 | A | C | 32 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(29): Show |
33 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+4884T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769602 | |||||||
chr16:74769616 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.270+4870T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769616 | |||||||
chr16:74769628 | C | T | 1 | a0001c0002t0015g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.270+4858G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769628 | |||||||
chr16:74769662 | A | T | 1 | a0001c0003t0001g0326 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.270+4824T>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769662 | |||||||
chr16:74769705 | G | C | 1 | a0001c0004t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.270+4781C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769705 | |||||||
chr16:74769729 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270+4757T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769729 | |||||||
chr16:74769766 | G | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(143): Show |
150 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.270+4720C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769766 | |||||||
chr16:74769826 | G | C | 1 | a0001c0002t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.270+4660C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769826 | |||||||
chr16:74769898 | C | T | 1 | a0001c0001t0002g0006 | 2 | HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.270+4588G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769898 | |||||||
chr16:74769969 | G | A | 1 | a0001c0002t0029g0195 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.270+4517C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74769969 | |||||||
chr16:74770026 | G | T | 1 | a0001c0004t0007g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.270+4460C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770026 | |||||||
chr16:74770074 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.270+4412G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770074 | |||||||
chr16:74770157 | A | C | 2 | a0001c0001t0024g0028 a0002c0017t0021g0027 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.270+4329T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770157 | |||||||
chr16:74770312 | G | C | 3 | a0001c0003t0001g0313 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG02280.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.270+4174C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770312 | |||||||
chr16:74770374 | T | G | 34 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(31): Show |
36 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+4112A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | |||||||
chr16:74770374 | T | TTTTG | 3 | a0002c0009t0001g0208 a0002c0009t0001g0210 a0002c0016t0001g0209 |
3 | HG02896.hp2 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.270+4108_270+4111d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | |||||||
chr16:74770374 | TTTTG | T | 4 | a0001c0003t0005g0361 a0001c0003t0005g0362 a0001c0003t0005g0363 others(1): Show |
4 | HG02257.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+4108_270+4111d others(6): Show |
FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770374 | |||||||
chr16:74770441 | G | A | 1 | a0002c0009t0012g0094 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.270+4045C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770441 | |||||||
chr16:74770510 | C | T | 4 | a0001c0001t0001g0218 a0001c0001t0002g0217 a0001c0001t0002g0219 others(1): Show |
4 | HG01071.hp1 HG01109.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+3976G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770510 | |||||||
chr16:74770881 | C | T | 2 | a0001c0002t0001g0100 a0001c0002t0001g0104 |
2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.270+3605G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770881 | |||||||
chr16:74770889 | C | T | 4 | a0001c0003t0002g0357 a0001c0003t0003g0355 a0001c0003t0005g0354 others(1): Show |
4 | HG02717.hp1 HG03486.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+3597G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770889 | |||||||
chr16:74770951 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.270+3535G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74770951 | |||||||
chr16:74771121 | A | G | 9 | a0001c0003t0005g0361 a0001c0003t0005g0362 a0001c0003t0005g0363 others(6): Show |
10 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+3365T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771121 | |||||||
chr16:74771230 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.270+3256T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771230 | |||||||
chr16:74771374 | A | G | 2 | a0001c0002t0001g0005 a0001c0002t0001g0101 |
3 | NA19066.hp1 NA19079.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.270+3112T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771374 | |||||||
chr16:74771626 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.270+2860C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771626 | |||||||
chr16:74771683 | A | G | 1 | a0002c0020t0017g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.270+2803T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771683 | |||||||
chr16:74771732 | C | G | 76 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(73): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+2754G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771732 | |||||||
chr16:74771770 | G | A | 76 | a0001c0001t0003g0197 a0001c0001t0003g0212 a0001c0001t0003g0213 others(73): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.270+2716C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771770 | |||||||
chr16:74771778 | C | T | 1 | a0001c0008t0003g0351 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.270+2708G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771778 | |||||||
chr16:74771790 | C | T | 34 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(31): Show |
36 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.270+2696G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771790 | |||||||
chr16:74771952 | CT | C | 48 | a0001c0001t0001g0026 a0001c0001t0001g0097 a0001c0001t0001g0099 others(45): Show |
50 | HG00099.hp1 HG00099.hp2 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.270+2533delA | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74771952 | |||||||
chr16:74772012 | G | A | 10 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(7): Show |
10 | HG00544.hp2 HG00597.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.270+2474C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772012 | |||||||
chr16:74772043 | C | T | 1 | a0001c0019t0016g0359 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270+2443G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772043 | |||||||
chr16:74772146 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18963.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.270+2340G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772146 | |||||||
chr16:74772231 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.270+2255C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772231 | |||||||
chr16:74772337 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.270+2149T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772337 | |||||||
chr16:74772345 | C | G | 32 | a0001c0001t0003g0212 a0001c0001t0003g0213 a0001c0001t0003g0214 others(29): Show |
33 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.270+2141G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772345 | |||||||
chr16:74772346 | T | C | 1 | a0001c0004t0004g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.270+2140A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772346 | |||||||
chr16:74772360 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.270+2126G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772360 | |||||||
chr16:74772375 | C | G | 2 | a0001c0003t0005g0298 a0001c0004t0004g0205 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.270+2111G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772375 | |||||||
chr16:74772386 | T | C | 1 | a0001c0001t0018g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.270+2100A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772386 | |||||||
chr16:74772406 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+2080A>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772406 | |||||||
chr16:74772470 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0023 others(216): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.270+2016G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772470 | |||||||
chr16:74772528 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02165.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.270+1958G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772528 | |||||||
chr16:74772721 | T | G | 1 | a0001c0001t0001g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.270+1765A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772721 | |||||||
chr16:74772794 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.270+1692T>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772794 | |||||||
chr16:74772871 | T | C | 2 | a0001c0002t0001g0269 a0001c0002t0006g0268 |
2 | HG02056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.270+1615A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74772871 | |||||||
chr16:74773000 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.270+1486G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773000 | |||||||
chr16:74773110 | G | C | 1 | a0001c0003t0002g0357 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.270+1376C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773110 | |||||||
chr16:74773114 | G | A | 1 | a0001c0001t0003g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.270+1372C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773114 | |||||||
chr16:74773127 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.270+1359G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773127 | |||||||
chr16:74773165 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0218 a0001c0001t0001g0222 others(167): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.270+1321A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773165 | |||||||
chr16:74773241 | A | C | 3 | a0001c0001t0003g0271 a0001c0005t0001g0358 a0001c0005t0013g0018 |
4 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+1245T>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773241 | |||||||
chr16:74773315 | C | A | 9 | a0001c0003t0001g0321 a0001c0003t0002g0320 a0001c0003t0003g0317 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+1171G>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773315 | |||||||
chr16:74773351 | AG | A | 64 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0001g0225 others(61): Show |
66 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.270+1134delC | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773351 | |||||||
chr16:74773594 | C | T | 70 | a0001c0001t0003g0271 a0001c0003t0001g0301 a0001c0003t0001g0308 others(67): Show |
73 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.270+892G>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773594 | |||||||
chr16:74773635 | T | C | 1 | a0001c0001t0003g0270 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.270+851A>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773635 | |||||||
chr16:74773665 | C | G | 29 | a0001c0003t0001g0301 a0001c0003t0001g0308 a0001c0003t0001g0309 others(26): Show |
30 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.270+821G>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773665 | |||||||
chr16:74773679 | T | G | 3 | a0001c0001t0003g0271 a0001c0005t0001g0358 a0001c0005t0013g0018 |
4 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+807A>C | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773679 | |||||||
chr16:74773682 | G | C | 8 | a0001c0003t0005g0361 a0001c0003t0005g0362 a0001c0003t0005g0363 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+804C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773682 | |||||||
chr16:74773959 | G | A | 2 | a0001c0001t0001g0272 a0001c0001t0002g0273 |
2 | NA18943.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.270+527C>T | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74773959 | |||||||
chr16:74774089 | G | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0277 a0001c0001t0001g0278 others(24): Show |
32 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.270+397C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774089 | |||||||
chr16:74774143 | G | T | 1 | a0001c0002t0001g0021 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.270+343C>A | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774143 | |||||||
chr16:74774167 | G | C | 1 | a0001c0002t0003g0297 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.270+319C>G | FA2H | ENSG00000103089.9 | transcript | ENST00000219368.8 | protein_coding | 1/6 | chr16 | 74774167 |