Item | Value |
---|---|
geneid | 10617 |
ensemblid | ENSG00000124356.17 |
hgncid | 16950 |
symbol | STAMBP |
name | STAM binding protein |
refseq_nuc | NM_213622.4 |
refseq_prot | NP_998787.1 |
ensembl_nuc | ENST00000394070.7 |
ensembl_prot | ENSP00000377633.2 |
mane_status | MANE Select |
chr | chr2 |
start | 73828961 |
end | 73867168 |
strand | + |
ver | v1.2 |
region | chr2:73828961-73867168 |
region5000 | chr2:73823961-73872168 |
regionname0 | STAMBP_chr2_73828961_73867168 |
regionname5000 | STAMBP_chr2_73823961_73872168 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 424 | 364 | 93 | 70 | 153 | 14 | 32 | 126 | STAMBP_chr2_73823961_73872168 | STAMBP | MSDHG others(419): Show |
chr2 | 73823961 | 73872168 |
a0002 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | MSDHG others(419): Show |
chr2 | 73823961 | 73872168 |
a0003 | 0/0 | 424 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | MSDHG others(419): Show |
chr2 | 73823961 | 73872168 |
a0004 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | MSDHG others(419): Show |
chr2 | 73823961 | 73872168 |
a0005 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | MSDHG others(419): Show |
chr2 | 73823961 | 73872168 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1272 | 308 | 61 | 62 | 138 | 14 | 31 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0001c0002 | 0/0 | 1272 | 49 | 31 | 7 | 11 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0001c0003 | 0/0 | 1272 | 6 | 0 | 1 | 4 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0001c0005 | 0/0 | 1272 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0002c0004 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0003c0007 | 0/0 | 1272 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0004c0008 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 | ||
a0005c0006 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | ATGTC others(1267): Show |
chr2 | 73823961 | 73872168 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 6746 | 129 | 20 | 23 | 64 | 8 | 12 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0002 | 0/0 | 6745 | 72 | 12 | 2 | 53 | 1 | 4 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0003 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0004 | 0/0 | 6745 | 19 | 0 | 13 | 2 | 1 | 3 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0005 | 0/0 | 6745 | 3 | 2 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0006 | 0/0 | 6745 | 3 | 3 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0007 | 0/0 | 6746 | 9 | 0 | 1 | 7 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0008 | 0/0 | 6746 | 8 | 6 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0011 | 0/0 | 6746 | 5 | 0 | 1 | 0 | 3 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0012 | 0/0 | 6745 | 5 | 0 | 0 | 4 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0013 | 0/0 | 6745 | 5 | 0 | 1 | 0 | 1 | 3 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0014 | 0/0 | 6745 | 4 | 1 | 3 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0015 | 0/0 | 6746 | 4 | 1 | 1 | 0 | 0 | 2 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0016 | 0/0 | 6745 | 4 | 0 | 3 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0017 | 0/0 | 6747 | 3 | 0 | 3 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6742): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0018 | 0/0 | 6745 | 3 | 3 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0019 | 0/0 | 6745 | 2 | 1 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0020 | 0/0 | 6746 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0021 | 0/0 | 6746 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0022 | 0/0 | 6745 | 2 | 2 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0023 | 0/0 | 6746 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0027 | 0/0 | 6746 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0028 | 0/0 | 6745 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0029 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0030 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0031 | 0/0 | 6746 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0032 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0033 | 0/0 | 6746 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0034 | 0/0 | 6746 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0035 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0036 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0037 | 0/0 | 6746 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0038 | 0/0 | 6745 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0039 | 0/0 | 6746 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0040 | 0/0 | 6745 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0041 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0042 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0043 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0044 | 0/0 | 6746 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0045 | 0/0 | 6745 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0046 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0001t0047 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0003 | 0/0 | 6745 | 21 | 7 | 3 | 11 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0005 | 0/0 | 6745 | 11 | 8 | 3 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0006 | 0/0 | 6745 | 8 | 8 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0009 | 0/0 | 6745 | 7 | 7 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0024 | 0/0 | 6747 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6742): Show |
chr2 | 73823961 | 73872168 |
a0001c0002t0025 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0003t0010 | 0/0 | 6745 | 6 | 0 | 1 | 4 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0001c0005t0003 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0002c0004t0003 | 0/0 | 6745 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0003c0007t0026 | 0/0 | 6745 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6740): Show |
chr2 | 73823961 | 73872168 |
a0004c0008t0001 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
a0005c0006t0001 | 0/0 | 6746 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | GTTTC others(6741): Show |
chr2 | 73823961 | 73872168 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0011g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0011g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0011g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0011g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0012g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0012g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0012g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0013g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0013g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0013g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0013g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0013g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0014g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0014g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0014g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0015g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0016g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0016g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0016g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0017g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0017g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0017g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0018g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0018g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0019g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0019g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0020g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0021g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0022g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0023g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0023g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0027g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0028g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0029g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0030g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0031g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0032g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0033g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0034g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0035g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0036g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0037g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0038g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0039g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0040g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0041g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0042g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0043g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0044g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0045g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0046g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0001t0047g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0002 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0024g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0002t0025g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0003t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0001c0005t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0002c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0003c0007t0026g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0004c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
a0005c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0011 | g0022 | EUR | GBR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0259 | EUR | GBR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0321 | EUR | FIN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | FIN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00621 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0255 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00733 | hp2 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0041 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00735 | hp2 | a0001 | c0001 | t0008 | g0318 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00738 | hp2 | a0001 | c0001 | t0023 | g0297 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00741 | hp1 | a0001 | c0001 | t0013 | g0237 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01069 | hp1 | a0001 | c0001 | t0021 | g0013 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01071 | hp2 | a0001 | c0001 | t0021 | g0013 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01081 | hp2 | a0001 | c0001 | t0017 | g0150 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01099 | hp1 | a0001 | c0001 | t0011 | g0022 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0326 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01167 | hp1 | a0001 | c0002 | t0005 | g0071 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01192 | hp1 | a0001 | c0001 | t0023 | g0295 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01243 | hp1 | a0001 | c0001 | t0014 | g0026 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01243 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0031 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01256 | hp2 | a0001 | c0001 | t0016 | g0020 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01257 | hp2 | a0001 | c0001 | t0020 | g0003 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01258 | hp1 | a0001 | c0001 | t0016 | g0020 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01258 | hp2 | a0001 | c0001 | t0020 | g0003 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01261 | hp1 | a0001 | c0003 | t0010 | g0056 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01261 | hp2 | a0001 | c0001 | t0019 | g0029 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0246 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01361 | hp1 | a0001 | c0001 | t0008 | g0315 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01516 | hp1 | a0001 | c0001 | t0011 | g0322 | EUR | IBS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01884 | hp1 | a0001 | c0002 | t0009 | g0035 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01884 | hp2 | a0001 | c0002 | t0006 | g0042 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0330 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01943 | hp1 | a0001 | c0001 | t0017 | g0165 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01975 | hp2 | a0001 | c0001 | t0034 | g0012 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01981 | hp1 | a0001 | c0001 | t0016 | g0258 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG01981 | hp2 | a0001 | c0001 | t0017 | g0011 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02040 | hp1 | a0001 | c0001 | t0012 | g0099 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0285 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0312 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0048 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02056 | hp2 | a0001 | c0001 | t0007 | g0242 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02071 | hp1 | a0002 | c0004 | t0003 | g0068 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0069 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02135 | hp2 | a0001 | c0001 | t0012 | g0178 | EAS | KHV | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0177 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0059 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CDX | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02258 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02273 | hp2 | a0001 | c0002 | t0024 | g0063 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02280 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0033 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0272 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0317 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02451 | hp2 | a0001 | c0002 | t0005 | g0073 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02572 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02615 | hp1 | a0001 | c0001 | t0044 | g0331 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02615 | hp2 | a0001 | c0002 | t0006 | g0023 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02622 | hp1 | a0001 | c0001 | t0036 | g0213 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02622 | hp2 | a0001 | c0001 | t0027 | g0028 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02630 | hp1 | a0001 | c0002 | t0006 | g0045 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02647 | hp2 | a0001 | c0002 | t0009 | g0037 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02683 | hp2 | a0001 | c0001 | t0011 | g0320 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02698 | hp1 | a0001 | c0001 | t0015 | g0182 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0274 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0323 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02723 | hp1 | a0001 | c0001 | t0043 | g0305 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02723 | hp2 | a0001 | c0001 | t0019 | g0027 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02809 | hp2 | a0001 | c0002 | t0005 | g0075 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02818 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0046 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02895 | hp1 | a0001 | c0001 | t0018 | g0207 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02895 | hp2 | a0001 | c0001 | t0008 | g0319 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02896 | hp1 | a0001 | c0002 | t0009 | g0036 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0208 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02922 | hp2 | a0001 | c0001 | t0022 | g0209 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0328 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03017 | hp1 | a0001 | c0001 | t0033 | g0158 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03041 | hp2 | a0001 | c0002 | t0005 | g0074 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03130 | hp1 | a0001 | c0001 | t0018 | g0210 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03130 | hp2 | a0001 | c0002 | t0009 | g0038 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0325 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0051 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03195 | hp1 | a0001 | c0002 | t0009 | g0034 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03209 | hp1 | a0001 | c0002 | t0009 | g0040 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03209 | hp2 | a0001 | c0005 | t0003 | g0060 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03225 | hp2 | a0001 | c0001 | t0046 | g0030 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03453 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03486 | hp1 | a0001 | c0002 | t0005 | g0072 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03516 | hp2 | a0001 | c0002 | t0005 | g0070 | AFR | ESN | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0313 | AFR | GWD | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03669 | hp2 | a0001 | c0001 | t0031 | g0202 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03688 | hp1 | a0001 | c0001 | t0013 | g0260 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03704 | hp1 | a0001 | c0001 | t0015 | g0203 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0224 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03831 | hp1 | a0001 | c0001 | t0038 | g0121 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0232 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03834 | hp1 | a0001 | c0001 | t0039 | g0288 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0218 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04204 | hp2 | a0001 | c0001 | t0012 | g0329 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | STU | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18522 | hp1 | a0003 | c0007 | t0026 | g0316 | AFR | YRI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18522 | hp2 | a0001 | c0001 | t0041 | g0310 | AFR | YRI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18942 | hp1 | a0001 | c0001 | t0035 | g0015 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18949 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0306 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18960 | hp1 | a0001 | c0003 | t0010 | g0062 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18964 | hp2 | a0001 | c0001 | t0032 | g0139 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18966 | hp2 | a0004 | c0008 | t0001 | g0009 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18968 | hp1 | a0001 | c0001 | t0040 | g0287 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18972 | hp1 | a0001 | c0001 | t0012 | g0090 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18980 | hp2 | a0001 | c0001 | t0012 | g0091 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18981 | hp1 | a0005 | c0006 | t0001 | g0007 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18987 | hp1 | a0001 | c0001 | t0030 | g0137 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18997 | hp1 | a0001 | c0001 | t0028 | g0138 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18997 | hp2 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19001 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19009 | hp2 | a0001 | c0003 | t0010 | g0044 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19010 | hp1 | a0001 | c0003 | t0010 | g0055 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19012 | hp2 | a0001 | c0001 | t0029 | g0016 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19030 | hp1 | a0001 | c0001 | t0037 | g0332 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0314 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19043 | hp2 | a0001 | c0002 | t0025 | g0077 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19062 | hp2 | a0001 | c0001 | t0016 | g0250 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19072 | hp1 | a0001 | c0003 | t0010 | g0043 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19075 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19089 | hp2 | a0001 | c0001 | t0045 | g0228 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19240 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | YRI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | YRI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20129 | hp1 | a0001 | c0001 | t0042 | g0303 | AFR | ASW | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20129 | hp2 | a0001 | c0001 | t0022 | g0212 | AFR | ASW | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20752 | hp2 | a0001 | c0001 | t0013 | g0005 | EUR | TSI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | TSI | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | GIH | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20905 | hp2 | a0001 | c0003 | t0010 | g0053 | SAS | GIH | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0078 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG03471 | hp2 | a0001 | c0001 | t0047 | g0327 | AFR | MSL | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
HG06807 | hp2 | a0001 | c0002 | t0009 | g0039 | AFR | USA | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | USA | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | USA | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0087 | REF | REF | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0156 | REF | REF | STAMBP_chr2_73823961_73872168 | STAMBP | chr2 | 73823961 | 73872168 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73847435 | C | G | 1 | a0004 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.424C>G | p.Leu142Val | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/10 | 986/6746 | 424/1275 | 142/424 | chr2 | 73847435 | |||
chr2:73847476 | G | T | 1 | a0003 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.465G>T | p.Gln155His | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/10 | 1027/6746 | 465/1275 | 155/424 | chr2 | 73847476 | |||
chr2:73849462 | C | G | 1 | a0005 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.842C>G | p.Thr281Arg | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/10 | 1404/6746 | 842/1275 | 281/424 | chr2 | 73849462 | |||
chr2:73862215 | G | A | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1231G>A | p.Val411Met | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1793/6746 | 1231/1275 | 411/424 | chr2 | 73862215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73830868 | T | C | 4 | a0001c0002 a0001c0003 a0001c0005 others(1): Show |
57 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(54): Show |
synonymous_variant | LOW | c.12T>C | p.His4His | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/10 | 574/6746 | 12/1275 | 4/424 | chr2 | 73830868 | |||
chr2:73850399 | C | G | 1 | a0001c0005 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.891C>G | p.Thr297Thr | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/10 | 1453/6746 | 891/1275 | 297/424 | chr2 | 73850399 | |||
chr2:73850429 | G | T | 1 | a0001c0003 | 6 | HG01261.hp1 NA18960.hp1 NA19009.hp2 others(3): Show |
synonymous_variant | LOW | c.921G>T | p.Gly307Gly | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/10 | 1483/6746 | 921/1275 | 307/424 | chr2 | 73850429 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73828978 | G | T | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-545G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | chr2 | 73828978 | |||||||
chr2:73829050 | C | G | 1 | a0001c0003t0010 | 6 | HG01261.hp1 NA18960.hp1 NA19009.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-473C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1807 | chr2 | 73829050 | ||||||
chr2:73829122 | C | T | 1 | a0001c0001t0046 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-401C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1735 | chr2 | 73829122 | ||||||
chr2:73829186 | G | C | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(17): Show |
87 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
5_prime_UTR_variant | MODIFIER | c.-337G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1671 | chr2 | 73829186 | ||||||
chr2:73829209 | A | G | 1 | a0001c0001t0023 | 2 | HG00738.hp2 HG01192.hp1 |
5_prime_UTR_variant | MODIFIER | c.-314A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1648 | chr2 | 73829209 | ||||||
chr2:73829257 | T | C | 1 | a0001c0001t0028 | 1 | NA18997.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-266T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | chr2 | 73829257 | |||||||
chr2:73829393 | C | G | 2 | a0001c0001t0008 a0001c0001t0011 |
13 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1464 | chr2 | 73829393 | ||||||
chr2:73829394 | C | G | 2 | a0001c0001t0014 a0001c0001t0046 |
5 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1463 | chr2 | 73829394 | ||||||
chr2:73829414 | C | T | 1 | a0001c0001t0013 | 5 | HG00741.hp1 HG02698.hp2 HG03688.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-109C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1443 | chr2 | 73829414 | ||||||
chr2:73829437 | A | G | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(30): Show |
205 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
5_prime_UTR_variant | MODIFIER | c.-86A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/10 | 1420 | chr2 | 73829437 | ||||||
chr2:73862934 | G | C | 1 | a0001c0001t0015 | 4 | HG00733.hp2 HG02145.hp1 HG02698.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 675 | chr2 | 73862934 | ||||||
chr2:73862936 | TA | T | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
206 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*685delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 685 | INFO_REALIGN_3_PRIME | chr2 | 73862936 | |||||
chr2:73863070 | G | A | 1 | a0001c0002t0025 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 811 | chr2 | 73863070 | ||||||
chr2:73863155 | G | A | 1 | a0003c0007t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 896 | chr2 | 73863155 | ||||||
chr2:73863274 | A | G | 1 | a0001c0001t0035 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1015 | chr2 | 73863274 | ||||||
chr2:73863363 | A | G | 1 | a0001c0001t0045 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1104A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1104 | chr2 | 73863363 | ||||||
chr2:73863376 | C | T | 3 | a0001c0001t0008 a0001c0001t0027 a0001c0001t0044 |
10 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1117C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1117 | chr2 | 73863376 | ||||||
chr2:73863691 | G | A | 1 | a0001c0001t0029 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1432G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1432 | chr2 | 73863691 | ||||||
chr2:73863735 | G | A | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0019 others(3): Show |
19 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1476G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1476 | chr2 | 73863735 | ||||||
chr2:73863817 | G | T | 1 | a0001c0001t0013 | 5 | HG00741.hp1 HG02698.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1558G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1558 | chr2 | 73863817 | ||||||
chr2:73863846 | C | CT | 2 | a0001c0001t0017 a0001c0002t0024 |
4 | HG01081.hp2 HG01943.hp1 HG01981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1590dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1591 | INFO_REALIGN_3_PRIME | chr2 | 73863846 | |||||
chr2:73863935 | C | G | 1 | a0001c0001t0034 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1676C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1676 | chr2 | 73863935 | ||||||
chr2:73863970 | T | C | 12 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(9): Show |
51 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1711T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1711 | chr2 | 73863970 | ||||||
chr2:73864028 | T | C | 1 | a0001c0001t0040 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1769 | chr2 | 73864028 | ||||||
chr2:73864200 | T | C | 38 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(35): Show |
208 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*1941T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 1941 | chr2 | 73864200 | ||||||
chr2:73864340 | C | G | 1 | a0001c0001t0033 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2081C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2081 | chr2 | 73864340 | ||||||
chr2:73864354 | T | C | 1 | a0001c0001t0031 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2095T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2095 | chr2 | 73864354 | ||||||
chr2:73864456 | G | C | 1 | a0001c0001t0008 | 8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2197G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2197 | chr2 | 73864456 | ||||||
chr2:73864523 | G | A | 7 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0020 others(4): Show |
36 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2264G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2264 | chr2 | 73864523 | ||||||
chr2:73864532 | G | A | 1 | a0001c0001t0038 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2273G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2273 | chr2 | 73864532 | ||||||
chr2:73864547 | T | G | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0027 others(2): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2288T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2288 | chr2 | 73864547 | ||||||
chr2:73864598 | A | G | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0027 others(2): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2339A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2339 | chr2 | 73864598 | ||||||
chr2:73864678 | C | T | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(33): Show |
206 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2419 | chr2 | 73864678 | ||||||
chr2:73864893 | T | C | 1 | a0001c0001t0041 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2634T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2634 | chr2 | 73864893 | ||||||
chr2:73864976 | C | A | 1 | a0001c0002t0025 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2717C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2717 | chr2 | 73864976 | ||||||
chr2:73864989 | T | C | 1 | a0001c0001t0019 | 2 | HG01261.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2730T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2730 | chr2 | 73864989 | ||||||
chr2:73864992 | C | T | 19 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(16): Show |
79 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2733C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2733 | chr2 | 73864992 | ||||||
chr2:73864993 | A | G | 1 | a0001c0001t0022 | 2 | HG02922.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2734A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2734 | chr2 | 73864993 | ||||||
chr2:73865029 | A | G | 1 | a0001c0001t0036 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2770A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2770 | chr2 | 73865029 | ||||||
chr2:73865049 | T | G | 1 | a0001c0001t0011 | 5 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2790T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2790 | chr2 | 73865049 | ||||||
chr2:73865102 | G | T | 1 | a0001c0001t0022 | 2 | HG02922.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2843G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2843 | chr2 | 73865102 | ||||||
chr2:73865212 | C | T | 1 | a0001c0001t0021 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2953C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 2953 | chr2 | 73865212 | ||||||
chr2:73865581 | A | G | 1 | a0001c0001t0036 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3322A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3322 | chr2 | 73865581 | ||||||
chr2:73865618 | C | G | 1 | a0001c0001t0043 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3359C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3359 | chr2 | 73865618 | ||||||
chr2:73865702 | G | A | 6 | a0001c0001t0003 a0001c0001t0016 a0001c0002t0003 others(3): Show |
34 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3443G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3443 | chr2 | 73865702 | ||||||
chr2:73865717 | C | G | 2 | a0001c0001t0011 a0001c0001t0037 |
6 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3458C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3458 | chr2 | 73865717 | ||||||
chr2:73865758 | T | C | 1 | a0003c0007t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3499T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3499 | chr2 | 73865758 | ||||||
chr2:73865800 | G | GC | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0027 others(2): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3544dupC | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3545 | INFO_REALIGN_3_PRIME | chr2 | 73865800 | |||||
chr2:73865836 | G | C | 1 | a0001c0001t0032 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3577G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3577 | chr2 | 73865836 | ||||||
chr2:73866047 | G | A | 1 | a0001c0001t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3788G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3788 | chr2 | 73866047 | ||||||
chr2:73866239 | C | T | 1 | a0003c0007t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 3980 | chr2 | 73866239 | ||||||
chr2:73866503 | G | A | 1 | a0001c0001t0039 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4244G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4244 | chr2 | 73866503 | ||||||
chr2:73866513 | C | T | 1 | a0001c0001t0023 | 2 | HG00738.hp2 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4254C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4254 | chr2 | 73866513 | ||||||
chr2:73866525 | T | C | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(20): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*4266T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4266 | chr2 | 73866525 | ||||||
chr2:73866555 | T | A | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(20): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*4296T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4296 | chr2 | 73866555 | ||||||
chr2:73866674 | C | T | 1 | a0001c0001t0042 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4415C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4415 | chr2 | 73866674 | ||||||
chr2:73866706 | G | T | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0027 others(2): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4447G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 10/10 | 4447 | chr2 | 73866706 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73829627 | A | C | 2 | a0001c0001t0037g0332 a0001c0001t0044g0331 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-13+117A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73829627 | |||||||
chr2:73829663 | G | A | 1 | a0001c0002t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+153G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73829663 | |||||||
chr2:73829962 | T | C | 10 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0014g0026 others(7): Show |
10 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+452T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73829962 | |||||||
chr2:73829969 | T | A | 49 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(46): Show |
57 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.-13+459T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73829969 | |||||||
chr2:73829988 | A | G | 1 | a0001c0002t0003g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-13+478A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73829988 | |||||||
chr2:73830337 | G | T | 1 | a0001c0001t0005g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-12-508G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830337 | |||||||
chr2:73830474 | A | C | 9 | a0001c0002t0005g0002 a0001c0002t0005g0070 a0001c0002t0005g0071 others(6): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12-371A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830474 | |||||||
chr2:73830569 | C | T | 4 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(1): Show |
4 | HG00741.hp2 HG01256.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-276C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830569 | |||||||
chr2:73830686 | C | T | 1 | a0001c0001t0012g0329 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-12-159C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830686 | |||||||
chr2:73830738 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0079 a0001c0001t0002g0080 |
4 | HG02165.hp1 NA18988.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-107G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830738 | |||||||
chr2:73830813 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-12-32G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 1/9 | chr2 | 73830813 | |||||||
chr2:73831247 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18978.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.203+188G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831247 | |||||||
chr2:73831375 | A | G | 29 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(26): Show |
30 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.203+316A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831375 | |||||||
chr2:73831387 | C | T | 32 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(29): Show |
37 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.203+328C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831387 | |||||||
chr2:73831693 | T | C | 1 | a0001c0002t0003g0041 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.203+634T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831693 | |||||||
chr2:73831767 | G | T | 197 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(194): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.203+708G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831767 | |||||||
chr2:73831841 | A | C | 1 | a0001c0001t0008g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.203+782A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831841 | |||||||
chr2:73831986 | A | G | 1 | a0001c0001t0015g0203 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.203+927A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73831986 | |||||||
chr2:73832084 | C | CAT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0189 a0001c0001t0001g0190 others(15): Show |
19 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.203+1049_203+1050d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832084 | ||||||
chr2:73832084 | C | CATAT | 4 | a0001c0001t0031g0202 a0001c0002t0009g0038 a0001c0002t0009g0039 others(1): Show |
4 | HG03130.hp2 HG03209.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1047_203+1050d others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832084 | ||||||
chr2:73832084 | C | G | 5 | a0001c0002t0003g0065 a0001c0002t0003g0066 a0001c0002t0003g0067 others(2): Show |
5 | HG00438.hp2 HG00621.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1025C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832084 | |||||||
chr2:73832084 | C | T | 9 | a0001c0002t0005g0002 a0001c0002t0005g0070 a0001c0002t0005g0071 others(6): Show |
12 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.203+1025C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832084 | |||||||
chr2:73832084 | CAT | C | 7 | a0001c0001t0001g0085 a0001c0001t0002g0204 a0001c0001t0002g0205 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+1049_203+1050d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832084 | ||||||
chr2:73832106 | T | TACAC | 4 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(1): Show |
4 | HG01361.hp1 HG02055.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1048_203+1049i others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832106 | ||||||
chr2:73832108 | T | C | 9 | a0001c0001t0001g0084 a0001c0001t0002g0204 a0001c0001t0002g0205 others(6): Show |
9 | HG01361.hp1 HG02055.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+1049T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832108 | |||||||
chr2:73832108 | T | TACACAC | 4 | a0001c0001t0008g0317 a0001c0001t0008g0318 a0001c0001t0008g0319 others(1): Show |
4 | HG00735.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1054_203+1055i others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TACACACA others(3): Show |
1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.203+1054_203+1055i others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATACA others(3): Show |
1 | a0001c0001t0011g0022 | 2 | HG00099.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.203+1050_203+1051i others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(5): Show |
1 | a0001c0001t0011g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.203+1050_203+1051i others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(7): Show |
1 | a0001c0001t0006g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(5): Show |
6 | a0001c0002t0005g0002 a0001c0002t0005g0071 a0001c0002t0005g0072 others(3): Show |
9 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(9): Show |
1 | a0001c0001t0046g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(11): Show |
1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(7): Show |
2 | a0001c0002t0005g0076 a0001c0002t0006g0042 |
2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.203+1050_203+1051i others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(9): Show |
13 | a0001c0001t0002g0019 a0001c0001t0002g0215 a0001c0001t0002g0216 others(10): Show |
14 | HG03704.hp2 HG04204.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(11): Show |
1 | a0001c0001t0002g0214 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(11): Show |
39 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0079 others(36): Show |
45 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(13): Show |
4 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0016g0020 others(1): Show |
5 | HG00423.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(15): Show |
8 | a0001c0001t0005g0325 a0001c0001t0005g0326 a0001c0001t0006g0024 others(5): Show |
8 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(13): Show |
12 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0264 others(9): Show |
12 | HG00140.hp2 HG01981.hp1 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(15): Show |
1 | a0001c0001t0002g0257 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.203+1050_203+1051i others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(17): Show |
2 | a0001c0001t0014g0033 a0001c0001t0019g0027 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.203+1050_203+1051i others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(15): Show |
20 | a0001c0001t0002g0273 a0001c0001t0002g0275 a0001c0001t0002g0276 others(17): Show |
20 | HG00544.hp1 HG01069.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(17): Show |
4 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0002t0003g0047 others(1): Show |
4 | HG01074.hp2 HG02055.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(19): Show |
3 | a0001c0001t0005g0330 a0001c0001t0019g0029 a0001c0001t0027g0028 |
3 | HG01261.hp2 HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.203+1050_203+1051i others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(17): Show |
16 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(13): Show |
19 | HG00438.hp2 HG00621.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(19): Show |
1 | a0001c0002t0003g0052 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(19): Show |
14 | a0001c0001t0002g0298 a0001c0001t0002g0299 a0001c0001t0002g0300 others(11): Show |
14 | HG00735.hp1 HG00738.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(21): Show |
7 | a0001c0001t0002g0307 a0001c0001t0002g0309 a0001c0001t0007g0306 others(4): Show |
7 | HG02135.hp1 HG02723.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(30): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(23): Show |
4 | a0001c0001t0002g0081 a0001c0001t0041g0310 a0001c0002t0003g0061 others(1): Show |
4 | NA18522.hp2 NA18960.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1050_203+1051i others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(25): Show |
2 | a0001c0002t0003g0064 a0001c0002t0024g0063 |
2 | HG02273.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.203+1050_203+1051i others(34): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832108 | T | TATATATA others(33): Show |
1 | a0001c0001t0002g0311 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.203+1050_203+1051i others(42): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832108 | ||||||
chr2:73832229 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(36): Show |
43 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.203+1170C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832229 | |||||||
chr2:73832385 | G | T | 1 | a0001c0002t0005g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.203+1326G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832385 | |||||||
chr2:73832460 | C | CA | 43 | a0001c0001t0001g0168 a0001c0001t0002g0081 a0001c0002t0003g0001 others(40): Show |
51 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.203+1417dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832460 | ||||||
chr2:73832460 | CA | C | 9 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0188 others(6): Show |
9 | HG03195.hp2 NA18957.hp2 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.203+1417delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73832460 | ||||||
chr2:73832462 | A | G | 12 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.203+1403A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832462 | |||||||
chr2:73832477 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.203+1418G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832477 | |||||||
chr2:73832628 | C | T | 1 | a0001c0002t0025g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+1569C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832628 | |||||||
chr2:73832764 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0035g0015 |
2 | NA18942.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.203+1705C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73832764 | |||||||
chr2:73833038 | G | A | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203+1979G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833038 | |||||||
chr2:73833042 | A | C | 1 | a0001c0001t0002g0080 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.203+1983A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833042 | |||||||
chr2:73833164 | C | G | 1 | a0001c0003t0010g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.203+2105C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833164 | |||||||
chr2:73833169 | T | G | 16 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.203+2110T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833169 | |||||||
chr2:73833404 | AAATTAT | A | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.203+2353_203+2358d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73833404 | ||||||
chr2:73833513 | T | TACTGC | 41 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(38): Show |
49 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.203+2454_203+2455i others(7): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833513 | |||||||
chr2:73833583 | G | T | 1 | a0001c0001t0017g0165 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.203+2524G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833583 | |||||||
chr2:73833977 | G | A | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.203+2918G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73833977 | |||||||
chr2:73834080 | G | A | 1 | a0001c0001t0045g0228 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.203+3021G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834080 | |||||||
chr2:73834105 | G | A | 41 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(38): Show |
49 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.203+3046G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834105 | |||||||
chr2:73834209 | TAAAAAAA others(3): Show |
T | 1 | a0001c0002t0009g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203+3169_203+3178d others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834209 | ||||||
chr2:73834218 | AAAAAAAA others(19): Show |
A | 2 | a0001c0002t0006g0045 a0001c0002t0006g0046 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.203+3161_203+3186d others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834218 | ||||||
chr2:73834218 | AAAAAAAA others(23): Show |
A | 1 | a0001c0002t0006g0059 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.203+3161_203+3190d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834218 | ||||||
chr2:73834219 | AAAAAAAA others(20): Show |
A | 1 | a0001c0002t0006g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.203+3162_203+3188d others(29): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834219 | ||||||
chr2:73834219 | AAAAAAAA others(28): Show |
A | 1 | a0001c0003t0010g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.203+3162_203+3196d others(37): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834219 | ||||||
chr2:73834220 | AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0011g0320 a0001c0003t0010g0056 |
2 | HG01261.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.203+3163_203+3184d others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834220 | ||||||
chr2:73834220 | AAAAAAAA others(19): Show |
A | 1 | a0001c0003t0010g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.203+3163_203+3188d others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834220 | ||||||
chr2:73834220 | AAAAAAAA others(21): Show |
A | 1 | a0001c0002t0003g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.203+3163_203+3190d others(30): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834220 | ||||||
chr2:73834220 | AAAAAAAA others(23): Show |
A | 4 | a0001c0002t0003g0061 a0001c0002t0006g0006 a0001c0002t0006g0042 others(1): Show |
5 | HG01884.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+3163_203+3192d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834220 | ||||||
chr2:73834221 | AAAAAAAA others(22): Show |
A | 1 | a0001c0002t0003g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.203+3164_203+3192d others(31): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834221 | ||||||
chr2:73834222 | AAAAAAAA others(15): Show |
A | 2 | a0001c0001t0011g0022 a0001c0001t0011g0322 |
3 | HG00099.hp1 HG01099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.203+3165_203+3186d others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834222 | ||||||
chr2:73834222 | AAAAAAAA others(17): Show |
A | 4 | a0001c0001t0011g0321 a0001c0003t0010g0043 a0001c0003t0010g0044 others(1): Show |
4 | HG00323.hp1 NA19009.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+3165_203+3188d others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834222 | ||||||
chr2:73834222 | AAAAAAAA others(23): Show |
A | 3 | a0001c0002t0003g0050 a0001c0002t0003g0057 a0001c0002t0003g0064 |
3 | NA19001.hp1 NA19003.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.203+3165_203+3194d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834222 | ||||||
chr2:73834222 | AAAAAAAA others(25): Show |
A | 9 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0058 others(6): Show |
12 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.203+3165_203+3196d others(34): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834222 | ||||||
chr2:73834223 | AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203+3166_203+3192d others(29): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834223 | ||||||
chr2:73834223 | AAAAAAAA others(22): Show |
A | 1 | a0001c0002t0003g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.203+3166_203+3194d others(31): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834223 | ||||||
chr2:73834223 | AAAAAAAA others(40): Show |
A | 1 | a0001c0001t0014g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.203+3166_203+3212d others(49): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834223 | ||||||
chr2:73834224 | AAAAAAAA others(21): Show |
A | 1 | a0001c0002t0003g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.203+3167_203+3194d others(30): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834224 | ||||||
chr2:73834224 | AAAAAAAA others(23): Show |
A | 3 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0052 |
3 | HG02055.hp2 NA19083.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.203+3167_203+3196d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834224 | ||||||
chr2:73834225 | AAAAAAAA others(16): Show |
A | 3 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 |
3 | HG00741.hp2 HG01256.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.203+3168_203+3190d others(25): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834225 | ||||||
chr2:73834225 | AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0027g0028 a0001c0001t0046g0030 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.203+3168_203+3192d others(27): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834225 | ||||||
chr2:73834225 | AAAAAAAA others(36): Show |
A | 2 | a0001c0002t0005g0002 a0001c0002t0005g0072 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.203+3168_203+3210d others(45): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834225 | ||||||
chr2:73834226 | AAAAAAAA others(21): Show |
A | 2 | a0001c0001t0019g0027 a0001c0001t0019g0029 |
2 | HG01261.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.203+3169_203+3196d others(30): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834226 | ||||||
chr2:73834226 | AAAAAAAA others(37): Show |
A | 2 | a0001c0002t0005g0073 a0001c0002t0005g0075 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.203+3169_203+3212d others(46): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834226 | ||||||
chr2:73834227 | AAAAAAAA others(36): Show |
A | 4 | a0001c0002t0005g0002 a0001c0002t0005g0071 a0001c0002t0005g0074 others(1): Show |
6 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+3170_203+3212d others(45): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834227 | ||||||
chr2:73834228 | AAAAAAAA others(5): Show |
A | 1 | a0001c0002t0005g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.203+3171_203+3182d others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834228 | ||||||
chr2:73834228 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0192 a0001c0001t0008g0312 |
2 | HG01928.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.203+3171_203+3188d others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834228 | ||||||
chr2:73834228 | AAAAAAAA others(13): Show |
A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
7 | HG00423.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+3171_203+3190d others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834228 | ||||||
chr2:73834228 | AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.203+3171_203+3198d others(30): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834228 | ||||||
chr2:73834228 | AAAAAAAA others(23): Show |
A | 1 | a0001c0001t0002g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203+3171_203+3200d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834228 | ||||||
chr2:73834229 | AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0008g0313 a0001c0002t0006g0023 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.203+3172_203+3182d others(13): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834229 | ||||||
chr2:73834229 | AAAAAAAA others(6): Show |
A | 1 | a0001c0002t0025g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+3172_203+3184d others(15): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834229 | ||||||
chr2:73834229 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0005g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.203+3172_203+3200d others(31): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834229 | ||||||
chr2:73834230 | A | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0293 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.203+3171A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834230 | |||||||
chr2:73834230 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0008g0318 a0001c0001t0008g0328 |
2 | HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.203+3173_203+3190d others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834230 | ||||||
chr2:73834230 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0146 a0001c0001t0008g0317 |
2 | HG00642.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.203+3173_203+3192d others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834230 | ||||||
chr2:73834230 | AAAAAAAA others(23): Show |
A | 1 | a0001c0001t0047g0327 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.203+3173_203+3202d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834230 | ||||||
chr2:73834231 | AAAAAAAT others(22): Show |
A | 2 | a0001c0001t0005g0325 a0001c0001t0005g0326 |
2 | HG01099.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.203+3174_203+3202d others(31): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834231 | ||||||
chr2:73834231 | AAAAAAAT others(28): Show |
A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0200 |
3 | NA18956.hp1 NA19089.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.203+3174_203+3208d others(37): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834231 | ||||||
chr2:73834232 | A | T | 4 | a0001c0001t0002g0206 a0001c0001t0002g0252 a0001c0001t0002g0253 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+3173A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834232 | |||||||
chr2:73834232 | AAAAAATA others(3): Show |
A | 1 | a0001c0002t0009g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.203+3175_203+3184d others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834232 | ||||||
chr2:73834232 | AAAAAATA others(23): Show |
A | 1 | a0001c0001t0006g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.203+3175_203+3204d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834232 | ||||||
chr2:73834233 | AAAAATAT others(6): Show |
A | 1 | a0001c0001t0008g0314 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.203+3176_203+3188d others(15): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834233 | ||||||
chr2:73834233 | AAAAATAT others(20): Show |
A | 1 | a0001c0001t0042g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.203+3176_203+3202d others(29): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834233 | ||||||
chr2:73834233 | AAAAATAT others(28): Show |
A | 1 | a0001c0001t0001g0184 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.203+3176_203+3210d others(37): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834233 | ||||||
chr2:73834234 | A | T | 5 | a0001c0001t0002g0206 a0001c0001t0002g0252 a0001c0001t0002g0253 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+3175A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834234 | |||||||
chr2:73834234 | AAAATATA others(3): Show |
A | 3 | a0001c0002t0009g0034 a0001c0002t0009g0038 a0001c0002t0009g0039 |
3 | HG03130.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.203+3177_203+3186d others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834234 | ||||||
chr2:73834234 | AAAATATA others(7): Show |
A | 2 | a0001c0001t0002g0286 a0001c0001t0008g0315 |
2 | HG01361.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.203+3177_203+3190d others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834234 | ||||||
chr2:73834235 | AAATATAT others(4): Show |
A | 2 | a0001c0001t0001g0153 a0001c0001t0002g0271 |
2 | HG01074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.203+3178_203+3188d others(13): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834235 | ||||||
chr2:73834235 | AAATATAT others(6): Show |
A | 1 | a0001c0001t0002g0211 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.203+3178_203+3190d others(15): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834235 | ||||||
chr2:73834236 | A | AAAAAAAT others(10): Show |
1 | a0001c0001t0018g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.203+3178_203+3179i others(19): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | A | AAAAAATA others(3): Show |
1 | a0001c0001t0044g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.203+3178_203+3179i others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | A | AAAAAATA others(9): Show |
1 | a0001c0001t0018g0208 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.203+3178_203+3179i others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | A | T | 6 | a0001c0001t0002g0206 a0001c0001t0002g0252 a0001c0001t0002g0253 others(3): Show |
6 | HG02818.hp1 HG03041.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+3177A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834236 | |||||||
chr2:73834236 | AATATAT | A | 13 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0104 others(10): Show |
13 | HG00621.hp2 HG00738.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.203+3223_203+3228d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(1): Show |
A | 14 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(11): Show |
14 | HG00323.hp2 HG00597.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+3221_203+3228d others(10): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(3): Show |
A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(22): Show |
27 | HG01074.hp1 HG01167.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.203+3219_203+3228d others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(5): Show |
A | 11 | a0001c0001t0001g0012 a0001c0001t0002g0216 a0001c0001t0002g0230 others(8): Show |
11 | HG01168.hp1 HG01257.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.203+3217_203+3228d others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(7): Show |
A | 34 | a0001c0001t0002g0219 a0001c0001t0002g0223 a0001c0001t0002g0226 others(31): Show |
36 | HG00423.hp1 HG00733.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.203+3215_203+3228d others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(9): Show |
A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0220 a0001c0001t0002g0290 others(2): Show |
6 | HG01109.hp2 HG02922.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+3213_203+3228d others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.203+3211_203+3228d others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(15): Show |
A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG00544.hp2 HG00642.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+3207_203+3228d others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(17): Show |
A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0085 others(12): Show |
18 | HG00639.hp1 HG00733.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.203+3205_203+3228d others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(19): Show |
A | 1 | a0001c0001t0002g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.203+3203_203+3228d others(28): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834236 | AATATATA others(23): Show |
A | 1 | a0001c0001t0018g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.203+3199_203+3228d others(32): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73834236 | ||||||
chr2:73834237 | ATATAT | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0103 others(4): Show |
7 | HG01515.hp1 HG02970.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+3179_203+3183d others(7): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT | A | 9 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0095 others(6): Show |
9 | HG00639.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.203+3179_203+3185d others(9): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(2): Show |
A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0114 a0001c0001t0001g0116 others(17): Show |
20 | HG00099.hp2 HG01070.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.203+3179_203+3187d others(11): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(4): Show |
A | 16 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(13): Show |
18 | HG00140.hp1 HG00738.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.203+3179_203+3189d others(13): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(6): Show |
A | 22 | a0001c0001t0002g0021 a0001c0001t0002g0080 a0001c0001t0002g0214 others(19): Show |
23 | HG00140.hp2 HG00597.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.203+3179_203+3191d others(15): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(8): Show |
A | 9 | a0001c0001t0002g0221 a0001c0001t0002g0248 a0001c0001t0002g0257 others(6): Show |
9 | HG00544.hp1 HG01070.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+3179_203+3193d others(17): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0041g0310 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.203+3179_203+3195d others(19): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0036g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.203+3179_203+3199d others(23): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(16): Show |
A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
17 | HG00438.hp1 HG02135.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.203+3179_203+3201d others(25): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0015g0203 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.203+3179_203+3203d others(27): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834237 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0031g0202 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.203+3179_203+3207d others(31): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834237 | |||||||
chr2:73834238 | T | A | 2 | a0001c0001t0001g0162 a0001c0001t0037g0332 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.203+3179T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834238 | |||||||
chr2:73834240 | T | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0162 |
3 | HG02717.hp1 NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.203+3181T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834240 | |||||||
chr2:73834242 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0094 a0001c0001t0001g0112 others(2): Show |
6 | HG01192.hp2 HG01496.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.203+3183T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834242 | |||||||
chr2:73834244 | T | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0093 others(16): Show |
19 | HG00621.hp2 HG00738.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.203+3185T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834244 | |||||||
chr2:73834246 | T | A | 31 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(28): Show |
31 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.203+3187T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834246 | |||||||
chr2:73834248 | T | A | 56 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0018 others(53): Show |
58 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.203+3189T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834248 | |||||||
chr2:73834250 | T | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(37): Show |
42 | HG00140.hp1 HG00597.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.203+3191T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834250 | |||||||
chr2:73834252 | T | A | 52 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0140 others(49): Show |
55 | HG00140.hp2 HG00423.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.203+3193T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834252 | |||||||
chr2:73834254 | T | A | 28 | a0001c0001t0002g0019 a0001c0001t0002g0081 a0001c0001t0002g0220 others(25): Show |
30 | HG00140.hp2 HG00544.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.203+3195T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834254 | |||||||
chr2:73834256 | T | A | 5 | a0001c0001t0001g0143 a0001c0001t0002g0220 a0001c0001t0004g0246 others(2): Show |
5 | HG01346.hp2 HG02886.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+3197T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834256 | |||||||
chr2:73834258 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.203+3199T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834258 | |||||||
chr2:73834260 | T | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0169 others(2): Show |
5 | HG00544.hp2 HG00642.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+3201T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834260 | |||||||
chr2:73834262 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(31): Show |
38 | HG00438.hp1 HG00544.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.203+3203T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834262 | |||||||
chr2:73834264 | T | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(23): Show |
30 | HG00544.hp2 HG00642.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.203+3205T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834264 | |||||||
chr2:73834266 | T | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
9 | HG01081.hp1 HG01106.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+3207T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834266 | |||||||
chr2:73834268 | T | A | 2 | a0001c0001t0018g0210 a0001c0001t0031g0202 |
2 | HG03130.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.203+3209T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834268 | |||||||
chr2:73834270 | T | A | 2 | a0001c0001t0018g0210 a0001c0001t0031g0202 |
2 | HG03130.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.203+3211T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834270 | |||||||
chr2:73834272 | T | A | 2 | a0001c0001t0018g0210 a0001c0001t0031g0202 |
2 | HG03130.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.203+3213T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834272 | |||||||
chr2:73834274 | T | A | 1 | a0001c0001t0018g0210 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.203+3215T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834274 | |||||||
chr2:73834285 | A | G | 8 | a0001c0002t0006g0023 a0001c0002t0009g0034 a0001c0002t0009g0035 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.203+3226A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834285 | |||||||
chr2:73834290 | G | A | 70 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(67): Show |
79 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.203+3231G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834290 | |||||||
chr2:73834458 | A | C | 1 | a0001c0001t0002g0301 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.203+3399A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834458 | |||||||
chr2:73834590 | G | T | 1 | a0001c0001t0040g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.203+3531G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834590 | |||||||
chr2:73834938 | C | T | 1 | a0001c0002t0009g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.203+3879C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834938 | |||||||
chr2:73834995 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0175 a0001c0001t0001g0179 others(3): Show |
6 | HG00438.hp1 NA18943.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+3936T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73834995 | |||||||
chr2:73835079 | G | T | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.203+4020G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835079 | |||||||
chr2:73835092 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
8 | HG00423.hp2 HG00642.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.203+4033G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835092 | |||||||
chr2:73835105 | G | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203+4046G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835105 | |||||||
chr2:73835123 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.203+4064C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835123 | |||||||
chr2:73835236 | C | G | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.203+4177C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835236 | |||||||
chr2:73835247 | G | A | 4 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(1): Show |
5 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+4188G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835247 | |||||||
chr2:73835295 | A | G | 7 | a0001c0002t0005g0002 a0001c0002t0005g0071 a0001c0002t0005g0072 others(4): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.203+4236A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835295 | |||||||
chr2:73835303 | A | G | 27 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(24): Show |
28 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.203+4244A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835303 | |||||||
chr2:73835340 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0001g0124 a0001c0001t0001g0142 others(7): Show |
10 | HG02717.hp1 NA18612.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.203+4281C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835340 | |||||||
chr2:73835353 | C | CA | 116 | a0001c0001t0001g0015 a0001c0001t0001g0084 a0001c0001t0001g0092 others(113): Show |
122 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.203+4312dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73835353 | ||||||
chr2:73835353 | CA | C | 8 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0163 others(5): Show |
8 | HG00140.hp1 HG00323.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.203+4312delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73835353 | ||||||
chr2:73835488 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0096 a0001c0001t0001g0106 others(2): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+4429T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835488 | |||||||
chr2:73835740 | T | C | 3 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0024g0063 |
6 | HG00735.hp1 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.203+4681T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835740 | |||||||
chr2:73835775 | A | G | 4 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(1): Show |
5 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+4716A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73835775 | |||||||
chr2:73836195 | T | C | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5136T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836195 | |||||||
chr2:73836196 | C | T | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5137C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836196 | |||||||
chr2:73836213 | C | T | 1 | a0001c0001t0037g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.203+5154C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836213 | |||||||
chr2:73836263 | G | A | 1 | a0001c0002t0003g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.203+5204G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836263 | |||||||
chr2:73836391 | C | A | 105 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(102): Show |
111 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.203+5332C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836391 | |||||||
chr2:73836417 | G | C | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5358G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836417 | |||||||
chr2:73836418 | C | G | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5359C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836418 | |||||||
chr2:73836546 | T | C | 196 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(193): Show |
211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.203+5487T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836546 | |||||||
chr2:73836885 | G | C | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5826G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836885 | |||||||
chr2:73836886 | C | G | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+5827C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836886 | |||||||
chr2:73836930 | C | T | 1 | a0001c0001t0044g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.203+5871C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73836930 | |||||||
chr2:73837001 | A | C | 1 | a0001c0001t0036g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.203+5942A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837001 | |||||||
chr2:73837306 | C | T | 2 | a0001c0002t0006g0006 a0001c0002t0006g0042 |
4 | HG01884.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+6247C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837306 | |||||||
chr2:73837308 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA19058.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.203+6249G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837308 | |||||||
chr2:73837337 | G | T | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+6278G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837337 | |||||||
chr2:73837367 | C | T | 1 | a0001c0002t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.203+6308C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837367 | |||||||
chr2:73837381 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG00438.hp1 HG02135.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.203+6322C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837381 | |||||||
chr2:73837429 | CA | C | 116 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(113): Show |
122 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.203+6376delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837429 | ||||||
chr2:73837449 | G | A | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | NA18952.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.203+6390G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837449 | |||||||
chr2:73837517 | G | A | 4 | a0001c0001t0005g0325 a0001c0001t0005g0326 a0001c0001t0005g0330 others(1): Show |
4 | HG01099.hp2 HG01891.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+6458G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837517 | |||||||
chr2:73837584 | C | CA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0082 a0001c0001t0001g0085 others(15): Show |
18 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.203+6553dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837584 | ||||||
chr2:73837584 | CA | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0096 a0001c0001t0001g0103 others(16): Show |
23 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.203+6553delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837584 | ||||||
chr2:73837584 | CAA | C | 68 | a0001c0001t0002g0081 a0001c0001t0002g0215 a0001c0001t0002g0266 others(65): Show |
74 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.203+6552_203+6553d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837584 | ||||||
chr2:73837584 | CAAA | C | 103 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(100): Show |
109 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.203+6551_203+6553d others(5): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837584 | ||||||
chr2:73837615 | AC | A | 5 | a0001c0002t0006g0006 a0001c0002t0006g0042 a0001c0002t0006g0045 others(2): Show |
7 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.203+6557delC | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837615 | |||||||
chr2:73837685 | T | C | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.203+6626T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837685 | |||||||
chr2:73837730 | TGTTCTGA others(5): Show |
T | 1 | a0001c0001t0007g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.203+6674_203+6685d others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73837730 | ||||||
chr2:73837992 | C | T | 133 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(130): Show |
139 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.204-6821C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73837992 | |||||||
chr2:73838471 | T | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG00323.hp2 HG01192.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.204-6342T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73838471 | |||||||
chr2:73838706 | G | A | 8 | a0001c0002t0006g0023 a0001c0002t0009g0034 a0001c0002t0009g0035 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-6107G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73838706 | |||||||
chr2:73838884 | C | G | 51 | a0001c0001t0037g0332 a0001c0001t0044g0331 a0001c0002t0003g0001 others(48): Show |
59 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.204-5929C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73838884 | |||||||
chr2:73838885 | T | TTGATTC | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0192 |
3 | HG00642.hp2 HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.204-5913_204-5908d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73838885 | ||||||
chr2:73838961 | G | C | 1 | a0001c0002t0009g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.204-5852G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73838961 | |||||||
chr2:73839014 | T | G | 1 | a0001c0001t0004g0259 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.204-5799T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73839014 | |||||||
chr2:73839156 | T | C | 10 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0014g0026 others(7): Show |
10 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-5657T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73839156 | |||||||
chr2:73839334 | G | A | 113 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(110): Show |
119 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.204-5479G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73839334 | |||||||
chr2:73839537 | C | T | 3 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0284 |
3 | HG00544.hp1 NA19054.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.204-5276C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73839537 | |||||||
chr2:73839981 | T | C | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.204-4832T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73839981 | |||||||
chr2:73840025 | T | G | 1 | a0001c0001t0004g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.204-4788T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840025 | |||||||
chr2:73840135 | A | G | 1 | a0001c0001t0007g0217 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.204-4678A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840135 | |||||||
chr2:73840136 | G | A | 1 | a0001c0001t0007g0217 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.204-4677G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840136 | |||||||
chr2:73840306 | G | A | 4 | a0001c0001t0008g0317 a0001c0001t0008g0318 a0001c0001t0008g0319 others(1): Show |
4 | HG00735.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-4507G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840306 | |||||||
chr2:73840309 | G | GT | 4 | a0001c0001t0002g0230 a0001c0002t0006g0045 a0001c0002t0006g0046 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-4501dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73840309 | ||||||
chr2:73840313 | G | GT | 131 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0084 others(128): Show |
139 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.204-4484dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73840313 | ||||||
chr2:73840313 | G | GTT | 27 | a0001c0001t0002g0081 a0001c0001t0002g0204 a0001c0001t0002g0205 others(24): Show |
30 | HG00140.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.204-4485_204-4484d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73840313 | ||||||
chr2:73840313 | G | T | 5 | a0001c0001t0002g0230 a0001c0001t0018g0207 a0001c0002t0006g0045 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-4500G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840313 | |||||||
chr2:73840313 | GT | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0124 others(13): Show |
16 | HG01257.hp1 HG01884.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.204-4484delT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73840313 | ||||||
chr2:73840332 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | NA18951.hp1 NA18994.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.204-4481G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840332 | |||||||
chr2:73840380 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.204-4433A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840380 | |||||||
chr2:73840433 | T | C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0071 a0001c0002t0005g0072 others(4): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.204-4380T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840433 | |||||||
chr2:73840480 | A | T | 2 | a0001c0001t0022g0209 a0001c0001t0022g0212 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.204-4333A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840480 | |||||||
chr2:73840492 | C | G | 1 | a0001c0001t0036g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.204-4321C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840492 | |||||||
chr2:73840502 | G | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0088 a0001c0001t0001g0089 others(14): Show |
17 | HG00597.hp1 HG01074.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.204-4311G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840502 | |||||||
chr2:73840565 | G | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.204-4248G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840565 | |||||||
chr2:73840579 | A | C | 1 | a0001c0001t0004g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.204-4234A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840579 | |||||||
chr2:73840611 | G | A | 5 | a0001c0002t0009g0034 a0001c0002t0009g0036 a0001c0002t0009g0037 others(2): Show |
5 | HG02647.hp2 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-4202G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840611 | |||||||
chr2:73840636 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.204-4177C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840636 | |||||||
chr2:73840727 | G | T | 1 | a0001c0001t0004g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.204-4086G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840727 | |||||||
chr2:73840749 | A | T | 2 | a0001c0001t0002g0216 a0001c0001t0002g0225 |
2 | NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.204-4064A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840749 | |||||||
chr2:73840753 | A | AT | 17 | a0001c0001t0002g0081 a0001c0001t0003g0324 a0001c0001t0005g0325 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.204-4060_204-4059i others(3): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840753 | |||||||
chr2:73840753 | A | T | 186 | a0001c0001t0001g0096 a0001c0001t0001g0126 a0001c0001t0001g0136 others(183): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.204-4060A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73840753 | |||||||
chr2:73841274 | G | A | 5 | a0001c0001t0002g0245 a0001c0001t0002g0262 a0001c0001t0002g0263 others(2): Show |
5 | NA18948.hp1 NA18960.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-3539G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73841274 | |||||||
chr2:73841366 | G | T | 1 | a0001c0001t0023g0297 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.204-3447G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73841366 | |||||||
chr2:73841827 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.204-2986A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73841827 | |||||||
chr2:73842083 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.204-2730C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842083 | |||||||
chr2:73842108 | TC | T | 12 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.204-2703delC | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73842108 | ||||||
chr2:73842303 | G | A | 11 | a0001c0002t0003g0061 a0001c0002t0003g0078 a0001c0002t0006g0023 others(8): Show |
11 | HG01884.hp1 HG02559.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.204-2510G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842303 | |||||||
chr2:73842400 | TGATGCCA | T | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.204-2412_204-2406d others(9): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842400 | |||||||
chr2:73842428 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.204-2385G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842428 | |||||||
chr2:73842512 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18962.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.204-2301T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842512 | |||||||
chr2:73842796 | T | C | 5 | a0001c0002t0009g0034 a0001c0002t0009g0036 a0001c0002t0009g0037 others(2): Show |
5 | HG02647.hp2 HG02896.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-2017T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842796 | |||||||
chr2:73842911 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.204-1902A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842911 | |||||||
chr2:73842968 | G | A | 1 | a0001c0001t0030g0137 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.204-1845G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73842968 | |||||||
chr2:73843041 | A | G | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-1772A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843041 | |||||||
chr2:73843059 | C | T | 197 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(194): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.204-1754C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843059 | |||||||
chr2:73843064 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.204-1749A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843064 | |||||||
chr2:73843086 | A | G | 1 | a0001c0001t0021g0013 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.204-1727A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843086 | |||||||
chr2:73843115 | C | T | 1 | a0001c0001t0044g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.204-1698C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843115 | |||||||
chr2:73843191 | C | CT | 171 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(168): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.204-1605dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843191 | ||||||
chr2:73843191 | C | CTT | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.204-1606_204-1605d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843191 | ||||||
chr2:73843404 | A | ATG | 4 | a0001c0002t0006g0045 a0001c0002t0006g0046 a0001c0002t0006g0059 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-1407_204-1406d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843404 | ||||||
chr2:73843404 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.204-1409A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843404 | |||||||
chr2:73843406 | G | GTA | 5 | a0001c0001t0002g0081 a0001c0001t0004g0238 a0001c0001t0004g0247 others(2): Show |
5 | HG01070.hp2 HG01175.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1395_204-1394d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATA | 14 | a0001c0001t0002g0290 a0001c0001t0002g0309 a0001c0001t0003g0324 others(11): Show |
14 | HG00741.hp1 HG00741.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.204-1397_204-1394d others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATA | 3 | a0001c0001t0019g0029 a0001c0001t0027g0028 a0001c0002t0009g0035 |
3 | HG01261.hp2 HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.204-1399_204-1394d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(1): Show |
5 | a0001c0001t0023g0295 a0001c0001t0037g0332 a0001c0001t0042g0303 others(2): Show |
5 | HG01192.hp1 HG03209.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1401_204-1394d others(10): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(5): Show |
1 | a0001c0001t0005g0330 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.204-1405_204-1394d others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(7): Show |
3 | a0001c0001t0005g0326 a0001c0001t0008g0315 a0001c0001t0014g0026 |
3 | HG01099.hp2 HG01243.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.204-1394_204-1393i others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(9): Show |
2 | a0001c0001t0005g0325 a0001c0001t0008g0319 |
2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.204-1394_204-1393i others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(11): Show |
1 | a0001c0001t0008g0318 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.204-1394_204-1393i others(20): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(13): Show |
3 | a0001c0001t0008g0317 a0001c0001t0008g0328 a0001c0002t0009g0034 |
3 | HG02451.hp1 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.204-1394_204-1393i others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(15): Show |
2 | a0001c0001t0008g0313 a0001c0002t0009g0037 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.204-1394_204-1393i others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATAT others(17): Show |
3 | a0001c0001t0008g0314 a0001c0002t0009g0038 a0001c0002t0009g0039 |
3 | HG03130.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.204-1394_204-1393i others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTATATGT others(13): Show |
1 | a0001c0002t0009g0036 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.204-1402_204-1401i others(22): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTGTA | 5 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(2): Show |
6 | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-1406_204-1405i others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843406 | G | GTGTATAT others(15): Show |
1 | a0001c0001t0008g0312 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.204-1406_204-1405i others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843406 | ||||||
chr2:73843408 | A | G | 37 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(34): Show |
45 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.204-1405A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843408 | |||||||
chr2:73843410 | A | ATATATAT others(5): Show |
1 | a0001c0002t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.204-1394_204-1393i others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843410 | ||||||
chr2:73843416 | ATATG | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0220 a0001c0001t0002g0221 others(2): Show |
6 | HG01943.hp2 NA18959.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-1393_204-1390d others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843416 | ||||||
chr2:73843418 | ATG | A | 82 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0079 others(79): Show |
86 | HG00423.hp1 HG00544.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.204-1393_204-1392d others(4): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 73843418 | ||||||
chr2:73843420 | G | A | 108 | a0001c0001t0002g0021 a0001c0001t0002g0081 a0001c0001t0002g0204 others(105): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.204-1393G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843420 | |||||||
chr2:73843439 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.204-1374A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843439 | |||||||
chr2:73843502 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.204-1311C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843502 | |||||||
chr2:73843540 | A | T | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-1273A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843540 | |||||||
chr2:73843558 | C | T | 32 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(29): Show |
37 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.204-1255C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843558 | |||||||
chr2:73843716 | T | C | 41 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(38): Show |
49 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.204-1097T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843716 | |||||||
chr2:73843919 | T | C | 32 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(29): Show |
37 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.204-894T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843919 | |||||||
chr2:73843964 | G | A | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-849G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73843964 | |||||||
chr2:73844024 | C | T | 192 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(189): Show |
207 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.204-789C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73844024 | |||||||
chr2:73844280 | C | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0193 |
2 | HG01192.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.204-533C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73844280 | |||||||
chr2:73844364 | T | C | 4 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(1): Show |
5 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-449T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73844364 | |||||||
chr2:73844384 | A | G | 1 | a0001c0002t0006g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.204-429A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73844384 | |||||||
chr2:73844492 | G | A | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.204-321G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 2/9 | chr2 | 73844492 | |||||||
chr2:73844931 | G | A | 4 | a0001c0001t0014g0031 a0001c0001t0014g0032 a0001c0001t0014g0033 others(1): Show |
4 | HG00741.hp2 HG01256.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+43G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 3/9 | chr2 | 73844931 | |||||||
chr2:73844939 | G | A | 2 | a0001c0002t0009g0036 a0001c0002t0009g0037 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.279+51G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 3/9 | chr2 | 73844939 | |||||||
chr2:73844988 | C | T | 1 | a0001c0001t0002g0298 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.279+100C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 3/9 | chr2 | 73844988 | |||||||
chr2:73845008 | A | G | 1 | a0001c0001t0007g0224 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.279+120A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 3/9 | chr2 | 73845008 | |||||||
chr2:73845339 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.375+77A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845339 | |||||||
chr2:73845405 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.375+143A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845405 | |||||||
chr2:73845456 | C | T | 1 | a0001c0001t0015g0182 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.375+194C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845456 | |||||||
chr2:73845633 | A | AT | 65 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0001c0001t0002g0010 others(62): Show |
75 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.375+389dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73845633 | ||||||
chr2:73845633 | A | ATT | 10 | a0001c0001t0008g0317 a0001c0001t0008g0318 a0001c0001t0008g0319 others(7): Show |
10 | HG00735.hp2 HG01261.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+388_375+389dup others(2): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73845633 | ||||||
chr2:73845633 | AT | A | 8 | a0001c0001t0001g0153 a0001c0001t0002g0266 a0001c0001t0002g0292 others(5): Show |
8 | HG01928.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+389delT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73845633 | ||||||
chr2:73845642 | T | G | 12 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0093 others(9): Show |
12 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.375+380T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845642 | |||||||
chr2:73845792 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.375+530C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845792 | |||||||
chr2:73845832 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.375+570A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845832 | |||||||
chr2:73845979 | A | G | 41 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(38): Show |
49 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.375+717A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845979 | |||||||
chr2:73845999 | C | A | 1 | a0001c0001t0013g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.375+737C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73845999 | |||||||
chr2:73846123 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.375+861A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846123 | |||||||
chr2:73846409 | T | TG | 16 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.376-975dupG | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73846409 | ||||||
chr2:73846481 | A | G | 1 | a0001c0001t0036g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.376-906A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846481 | |||||||
chr2:73846504 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0149 |
2 | HG00738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.376-883T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846504 | |||||||
chr2:73846546 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18962.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.376-841C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846546 | |||||||
chr2:73846578 | G | C | 1 | a0001c0001t0004g0235 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.376-809G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846578 | |||||||
chr2:73846625 | G | GA | 117 | a0001c0001t0001g0096 a0001c0001t0002g0010 a0001c0001t0002g0019 others(114): Show |
123 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.376-748dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73846625 | ||||||
chr2:73846666 | G | GTATAAGT others(42): Show |
1 | a0001c0002t0006g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.376-717_376-669dup others(49): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73846666 | ||||||
chr2:73846686 | C | A | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.376-701C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846686 | |||||||
chr2:73846755 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.376-632A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846755 | |||||||
chr2:73846756 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.376-631T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73846756 | |||||||
chr2:73847081 | C | CA | 8 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0130 others(5): Show |
8 | HG01099.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-289dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73847081 | ||||||
chr2:73847081 | C | CAA | 28 | a0001c0001t0002g0216 a0001c0001t0002g0254 a0001c0001t0002g0296 others(25): Show |
28 | HG00733.hp1 HG00741.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.376-290_376-289dup others(2): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73847081 | ||||||
chr2:73847081 | C | CAAA | 103 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(100): Show |
109 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.376-291_376-289dup others(3): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 73847081 | ||||||
chr2:73847117 | A | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0223 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.376-270A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 4/9 | chr2 | 73847117 | |||||||
chr2:73847814 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.742+61C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73847814 | |||||||
chr2:73847953 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.742+200C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73847953 | |||||||
chr2:73848756 | C | T | 2 | a0001c0001t0007g0217 a0001c0001t0007g0244 |
2 | NA18983.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.743-607C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73848756 | |||||||
chr2:73848784 | A | T | 2 | a0001c0001t0037g0332 a0001c0001t0044g0331 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.743-579A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73848784 | |||||||
chr2:73848829 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.743-534C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73848829 | |||||||
chr2:73848913 | T | G | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.743-450T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73848913 | |||||||
chr2:73848916 | G | A | 1 | a0001c0001t0023g0297 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.743-447G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73848916 | |||||||
chr2:73849142 | C | T | 12 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.743-221C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73849142 | |||||||
chr2:73849200 | A | C | 1 | a0001c0001t0002g0289 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.743-163A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73849200 | |||||||
chr2:73849252 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.743-111T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 5/9 | chr2 | 73849252 | |||||||
chr2:73849509 | A | G | 1 | a0001c0001t0019g0027 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.867+22A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849509 | |||||||
chr2:73849564 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.867+77G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849564 | |||||||
chr2:73849789 | A | T | 1 | a0001c0001t0039g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.867+302A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849789 | |||||||
chr2:73849818 | G | A | 13 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0050 others(10): Show |
16 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.867+331G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849818 | |||||||
chr2:73849855 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0030g0137 |
2 | NA18987.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.867+368G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849855 | |||||||
chr2:73849860 | A | G | 1 | a0001c0001t0021g0013 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.867+373A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73849860 | |||||||
chr2:73850212 | T | C | 1 | a0001c0001t0036g0213 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.868-164T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73850212 | |||||||
chr2:73850285 | A | G | 1 | a0001c0001t0002g0286 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.868-91A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73850285 | |||||||
chr2:73850322 | G | A | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.868-54G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73850322 | |||||||
chr2:73850332 | A | G | 2 | a0001c0001t0002g0227 a0001c0001t0002g0265 |
2 | NA18943.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.868-44A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 6/9 | chr2 | 73850332 | |||||||
chr2:73850584 | C | A | 1 | a0001c0001t0002g0289 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1005+71C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73850584 | |||||||
chr2:73850628 | C | G | 4 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(1): Show |
5 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1005+115C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73850628 | |||||||
chr2:73851001 | T | A | 10 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0014g0026 others(7): Show |
10 | HG00741.hp2 HG01243.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1005+488T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851001 | |||||||
chr2:73851103 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1005+590A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851103 | |||||||
chr2:73851108 | G | T | 1 | a0001c0001t0002g0294 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1005+595G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851108 | |||||||
chr2:73851289 | C | T | 2 | a0001c0001t0037g0332 a0001c0001t0044g0331 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1005+776C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851289 | |||||||
chr2:73851381 | G | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0106 a0001c0001t0001g0126 others(1): Show |
4 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1005+868G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851381 | |||||||
chr2:73851423 | C | T | 2 | a0001c0002t0009g0035 a0001c0002t0009g0040 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1005+910C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851423 | |||||||
chr2:73851447 | C | T | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1005+934C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851447 | |||||||
chr2:73851587 | G | T | 115 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(112): Show |
121 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1005+1074G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851587 | |||||||
chr2:73851637 | A | AT | 18 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0180 others(15): Show |
21 | HG01167.hp1 HG01169.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1005+1143dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73851637 | ||||||
chr2:73851637 | AT | A | 20 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0160 others(17): Show |
20 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1005+1143delT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73851637 | ||||||
chr2:73851732 | C | T | 3 | a0001c0001t0019g0027 a0001c0001t0019g0029 a0001c0001t0027g0028 |
3 | HG01261.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1005+1219C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851732 | |||||||
chr2:73851788 | C | T | 27 | a0001c0002t0003g0001 a0001c0002t0003g0041 a0001c0002t0003g0047 others(24): Show |
30 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1005+1275C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851788 | |||||||
chr2:73851862 | A | G | 1 | a0001c0001t0007g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1005+1349A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851862 | |||||||
chr2:73851952 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1005+1439A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73851952 | |||||||
chr2:73852193 | T | C | 70 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(67): Show |
73 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1005+1680T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852193 | |||||||
chr2:73852268 | A | G | 1 | a0001c0001t0004g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1005+1755A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852268 | |||||||
chr2:73852396 | T | C | 1 | a0001c0001t0004g0239 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1005+1883T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852396 | |||||||
chr2:73852406 | C | T | 336 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(333): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1005+1893C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852406 | |||||||
chr2:73852411 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1005+1898G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852411 | |||||||
chr2:73852454 | G | A | 1 | a0001c0001t0014g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1005+1941G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852454 | |||||||
chr2:73852484 | G | A | 16 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+1971G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852484 | |||||||
chr2:73852638 | G | A | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1005+2125G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852638 | |||||||
chr2:73852702 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1005+2189C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852702 | |||||||
chr2:73852740 | C | T | 7 | a0001c0001t0001g0143 a0001c0001t0001g0162 a0001c0001t0002g0290 others(4): Show |
7 | HG00738.hp2 HG01109.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+2227C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852740 | |||||||
chr2:73852763 | C | T | 2 | a0001c0001t0008g0312 a0001c0001t0008g0313 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1005+2250C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852763 | |||||||
chr2:73852787 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1005+2274C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852787 | |||||||
chr2:73852829 | C | T | 1 | a0001c0002t0009g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1005+2316C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852829 | |||||||
chr2:73852845 | T | TTG | 112 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
122 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1005+2368_1005+236 others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTG | 48 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0102 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.1005+2366_1005+236 others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTGTG | 13 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0130 others(10): Show |
13 | HG00438.hp2 HG00621.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1005+2364_1005+236 others(10): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0008g0312 a0001c0001t0008g0319 a0001c0001t0022g0209 others(8): Show |
14 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1005+2362_1005+236 others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0008g0313 a0001c0001t0008g0317 a0002c0004t0003g0068 |
3 | HG02071.hp1 HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1005+2360_1005+236 others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0008g0318 a0001c0001t0008g0328 |
2 | HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1005+2358_1005+236 others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0044g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1005+2356_1005+236 others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | TTG | T | 8 | a0001c0001t0001g0109 a0001c0001t0001g0144 a0001c0001t0001g0176 others(5): Show |
9 | HG00544.hp2 HG02165.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.1005+2368_1005+236 others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | TTGTG | T | 102 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0081 others(99): Show |
107 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1005+2366_1005+236 others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0280 others(2): Show |
5 | HG00544.hp1 NA19012.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+2362_1005+236 others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | TTGTGTGT others(5): Show |
T | 16 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+2358_1005+236 others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852845 | TTGTGTGT others(7): Show |
T | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1005+2356_1005+236 others(18): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852845 | ||||||
chr2:73852911 | T | A | 1 | a0001c0001t0004g0272 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1005+2398T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852911 | |||||||
chr2:73852917 | G | GGT | 29 | a0001c0001t0001g0113 a0001c0001t0001g0122 a0001c0001t0001g0124 others(26): Show |
29 | HG00544.hp2 HG00735.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1005+2441_1005+244 others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | G | GGTGT | 12 | a0001c0001t0001g0160 a0001c0001t0002g0284 a0001c0001t0007g0306 others(9): Show |
13 | HG00544.hp1 HG00738.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1005+2439_1005+244 others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | G | GGTGTGT | 23 | a0001c0001t0002g0206 a0001c0001t0002g0240 a0001c0001t0002g0241 others(20): Show |
23 | HG01109.hp2 HG01884.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.1005+2437_1005+244 others(10): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | G | GGTGTGTG others(1): Show |
55 | a0001c0001t0002g0010 a0001c0001t0002g0021 a0001c0001t0002g0080 others(52): Show |
59 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1005+2435_1005+244 others(12): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | G | GGTGTGTG others(3): Show |
15 | a0001c0001t0002g0019 a0001c0001t0002g0079 a0001c0001t0002g0220 others(12): Show |
16 | HG00733.hp1 HG00741.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+2433_1005+244 others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | G | GGTGTGTG others(5): Show |
11 | a0001c0001t0002g0215 a0001c0001t0002g0223 a0001c0001t0002g0227 others(8): Show |
11 | HG01943.hp2 HG02300.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1005+2431_1005+244 others(16): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | GGT | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0001g0149 others(2): Show |
5 | HG00738.hp1 HG03516.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1005+2441_1005+244 others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | GGTGT | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0119 a0001c0001t0004g0269 |
3 | HG01496.hp2 HG02735.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1005+2439_1005+244 others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1005+2433_1005+244 others(14): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | GGTGTGTG others(13): Show |
G | 42 | a0001c0001t0030g0137 a0001c0002t0003g0001 a0001c0002t0003g0041 others(39): Show |
50 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1005+2423_1005+244 others(24): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852917 | GGTGTGTG others(15): Show |
G | 16 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(13): Show |
16 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1005+2421_1005+244 others(26): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73852917 | ||||||
chr2:73852971 | T | A | 1 | a0001c0001t0044g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1005+2458T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73852971 | |||||||
chr2:73853025 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1005+2512G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853025 | |||||||
chr2:73853032 | T | C | 197 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(194): Show |
212 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1005+2519T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853032 | |||||||
chr2:73853138 | C | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1005+2625C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853138 | |||||||
chr2:73853207 | G | C | 2 | a0001c0001t0023g0295 a0001c0001t0023g0297 |
2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1005+2694G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853207 | |||||||
chr2:73853246 | A | T | 52 | a0001c0001t0030g0137 a0001c0001t0037g0332 a0001c0001t0044g0331 others(49): Show |
60 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1005+2733A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853246 | |||||||
chr2:73853285 | T | C | 2 | a0001c0001t0037g0332 a0001c0001t0044g0331 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1005+2772T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853285 | |||||||
chr2:73853312 | G | T | 1 | a0001c0002t0003g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1005+2799G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853312 | |||||||
chr2:73853411 | G | T | 111 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(108): Show |
117 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1005+2898G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853411 | |||||||
chr2:73853440 | T | C | 2 | a0001c0001t0002g0215 a0001c0001t0002g0223 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1005+2927T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853440 | |||||||
chr2:73853591 | G | A | 2 | a0001c0001t0008g0314 a0001c0001t0008g0315 |
2 | HG01361.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1005+3078G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853591 | |||||||
chr2:73853774 | A | G | 3 | a0001c0002t0006g0045 a0001c0002t0006g0046 a0001c0002t0006g0059 |
3 | HG02145.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1005+3261A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853774 | |||||||
chr2:73853889 | T | C | 1 | a0003c0007t0026g0316 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1005+3376T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853889 | |||||||
chr2:73853958 | A | G | 1 | a0001c0002t0005g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1005+3445A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73853958 | |||||||
chr2:73854051 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1005+3538A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73854051 | |||||||
chr2:73854127 | G | A | 8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1005+3614G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73854127 | |||||||
chr2:73855014 | C | A | 1 | a0001c0001t0042g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1006-4240C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855014 | |||||||
chr2:73855019 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1006-4235C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855019 | |||||||
chr2:73855206 | A | G | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1006-4048A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855206 | |||||||
chr2:73855290 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1006-3964C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855290 | |||||||
chr2:73855316 | G | C | 3 | a0001c0002t0009g0034 a0001c0002t0009g0038 a0001c0002t0009g0039 |
3 | HG03130.hp2 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1006-3938G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855316 | |||||||
chr2:73855386 | G | A | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-3868G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855386 | |||||||
chr2:73855593 | A | G | 10 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
10 | HG01891.hp2 HG02486.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006-3661A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855593 | |||||||
chr2:73855943 | T | C | 1 | a0001c0001t0004g0261 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1006-3311T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73855943 | |||||||
chr2:73856031 | A | T | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-3223A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856031 | |||||||
chr2:73856100 | T | C | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-3154T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856100 | |||||||
chr2:73856113 | T | C | 2 | a0001c0001t0002g0215 a0001c0001t0002g0223 |
2 | NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1006-3141T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856113 | |||||||
chr2:73856114 | C | T | 1 | a0001c0001t0015g0182 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1006-3140C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856114 | |||||||
chr2:73856383 | A | G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0196 others(2): Show |
5 | HG00639.hp1 HG00642.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-2871A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856383 | |||||||
chr2:73856716 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1006-2538A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856716 | |||||||
chr2:73856770 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1006-2484C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856770 | |||||||
chr2:73856781 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1006-2473A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856781 | |||||||
chr2:73856880 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1006-2374T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856880 | |||||||
chr2:73856928 | C | A | 1 | a0001c0001t0021g0013 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1006-2326C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73856928 | |||||||
chr2:73857232 | C | T | 52 | a0001c0001t0002g0277 a0001c0001t0030g0137 a0001c0001t0037g0332 others(49): Show |
60 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1006-2022C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857232 | |||||||
chr2:73857239 | T | C | 19 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(16): Show |
19 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1006-2015T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857239 | |||||||
chr2:73857289 | A | T | 1 | a0001c0001t0014g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1006-1965A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857289 | |||||||
chr2:73857307 | C | G | 13 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(10): Show |
14 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1006-1947C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857307 | |||||||
chr2:73857390 | A | T | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-1864A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857390 | |||||||
chr2:73857667 | T | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0001g0133 |
3 | HG01255.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1006-1587T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857667 | |||||||
chr2:73857704 | A | G | 3 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 |
3 | HG02895.hp1 HG02897.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1006-1550A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857704 | |||||||
chr2:73857806 | T | C | 1 | a0001c0001t0006g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1006-1448T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857806 | |||||||
chr2:73857819 | C | T | 2 | a0001c0001t0004g0234 a0001c0001t0004g0251 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1006-1435C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857819 | |||||||
chr2:73857974 | A | G | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-1280A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73857974 | |||||||
chr2:73858027 | G | C | 42 | a0001c0001t0030g0137 a0001c0002t0003g0001 a0001c0002t0003g0041 others(39): Show |
50 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1006-1227G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858027 | |||||||
chr2:73858044 | G | A | 17 | a0001c0001t0003g0324 a0001c0001t0005g0325 a0001c0001t0005g0326 others(14): Show |
17 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006-1210G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858044 | |||||||
chr2:73858045 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01081.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1006-1209C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858045 | |||||||
chr2:73858101 | A | G | 196 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(193): Show |
211 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1006-1153A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858101 | |||||||
chr2:73858159 | A | AT | 11 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0154 others(8): Show |
11 | HG02145.hp1 HG03017.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.1006-1069dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73858159 | ||||||
chr2:73858159 | AT | A | 22 | a0001c0001t0001g0104 a0001c0001t0001g0140 a0001c0001t0002g0216 others(19): Show |
22 | HG01884.hp1 HG01981.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1006-1069delT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73858159 | ||||||
chr2:73858159 | ATT | A | 167 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(164): Show |
182 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.1006-1070_1006-106 others(6): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73858159 | ||||||
chr2:73858159 | ATTT | A | 7 | a0001c0001t0002g0220 a0001c0001t0002g0266 a0001c0001t0002g0311 others(4): Show |
7 | HG01168.hp1 HG01256.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006-1071_1006-106 others(7): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73858159 | ||||||
chr2:73858519 | T | C | 1 | a0001c0001t0011g0320 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1006-735T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858519 | |||||||
chr2:73858596 | T | C | 1 | a0001c0001t0007g0308 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1006-658T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858596 | |||||||
chr2:73858769 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1006-485G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858769 | |||||||
chr2:73858891 | C | G | 2 | a0001c0001t0001g0110 a0001c0001t0014g0026 |
2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1006-363C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858891 | |||||||
chr2:73858898 | C | A | 12 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(9): Show |
13 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1006-356C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858898 | |||||||
chr2:73858900 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0267 |
2 | NA18981.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1006-354T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858900 | |||||||
chr2:73858919 | A | AC | 21 | a0001c0001t0002g0291 a0001c0001t0005g0325 a0001c0001t0005g0326 others(18): Show |
23 | HG01099.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1006-329dupC | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 73858919 | ||||||
chr2:73858940 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1006-314A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858940 | |||||||
chr2:73858987 | C | T | 1 | a0001c0001t0006g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1006-267C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73858987 | |||||||
chr2:73859220 | G | A | 1 | a0001c0001t0002g0266 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1006-34G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 7/9 | chr2 | 73859220 | |||||||
chr2:73859423 | T | G | 5 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(2): Show |
6 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118+57T>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859423 | |||||||
chr2:73859532 | T | A | 46 | a0001c0001t0003g0324 a0001c0001t0008g0312 a0001c0001t0008g0313 others(43): Show |
51 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1118+166T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859532 | |||||||
chr2:73859560 | C | A | 49 | a0001c0001t0004g0005 a0001c0001t0004g0222 a0001c0001t0004g0231 others(46): Show |
53 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.1118+194C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859560 | |||||||
chr2:73859706 | A | T | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1118+340A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859706 | |||||||
chr2:73859709 | A | T | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1118+343A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859709 | |||||||
chr2:73859712 | T | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1119-340T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859712 | |||||||
chr2:73859714 | T | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1119-338T>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859714 | |||||||
chr2:73859714 | T | TAATAAAA others(1): Show |
168 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(165): Show |
180 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1119-329_1119-322d others(10): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 73859714 | ||||||
chr2:73859725 | T | TAAAAAA | 8 | a0001c0001t0041g0310 a0001c0002t0005g0002 a0001c0002t0005g0071 others(5): Show |
11 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1119-322_1119-321i others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 73859725 | ||||||
chr2:73859845 | A | T | 1 | a0001c0002t0005g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1119-207A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859845 | |||||||
chr2:73859854 | A | C | 2 | a0001c0001t0022g0209 a0001c0001t0022g0212 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1119-198A>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859854 | |||||||
chr2:73859957 | G | T | 1 | a0001c0001t0012g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119-95G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | chr2 | 73859957 | |||||||
chr2:73860038 | T | TTTTTTTT others(1169): Show |
2 | a0001c0001t0027g0028 a0001c0001t0044g0331 |
2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1119-10_1119-9insT others(1175): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 73860038 | ||||||
chr2:73860038 | T | TTTTTTTT others(1169): Show |
8 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(5): Show |
8 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1119-10_1119-9insT others(1175): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 73860038 | ||||||
chr2:73860163 | T | C | 50 | a0001c0001t0004g0005 a0001c0001t0004g0222 a0001c0001t0004g0231 others(47): Show |
54 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1218+12T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860163 | |||||||
chr2:73860171 | A | G | 83 | a0001c0001t0002g0010 a0001c0001t0002g0019 a0001c0001t0002g0021 others(80): Show |
86 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1218+20A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860171 | |||||||
chr2:73860174 | A | G | 1 | a0001c0001t0012g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1218+23A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860174 | |||||||
chr2:73860193 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1218+42A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860193 | |||||||
chr2:73860202 | A | G | 15 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(12): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+51A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860202 | |||||||
chr2:73860238 | C | G | 1 | a0001c0001t0040g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1218+87C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860238 | |||||||
chr2:73860247 | G | A | 10 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(7): Show |
10 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+96G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860247 | |||||||
chr2:73860250 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1218+99C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860250 | |||||||
chr2:73860378 | G | A | 10 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 others(7): Show |
10 | HG01884.hp1 HG02647.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218+227G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860378 | |||||||
chr2:73860473 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1218+322G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860473 | |||||||
chr2:73860583 | C | A | 15 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(12): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1218+432C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860583 | |||||||
chr2:73860585 | G | T | 1 | a0001c0001t0037g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1218+434G>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860585 | |||||||
chr2:73860778 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1218+627A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860778 | |||||||
chr2:73860841 | T | C | 2 | a0001c0001t0002g0291 a0001c0001t0043g0305 |
2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1218+690T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860841 | |||||||
chr2:73860949 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1218+798C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73860949 | |||||||
chr2:73861324 | T | C | 1 | a0001c0002t0009g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1219-879T>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861324 | |||||||
chr2:73861351 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1219-852A>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861351 | |||||||
chr2:73861388 | A | G | 10 | a0001c0001t0041g0310 a0001c0002t0005g0002 a0001c0002t0005g0070 others(7): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1219-815A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861388 | |||||||
chr2:73861442 | A | G | 1 | a0001c0001t0042g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1219-761A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861442 | |||||||
chr2:73861451 | C | G | 1 | a0001c0001t0003g0324 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1219-752C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861451 | |||||||
chr2:73861471 | C | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1219-732C>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861471 | |||||||
chr2:73861504 | T | TTTTTTG | 5 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0002g0226 others(2): Show |
5 | HG00423.hp1 HG01515.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219-671_1219-666d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73861504 | ||||||
chr2:73861504 | TTTTTTG | T | 10 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(7): Show |
10 | HG00735.hp2 HG01361.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-671_1219-666d others(8): Show |
STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73861504 | ||||||
chr2:73861554 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1219-649C>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861554 | |||||||
chr2:73861636 | A | G | 1 | a0001c0001t0037g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1219-567A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861636 | |||||||
chr2:73861644 | G | C | 10 | a0001c0001t0041g0310 a0001c0002t0005g0002 a0001c0002t0005g0070 others(7): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1219-559G>C | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861644 | |||||||
chr2:73861665 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1219-538C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861665 | |||||||
chr2:73861668 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1219-535G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861668 | |||||||
chr2:73861671 | G | A | 5 | a0001c0001t0011g0022 a0001c0001t0011g0320 a0001c0001t0011g0321 others(2): Show |
6 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1219-532G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861671 | |||||||
chr2:73861686 | A | AT | 55 | a0001c0001t0001g0085 a0001c0001t0001g0092 a0001c0001t0001g0116 others(52): Show |
60 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.1219-495dupT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73861686 | ||||||
chr2:73861686 | AT | A | 12 | a0001c0001t0001g0148 a0001c0001t0002g0211 a0001c0001t0002g0257 others(9): Show |
13 | HG00099.hp1 HG01070.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1219-495delT | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73861686 | ||||||
chr2:73861714 | G | A | 15 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(12): Show |
16 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1219-489G>A | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861714 | |||||||
chr2:73861865 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1219-338C>T | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861865 | |||||||
chr2:73861901 | A | G | 45 | a0001c0001t0008g0312 a0001c0001t0008g0313 a0001c0001t0008g0314 others(42): Show |
50 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.1219-302A>G | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | chr2 | 73861901 | |||||||
chr2:73862139 | G | GA | 10 | a0001c0001t0018g0207 a0001c0001t0018g0208 a0001c0001t0018g0210 others(7): Show |
10 | HG01884.hp1 HG02647.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-50dupA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73862139 | ||||||
chr2:73862139 | GA | G | 6 | a0001c0001t0001g0117 a0001c0001t0011g0022 a0001c0001t0011g0320 others(3): Show |
7 | HG00099.hp1 HG00323.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1219-50delA | STAMBP | ENSG00000124356.17 | transcript | ENST00000394070.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 73862139 |