Item | Value |
---|---|
geneid | 123722 |
ensemblid | ENSG00000186628.12 |
hgncid | 18024 |
symbol | FSD2 |
name | fibronectin type III and SPRY domain containing 2 |
refseq_nuc | NM_001007122.4 |
refseq_prot | NP_001007123.1 |
ensembl_nuc | ENST00000334574.12 |
ensembl_prot | ENSP00000335651.8 |
mane_status | MANE Select |
chr | chr15 |
start | 82755362 |
end | 82806069 |
strand | - |
ver | v1.2 |
region | chr15:82755362-82806069 |
region5000 | chr15:82750362-82811069 |
regionname0 | FSD2_chr15_82755362_82806069 |
regionname5000 | FSD2_chr15_82750362_82811069 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 749 | 300 | 77 | 53 | 132 | 13 | 24 | 100 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0002 | 0/0 | 749 | 53 | 0 | 11 | 33 | 1 | 8 | 24 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0003 | 0/1 | 749 | 22 | 7 | 9 | 0 | 3 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0004 | 0/0 | 749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0005 | 0/0 | 749 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0006 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0007 | 0/0 | 749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0008 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
a0009 | 0/0 | 305 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(300): Show |
chr15 | 82750362 | 82811069 |
a0010 | 0/0 | 749 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | MEEES others(744): Show |
chr15 | 82750362 | 82811069 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2247 | 199 | 56 | 32 | 84 | 8 | 18 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0001c0002 | 0/0 | 2247 | 92 | 18 | 18 | 47 | 5 | 4 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0001c0005 | 0/0 | 2247 | 5 | 0 | 3 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0001c0008 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0001c0011 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0001c0012 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0002c0003 | 0/0 | 2247 | 53 | 0 | 11 | 33 | 1 | 8 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0003c0004 | 0/1 | 2247 | 22 | 7 | 9 | 0 | 3 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0004c0006 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0005c0007 | 0/0 | 2247 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0006c0013 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0007c0015 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0008c0014 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 | ||
a0009c0010 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2262): Show |
chr15 | 82750362 | 82811069 | ||
a0010c0009 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGGA others(2242): Show |
chr15 | 82750362 | 82811069 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 6418 | 59 | 9 | 9 | 22 | 3 | 15 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0003 | 0/0 | 6417 | 55 | 4 | 8 | 41 | 1 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0005 | 0/0 | 6419 | 11 | 4 | 4 | 0 | 2 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0008 | 0/0 | 6416 | 8 | 8 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0009 | 0/0 | 6420 | 8 | 1 | 5 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6415): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0010 | 0/0 | 6417 | 7 | 0 | 0 | 7 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0011 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0012 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0013 | 0/0 | 6419 | 6 | 6 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0014 | 0/0 | 6418 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0015 | 0/0 | 6420 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6415): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0017 | 0/0 | 6417 | 3 | 3 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0021 | 0/0 | 6417 | 3 | 1 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0023 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0024 | 0/0 | 6419 | 3 | 0 | 3 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0025 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0026 | 0/0 | 6416 | 2 | 1 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0027 | 0/0 | 6418 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0028 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0029 | 0/0 | 6416 | 2 | 0 | 1 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0030 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0031 | 0/0 | 6420 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6415): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0035 | 0/0 | 6417 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0036 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0037 | 0/0 | 6418 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0042 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0043 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0044 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0048 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0052 | 0/0 | 6418 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0056 | 0/0 | 6420 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6415): Show |
chr15 | 82750362 | 82811069 |
a0001c0001t0060 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0001 | 0/0 | 6416 | 66 | 17 | 15 | 28 | 4 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0007 | 0/0 | 6416 | 10 | 0 | 0 | 10 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0016 | 0/0 | 6415 | 4 | 0 | 0 | 2 | 1 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6410): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0022 | 0/0 | 6417 | 3 | 0 | 2 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0034 | 0/0 | 6415 | 2 | 0 | 0 | 2 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6410): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0053 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0054 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0055 | 0/0 | 6418 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0057 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0058 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0059 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0002t0061 | 0/0 | 6416 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0005t0011 | 0/0 | 6417 | 5 | 0 | 3 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0001c0008t0023 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0001c0011t0008 | 0/0 | 6416 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0001c0012t0001 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0004 | 0/0 | 6417 | 38 | 0 | 9 | 22 | 0 | 7 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0012 | 0/0 | 6417 | 5 | 0 | 1 | 3 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0018 | 0/0 | 6418 | 3 | 0 | 1 | 1 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0019 | 0/0 | 6417 | 3 | 0 | 0 | 3 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0038 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0039 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0040 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0002c0003t0041 | 0/0 | 6416 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0006 | 0/0 | 6418 | 10 | 3 | 5 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0011 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0020 | 0/0 | 6418 | 3 | 0 | 1 | 0 | 2 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0032 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0045 | 0/0 | 6419 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0046 | 0/0 | 6418 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0047 | 0/0 | 6417 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0049 | 0/0 | 6416 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0050 | 0/0 | 6418 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6413): Show |
chr15 | 82750362 | 82811069 |
a0003c0004t0051 | 0/1 | 6416 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0004c0006t0001 | 0/0 | 6416 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6411): Show |
chr15 | 82750362 | 82811069 |
a0005c0007t0033 | 0/0 | 6419 | 2 | 2 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6414): Show |
chr15 | 82750362 | 82811069 |
a0006c0013t0004 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0007c0015t0004 | 0/0 | 6417 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0008c0014t0004 | 0/0 | 6417 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
a0009c0010t0004 | 0/0 | 6437 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6432): Show |
chr15 | 82750362 | 82811069 |
a0010c0009t0003 | 0/0 | 6417 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | ATGCA others(6412): Show |
chr15 | 82750362 | 82811069 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 1/0 | 3 | 0 | 0 | 1 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0012g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0013g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0014g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0015g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0017g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0021g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0023g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0024g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0025g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0025g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0026g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0026g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0027g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0027g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0028g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0028g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0029g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0029g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0030g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0030g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0031g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0031g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0035g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0035g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0036g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0037g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0042g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0043g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0044g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0048g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0052g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0056g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0001t0060g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0016g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0022g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0034g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0034g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0053g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0054g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0055g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0057g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0058g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0059g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0002t0061g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0005t0011g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0008t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0008t0023g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0011t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0001c0012t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0012g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0018g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0019g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0038g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0039g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0040g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0002c0003t0041g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0011g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0020g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0032g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0032g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0045g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0046g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0047g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0049g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0050g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0003c0004t0051g0369 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0004c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0004c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0005c0007t0033g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0005c0007t0033g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0006c0013t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0007c0015t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0008c0014t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0009c0010t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
a0010c0009t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0018 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0064 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | GBR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00280 | hp1 | a0002 | c0003 | t0012 | g0355 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00323 | hp2 | a0003 | c0004 | t0049 | g0130 | EUR | FIN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00423 | hp1 | a0001 | c0002 | t0007 | g0317 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00423 | hp2 | a0002 | c0003 | t0004 | g0338 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00438 | hp1 | a0006 | c0013 | t0004 | g0080 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00544 | hp1 | a0002 | c0003 | t0004 | g0220 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00639 | hp2 | a0001 | c0005 | t0011 | g0371 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00673 | hp1 | a0001 | c0002 | t0007 | g0142 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00733 | hp2 | a0002 | c0003 | t0004 | g0368 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00735 | hp1 | a0001 | c0005 | t0011 | g0372 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00735 | hp2 | a0007 | c0015 | t0004 | g0144 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00738 | hp2 | a0003 | c0004 | t0046 | g0128 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00741 | hp1 | a0003 | c0004 | t0045 | g0140 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0319 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01070 | hp1 | a0001 | c0001 | t0024 | g0374 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01070 | hp2 | a0001 | c0001 | t0029 | g0206 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01071 | hp2 | a0001 | c0001 | t0024 | g0373 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01074 | hp2 | a0003 | c0004 | t0020 | g0221 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01099 | hp1 | a0003 | c0004 | t0006 | g0177 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01109 | hp1 | a0001 | c0002 | t0022 | g0223 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01109 | hp2 | a0001 | c0001 | t0026 | g0248 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01167 | hp2 | a0003 | c0004 | t0006 | g0004 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01169 | hp1 | a0003 | c0004 | t0006 | g0004 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01175 | hp2 | a0002 | c0003 | t0004 | g0359 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0049 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01258 | hp1 | a0003 | c0004 | t0006 | g0132 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01258 | hp2 | a0001 | c0001 | t0009 | g0010 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01261 | hp2 | a0001 | c0001 | t0024 | g0375 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01358 | hp2 | a0003 | c0004 | t0006 | g0131 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01361 | hp1 | a0001 | c0001 | t0009 | g0021 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01361 | hp2 | a0001 | c0005 | t0011 | g0370 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0027 | AMR | CLM | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0016 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01515 | hp2 | a0003 | c0004 | t0020 | g0133 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0019 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01516 | hp2 | a0001 | c0002 | t0016 | g0065 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0058 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01517 | hp2 | a0003 | c0004 | t0020 | g0135 | EUR | IBS | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01884 | hp2 | a0001 | c0008 | t0023 | g0284 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01891 | hp1 | a0001 | c0001 | t0023 | g0008 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01928 | hp1 | a0002 | c0003 | t0004 | g0145 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01934 | hp1 | a0002 | c0003 | t0004 | g0005 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01934 | hp2 | a0001 | c0001 | t0037 | g0262 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01943 | hp2 | a0002 | c0003 | t0004 | g0005 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01952 | hp1 | a0001 | c0002 | t0022 | g0092 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01975 | hp1 | a0002 | c0003 | t0012 | g0354 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01975 | hp2 | a0001 | c0002 | t0061 | g0109 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01978 | hp2 | a0002 | c0003 | t0018 | g0356 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01993 | hp1 | a0002 | c0003 | t0004 | g0351 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02004 | hp1 | a0001 | c0001 | t0009 | g0022 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02015 | hp2 | a0002 | c0003 | t0004 | g0337 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02040 | hp2 | a0002 | c0003 | t0004 | g0340 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02071 | hp1 | a0002 | c0003 | t0019 | g0331 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02083 | hp1 | a0002 | c0003 | t0004 | g0345 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02132 | hp2 | a0002 | c0003 | t0038 | g0366 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02148 | hp1 | a0002 | c0003 | t0004 | g0361 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02165 | hp1 | a0002 | c0003 | t0004 | g0339 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02165 | hp2 | a0001 | c0002 | t0007 | g0271 | EAS | CDX | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0217 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02273 | hp1 | a0003 | c0004 | t0011 | g0031 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02293 | hp2 | a0002 | c0003 | t0004 | g0330 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02300 | hp2 | a0002 | c0003 | t0004 | g0326 | AMR | PEL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0212 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02572 | hp1 | a0001 | c0001 | t0015 | g0276 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02572 | hp2 | a0003 | c0004 | t0050 | g0134 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02602 | hp1 | a0002 | c0003 | t0004 | g0352 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02615 | hp2 | a0003 | c0004 | t0006 | g0009 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0241 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0213 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0026 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02698 | hp1 | a0003 | c0004 | t0006 | g0176 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02717 | hp1 | a0001 | c0001 | t0042 | g0032 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02735 | hp1 | a0001 | c0002 | t0016 | g0085 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02809 | hp1 | a0003 | c0004 | t0032 | g0124 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0164 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02895 | hp2 | a0003 | c0004 | t0047 | g0129 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02896 | hp1 | a0001 | c0001 | t0031 | g0215 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0325 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02922 | hp2 | a0004 | c0006 | t0001 | g0099 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02965 | hp1 | a0001 | c0008 | t0023 | g0285 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0175 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02976 | hp1 | a0001 | c0001 | t0031 | g0216 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02976 | hp2 | a0001 | c0001 | t0013 | g0322 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03041 | hp1 | a0001 | c0001 | t0015 | g0218 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0234 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03098 | hp2 | a0001 | c0001 | t0048 | g0272 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03139 | hp2 | a0001 | c0001 | t0043 | g0163 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03195 | hp1 | a0003 | c0004 | t0006 | g0152 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03195 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | ESN | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0280 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0265 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03225 | hp1 | a0001 | c0001 | t0015 | g0219 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03453 | hp1 | a0001 | c0002 | t0057 | g0102 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03486 | hp2 | a0001 | c0001 | t0030 | g0286 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03490 | hp1 | a0001 | c0005 | t0011 | g0006 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03492 | hp1 | a0001 | c0005 | t0011 | g0006 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03540 | hp2 | a0001 | c0001 | t0026 | g0250 | AFR | GWD | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03579 | hp1 | a0001 | c0001 | t0030 | g0287 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03579 | hp2 | a0001 | c0001 | t0060 | g0123 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03654 | hp2 | a0002 | c0003 | t0004 | g0346 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03704 | hp2 | a0002 | c0003 | t0018 | g0344 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03710 | hp1 | a0003 | c0004 | t0006 | g0125 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03831 | hp2 | a0002 | c0003 | t0004 | g0279 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0074 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04115 | hp1 | a0002 | c0003 | t0004 | g0365 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04184 | hp1 | a0001 | c0002 | t0055 | g0068 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04184 | hp2 | a0002 | c0003 | t0004 | g0358 | SAS | BEB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04199 | hp1 | a0002 | c0003 | t0004 | g0332 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04199 | hp2 | a0001 | c0001 | t0052 | g0313 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | STU | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18522 | hp1 | a0001 | c0001 | t0014 | g0001 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18612 | hp1 | a0002 | c0003 | t0004 | g0324 | EAS | CHB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0233 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18942 | hp1 | a0002 | c0003 | t0004 | g0333 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18944 | hp2 | a0002 | c0003 | t0004 | g0110 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18945 | hp1 | a0001 | c0012 | t0001 | g0063 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18945 | hp2 | a0002 | c0003 | t0004 | g0367 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18947 | hp1 | a0001 | c0002 | t0058 | g0052 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18953 | hp2 | a0002 | c0003 | t0039 | g0323 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18956 | hp2 | a0001 | c0002 | t0034 | g0071 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18957 | hp2 | a0001 | c0002 | t0007 | g0043 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18963 | hp1 | a0001 | c0002 | t0034 | g0033 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18963 | hp2 | a0001 | c0001 | t0027 | g0321 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18964 | hp1 | a0001 | c0001 | t0021 | g0210 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0196 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18966 | hp2 | a0001 | c0002 | t0007 | g0034 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18969 | hp2 | a0002 | c0003 | t0018 | g0342 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18970 | hp1 | a0001 | c0001 | t0012 | g0228 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18970 | hp2 | a0002 | c0003 | t0004 | g0224 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18972 | hp1 | a0001 | c0002 | t0022 | g0115 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18973 | hp1 | a0001 | c0001 | t0021 | g0300 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18975 | hp1 | a0002 | c0003 | t0004 | g0348 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18978 | hp1 | a0002 | c0003 | t0012 | g0360 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18979 | hp2 | a0002 | c0003 | t0004 | g0334 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18981 | hp2 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18982 | hp1 | a0001 | c0001 | t0025 | g0253 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18982 | hp2 | a0001 | c0002 | t0016 | g0116 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18983 | hp2 | a0001 | c0001 | t0010 | g0194 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18986 | hp1 | a0001 | c0002 | t0016 | g0091 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18986 | hp2 | a0001 | c0001 | t0028 | g0198 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18991 | hp1 | a0001 | c0002 | t0053 | g0107 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18997 | hp1 | a0002 | c0003 | t0041 | g0362 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18997 | hp2 | a0001 | c0001 | t0010 | g0143 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19000 | hp1 | a0002 | c0003 | t0004 | g0267 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19000 | hp2 | a0001 | c0002 | t0054 | g0045 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19001 | hp2 | a0001 | c0001 | t0035 | g0246 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19002 | hp2 | a0002 | c0003 | t0019 | g0357 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19005 | hp1 | a0001 | c0002 | t0007 | g0316 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19005 | hp2 | a0002 | c0003 | t0004 | g0168 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19009 | hp1 | a0001 | c0001 | t0035 | g0229 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19010 | hp2 | a0002 | c0003 | t0012 | g0329 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19011 | hp1 | a0001 | c0002 | t0007 | g0044 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19030 | hp2 | a0001 | c0001 | t0056 | g0121 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19043 | hp1 | a0005 | c0007 | t0033 | g0047 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0237 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19054 | hp1 | a0002 | c0003 | t0019 | g0364 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19054 | hp2 | a0001 | c0002 | t0007 | g0310 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19055 | hp2 | a0002 | c0003 | t0004 | g0251 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19057 | hp2 | a0002 | c0003 | t0004 | g0082 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19058 | hp1 | a0001 | c0001 | t0036 | g0188 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19065 | hp1 | a0001 | c0002 | t0007 | g0042 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19065 | hp2 | a0002 | c0003 | t0004 | g0349 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19067 | hp1 | a0001 | c0001 | t0010 | g0193 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19072 | hp1 | a0001 | c0001 | t0025 | g0227 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19072 | hp2 | a0001 | c0002 | t0007 | g0048 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19074 | hp1 | a0001 | c0001 | t0029 | g0191 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19074 | hp2 | a0002 | c0003 | t0004 | g0343 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19076 | hp1 | a0001 | c0001 | t0027 | g0244 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19081 | hp1 | a0002 | c0003 | t0040 | g0225 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19081 | hp2 | a0009 | c0010 | t0004 | g0350 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19084 | hp1 | a0002 | c0003 | t0004 | g0335 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19084 | hp2 | a0001 | c0002 | t0059 | g0051 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19085 | hp2 | a0002 | c0003 | t0012 | g0336 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19088 | hp2 | a0002 | c0003 | t0004 | g0347 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0182 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19091 | hp1 | a0001 | c0001 | t0028 | g0195 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19091 | hp2 | a0002 | c0003 | t0004 | g0341 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19240 | hp1 | a0001 | c0001 | t0013 | g0165 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | YRI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20129 | hp1 | a0001 | c0001 | t0013 | g0173 | AFR | ASW | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ASW | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20752 | hp1 | a0001 | c0001 | t0009 | g0020 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0305 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0067 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20805 | hp2 | a0010 | c0009 | t0003 | g0226 | EUR | TSI | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20905 | hp1 | a0002 | c0003 | t0004 | g0363 | SAS | GIH | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | GIH | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02109 | hp2 | a0003 | c0004 | t0006 | g0153 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02486 | hp1 | a0003 | c0004 | t0032 | g0136 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0312 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03471 | hp1 | a0005 | c0007 | t0033 | g0028 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG03471 | hp2 | a0001 | c0011 | t0008 | g0222 | AFR | MSL | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
HG06807 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA18955 | hp2 | a0008 | c0014 | t0004 | g0245 | EAS | JPT | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20300 | hp1 | a0001 | c0001 | t0044 | g0162 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | USA | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0098 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | LWK | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
homoSapiens | chm13v2 | a0003 | c0004 | t0051 | g0369 | REF | REF | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | FSD2_chr15_82750362_82811069 | FSD2 | chr15 | 82750362 | 82811069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759440 | C | T | 1 | a0003 | 21 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
missense_variant | MODERATE | c.2158G>A | p.Glu720Lys | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2340/6418 | 2158/2250 | 720/749 | chr15 | 82759440 | |||
chr15:82762238 | G | A | 1 | a0004 | 2 | HG02922.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1861C>T | p.His621Tyr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/13 | 2043/6418 | 1861/2250 | 621/749 | chr15 | 82762238 | |||
chr15:82765907 | G | A | 1 | a0005 | 2 | HG03471.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.1678C>T | p.His560Tyr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1860/6418 | 1678/2250 | 560/749 | chr15 | 82765907 | |||
chr15:82765945 | A | G | 1 | a0006 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1640T>C | p.Met547Thr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1822/6418 | 1640/2250 | 547/749 | chr15 | 82765945 | |||
chr15:82769022 | G | A | 1 | a0008 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1411C>T | p.Pro471Ser | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/13 | 1593/6418 | 1411/2250 | 471/749 | chr15 | 82769022 | |||
chr15:82772084 | G | A | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1256C>T | p.Thr419Met | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/13 | 1438/6418 | 1256/2250 | 419/749 | chr15 | 82772084 | |||
chr15:82778879 | T | G | 5 | a0002 a0006 a0007 others(2): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
missense_variant | MODERATE | c.998A>C | p.Lys333Thr | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/13 | 1180/6418 | 998/2250 | 333/749 | chr15 | 82778879 | |||
chr15:82782857 | A | AAGTATCT others(13): Show |
1 | a0009 | 1 | NA19081.hp2 | frameshift_variant&stop_gained | HIGH | c.884_903dupGTGGAGAA others(12): Show |
p.Cys302fs | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 1085/6418 | 903/2250 | 301/749 | chr15 | 82782857 | |||
chr15:82787093 | C | T | 1 | a0010 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.298G>A | p.Val100Ile | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/13 | 480/6418 | 298/2250 | 100/749 | chr15 | 82787093 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759441 | G | A | 3 | a0001c0002 a0001c0012 a0004c0006 |
95 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
synonymous_variant | LOW | c.2157C>T | p.His719His | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2339/6418 | 2157/2250 | 719/749 | chr15 | 82759441 | |||
chr15:82765956 | T | G | 1 | a0001c0012 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.1629A>C | p.Arg543Arg | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/13 | 1811/6418 | 1629/2250 | 543/749 | chr15 | 82765956 | |||
chr15:82778842 | T | C | 1 | a0001c0008 | 2 | HG01884.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.1035A>G | p.Ala345Ala | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/13 | 1217/6418 | 1035/2250 | 345/749 | chr15 | 82778842 | |||
chr15:82782807 | C | T | 1 | a0001c0011 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.954G>A | p.Val318Val | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 1136/6418 | 954/2250 | 318/749 | chr15 | 82782807 | |||
chr15:82782948 | C | T | 1 | a0004c0006 | 2 | HG02922.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.813G>A | p.Glu271Glu | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/13 | 995/6418 | 813/2250 | 271/749 | chr15 | 82782948 | |||
chr15:82786989 | G | A | 1 | a0001c0005 | 5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
synonymous_variant | LOW | c.402C>T | p.Phe134Phe | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/13 | 584/6418 | 402/2250 | 134/749 | chr15 | 82786989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82755506 | A | G | 1 | a0002c0003t0019 | 3 | HG02071.hp1 NA19002.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3842T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3842 | chr15 | 82755506 | ||||||
chr15:82755563 | A | AT | 5 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0048 others(2): Show |
12 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3784dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3784 | chr15 | 82755563 | ||||||
chr15:82755563 | AT | A | 10 | a0001c0001t0008 a0001c0001t0021 a0001c0001t0028 others(7): Show |
22 | HG00323.hp2 HG01070.hp2 HG02055.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3784delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3784 | chr15 | 82755563 | ||||||
chr15:82755944 | T | C | 2 | a0001c0001t0013 a0001c0001t0043 |
7 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3404A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3404 | chr15 | 82755944 | ||||||
chr15:82756281 | C | T | 1 | a0001c0001t0060 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3067G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 3067 | chr15 | 82756281 | ||||||
chr15:82756396 | TAAG | T | 15 | a0001c0001t0026 a0001c0002t0001 a0001c0002t0007 others(12): Show |
97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2949_*2951delCTT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2949 | chr15 | 82756396 | ||||||
chr15:82756562 | T | G | 3 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0056 |
20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2786 | chr15 | 82756562 | ||||||
chr15:82756567 | G | A | 1 | a0001c0002t0057 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2781C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2781 | chr15 | 82756567 | ||||||
chr15:82756673 | T | A | 2 | a0001c0001t0010 a0001c0001t0028 |
9 | NA18966.hp1 NA18981.hp2 NA18983.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2675A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2675 | chr15 | 82756673 | ||||||
chr15:82757118 | A | C | 2 | a0001c0001t0008 a0001c0011t0008 |
9 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2230T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2230 | chr15 | 82757118 | ||||||
chr15:82757210 | G | A | 1 | a0001c0001t0017 | 3 | HG03098.hp1 HG03209.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2138C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2138 | chr15 | 82757210 | ||||||
chr15:82757254 | A | C | 1 | a0003c0004t0046 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2094T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 2094 | chr15 | 82757254 | ||||||
chr15:82757351 | C | CT | 23 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(20): Show |
131 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1996dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | ||||||
chr15:82757351 | C | CTT | 4 | a0001c0001t0056 a0001c0002t0022 a0001c0002t0055 others(1): Show |
6 | HG01109.hp1 HG01952.hp1 HG04184.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1995_*1996dupAA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | ||||||
chr15:82757351 | CT | C | 32 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(29): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1996delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1996 | chr15 | 82757351 | ||||||
chr15:82757457 | G | A | 1 | a0001c0001t0044 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1891 | chr15 | 82757457 | ||||||
chr15:82757477 | G | A | 1 | a0002c0003t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1871C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1871 | chr15 | 82757477 | ||||||
chr15:82757480 | C | T | 1 | a0002c0003t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1868G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1868 | chr15 | 82757480 | ||||||
chr15:82757483 | C | T | 3 | a0001c0002t0007 a0001c0002t0034 a0001c0002t0054 |
13 | HG00423.hp1 HG00673.hp1 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1865G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1865 | chr15 | 82757483 | ||||||
chr15:82757498 | A | AT | 8 | a0001c0001t0031 a0003c0004t0006 a0003c0004t0020 others(5): Show |
21 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1849dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1849 | chr15 | 82757498 | ||||||
chr15:82757504 | T | TA | 1 | a0001c0001t0015 | 4 | HG02257.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1843_*1844insT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1843 | chr15 | 82757504 | ||||||
chr15:82757534 | G | A | 1 | a0003c0004t0050 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1814C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1814 | chr15 | 82757534 | ||||||
chr15:82757589 | C | T | 2 | a0003c0004t0020 a0003c0004t0045 |
4 | HG00741.hp1 HG01074.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1759 | chr15 | 82757589 | ||||||
chr15:82757590 | C | G | 2 | a0001c0001t0036 a0001c0002t0053 |
2 | NA18991.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1758G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1758 | chr15 | 82757590 | ||||||
chr15:82757628 | G | A | 2 | a0001c0002t0058 a0001c0002t0059 |
2 | NA18947.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1720C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1720 | chr15 | 82757628 | ||||||
chr15:82757767 | G | A | 1 | a0005c0007t0033 | 2 | HG03471.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1581C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1581 | chr15 | 82757767 | ||||||
chr15:82757858 | T | C | 1 | a0001c0001t0052 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1490A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1490 | chr15 | 82757858 | ||||||
chr15:82757893 | T | C | 27 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0013 others(24): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1455A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1455 | chr15 | 82757893 | ||||||
chr15:82757975 | A | G | 6 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0030 others(3): Show |
16 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1373T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1373 | chr15 | 82757975 | ||||||
chr15:82758027 | A | G | 1 | a0001c0001t0014 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1321 | chr15 | 82758027 | ||||||
chr15:82758047 | T | A | 1 | a0001c0001t0060 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1301 | chr15 | 82758047 | ||||||
chr15:82758050 | C | T | 1 | a0001c0001t0014 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1298G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1298 | chr15 | 82758050 | ||||||
chr15:82758070 | C | T | 4 | a0001c0001t0012 a0002c0003t0012 a0002c0003t0038 others(1): Show |
8 | HG00280.hp1 HG01975.hp1 HG02132.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1278G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1278 | chr15 | 82758070 | ||||||
chr15:82758080 | T | C | 1 | a0001c0002t0061 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1268 | chr15 | 82758080 | ||||||
chr15:82758099 | C | T | 1 | a0001c0001t0042 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1249G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1249 | chr15 | 82758099 | ||||||
chr15:82758191 | A | T | 2 | a0001c0001t0025 a0001c0001t0035 |
4 | NA18982.hp1 NA19001.hp2 NA19009.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1157 | chr15 | 82758191 | ||||||
chr15:82758268 | A | G | 13 | a0001c0001t0012 a0002c0003t0004 a0002c0003t0012 others(10): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1080T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 1080 | chr15 | 82758268 | ||||||
chr15:82758353 | C | T | 1 | a0002c0003t0038 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*995G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 995 | chr15 | 82758353 | ||||||
chr15:82758479 | A | C | 2 | a0001c0001t0008 a0001c0011t0008 |
9 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*869T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 869 | chr15 | 82758479 | ||||||
chr15:82758642 | T | C | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0017 others(9): Show |
80 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*706A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 706 | chr15 | 82758642 | ||||||
chr15:82758709 | A | G | 1 | a0001c0001t0030 | 2 | HG03486.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*639T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 639 | chr15 | 82758709 | ||||||
chr15:82758932 | C | T | 12 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0017 others(9): Show |
80 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*416G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 416 | chr15 | 82758932 | ||||||
chr15:82759066 | G | A | 1 | a0001c0001t0035 | 2 | NA19001.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*282C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 13/13 | 282 | chr15 | 82759066 | ||||||
chr15:82806030 | T | C | 1 | a0001c0001t0024 | 3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
5_prime_UTR_variant | MODIFIER | c.-143A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/13 | 18640 | chr15 | 82806030 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:82759689 | C | T | 1 | a0002c0003t0004g0368 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1998-89G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759689 | |||||||
chr15:82759738 | CATTTCTA others(5): Show |
C | 2 | a0001c0001t0002g0306 a0001c0001t0002g0307 |
2 | HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1998-150_1998-139d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759738 | |||||||
chr15:82759800 | C | CT | 36 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(33): Show |
37 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1998-201dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759800 | |||||||
chr15:82759816 | T | C | 324 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0120 others(321): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1998-216A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759816 | |||||||
chr15:82759960 | A | AT | 57 | a0001c0001t0012g0228 a0002c0003t0004g0005 a0002c0003t0004g0082 others(54): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1998-361dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759960 | |||||||
chr15:82759990 | C | T | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1998-390G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82759990 | |||||||
chr15:82760090 | G | A | 1 | a0001c0001t0044g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1998-490C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760090 | |||||||
chr15:82760103 | T | C | 3 | a0001c0001t0024g0373 a0001c0001t0024g0374 a0001c0001t0024g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1998-503A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760103 | |||||||
chr15:82760173 | T | G | 57 | a0001c0001t0012g0228 a0002c0003t0004g0005 a0002c0003t0004g0082 others(54): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1998-573A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760173 | |||||||
chr15:82760391 | A | T | 1 | a0001c0002t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1998-791T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760391 | |||||||
chr15:82760592 | C | CTA | 325 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0120 others(322): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1998-994_1998-993d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760592 | |||||||
chr15:82760723 | A | G | 325 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0120 others(322): Show |
332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1998-1123T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760723 | |||||||
chr15:82760739 | G | GCA | 217 | a0001c0001t0002g0120 a0001c0001t0002g0293 a0001c0001t0002g0318 others(214): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1998-1141_1998-114 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | |||||||
chr15:82760739 | G | GCACA | 79 | a0001c0001t0003g0179 a0001c0001t0003g0186 a0001c0001t0003g0199 others(76): Show |
80 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1998-1143_1998-114 others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | |||||||
chr15:82760739 | G | GCACACA | 6 | a0001c0001t0013g0165 a0001c0001t0013g0173 a0001c0001t0013g0175 others(3): Show |
6 | HG02965.hp2 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1998-1145_1998-114 others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | |||||||
chr15:82760739 | GCA | G | 5 | a0001c0001t0014g0001 a0001c0005t0011g0006 a0001c0005t0011g0370 others(2): Show |
9 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1998-1141_1998-114 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82760739 | |||||||
chr15:82761024 | T | C | 2 | a0003c0004t0006g0131 a0003c0004t0006g0132 |
2 | HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1997+1078A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761024 | |||||||
chr15:82761103 | G | A | 2 | a0001c0001t0013g0175 a0001c0001t0013g0322 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1997+999C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761103 | |||||||
chr15:82761357 | T | C | 1 | a0001c0002t0001g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1997+745A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761357 | |||||||
chr15:82761644 | T | C | 91 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0012 others(88): Show |
92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1997+458A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761644 | |||||||
chr15:82761659 | A | C | 6 | a0001c0001t0003g0166 a0001c0001t0003g0259 a0001c0001t0003g0260 others(3): Show |
6 | HG02451.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1997+443T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761659 | |||||||
chr15:82761688 | T | A | 66 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0012g0228 others(63): Show |
67 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1997+414A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761688 | |||||||
chr15:82761738 | A | G | 1 | a0001c0001t0044g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1997+364T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761738 | |||||||
chr15:82761921 | G | C | 61 | a0001c0001t0012g0228 a0001c0005t0011g0006 a0001c0005t0011g0370 others(58): Show |
63 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1997+181C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 12/12 | chr15 | 82761921 | |||||||
chr15:82762520 | A | G | 57 | a0001c0001t0012g0228 a0002c0003t0004g0005 a0002c0003t0004g0082 others(54): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821-242T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762520 | |||||||
chr15:82762700 | A | G | 67 | a0001c0001t0012g0228 a0001c0002t0001g0036 a0001c0002t0001g0072 others(64): Show |
69 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1821-422T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762700 | |||||||
chr15:82762907 | C | T | 3 | a0001c0001t0002g0086 a0001c0001t0002g0270 a0001c0001t0002g0308 |
3 | HG01952.hp2 HG02735.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1821-629G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762907 | |||||||
chr15:82762972 | A | G | 1 | a0002c0003t0004g0363 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1821-694T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82762972 | |||||||
chr15:82763153 | T | A | 57 | a0001c0001t0012g0228 a0002c0003t0004g0005 a0002c0003t0004g0082 others(54): Show |
58 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1821-875A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763153 | |||||||
chr15:82763321 | T | C | 1 | a0002c0003t0004g0348 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1821-1043A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763321 | |||||||
chr15:82763415 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1821-1137T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763415 | |||||||
chr15:82763675 | C | CTT | 198 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(195): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1821-1398_1821-139 others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763675 | |||||||
chr15:82763677 | G | C | 1 | a0001c0001t0002g0308 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1821-1399C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763677 | |||||||
chr15:82763897 | G | A | 10 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0213 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+1269C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763897 | |||||||
chr15:82763942 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1820+1224C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82763942 | |||||||
chr15:82764449 | G | A | 3 | a0001c0001t0008g0212 a0001c0001t0008g0213 a0001c0001t0008g0238 |
3 | HG02055.hp1 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1820+717C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764449 | |||||||
chr15:82764462 | C | T | 13 | a0003c0004t0006g0004 a0003c0004t0006g0009 a0003c0004t0006g0125 others(10): Show |
14 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1820+704G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764462 | |||||||
chr15:82764492 | C | CT | 15 | a0001c0001t0002g0035 a0001c0001t0002g0086 a0001c0001t0002g0294 others(12): Show |
16 | HG00323.hp1 HG00597.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1820+673dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTT | 7 | a0001c0001t0015g0217 a0001c0001t0015g0218 a0001c0001t0015g0219 others(4): Show |
7 | HG01243.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+672_1820+673d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(2): Show |
6 | a0002c0003t0004g0333 a0002c0003t0004g0337 a0002c0003t0004g0341 others(3): Show |
6 | HG01975.hp1 HG01993.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+665_1820+673d others(11): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(3): Show |
34 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(31): Show |
35 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1820+664_1820+673d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(4): Show |
13 | a0001c0001t0012g0228 a0002c0003t0004g0168 a0002c0003t0004g0224 others(10): Show |
13 | HG00423.hp2 HG01175.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1820+663_1820+673d others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(5): Show |
6 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0043g0163 others(3): Show |
6 | HG02895.hp1 HG03139.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+662_1820+673d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(8): Show |
1 | a0002c0003t0041g0362 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1820+659_1820+673d others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(9): Show |
3 | a0001c0002t0001g0100 a0001c0002t0034g0033 a0001c0002t0057g0102 |
3 | HG03041.hp2 HG03453.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1820+658_1820+673d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(10): Show |
13 | a0001c0002t0001g0029 a0001c0002t0001g0036 a0001c0002t0001g0053 others(10): Show |
13 | HG01943.hp1 HG02074.hp2 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+657_1820+673d others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(11): Show |
25 | a0001c0001t0009g0022 a0001c0001t0030g0287 a0001c0001t0042g0032 others(22): Show |
25 | HG00639.hp1 HG00673.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1820+656_1820+673d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(12): Show |
21 | a0001c0001t0005g0016 a0001c0001t0005g0023 a0001c0001t0005g0119 others(18): Show |
21 | HG00140.hp1 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1820+655_1820+673d others(21): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(13): Show |
12 | a0001c0001t0005g0018 a0001c0001t0005g0024 a0001c0001t0005g0026 others(9): Show |
12 | HG00099.hp2 HG01346.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1820+654_1820+673d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0005g0015 a0001c0001t0009g0021 |
2 | HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1820+673_1820+674i others(23): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(16): Show |
1 | a0005c0007t0033g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(25): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0013g0280 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(28): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0013g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1820+673_1820+674i others(34): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764492 | CTTTT | C | 108 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(105): Show |
112 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1820+670_1820+673d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764492 | |||||||
chr15:82764767 | C | T | 1 | a0001c0001t0003g0179 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1820+399G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764767 | |||||||
chr15:82764815 | T | C | 2 | a0001c0008t0023g0284 a0001c0008t0023g0285 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1820+351A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764815 | |||||||
chr15:82764817 | G | T | 6 | a0001c0001t0015g0217 a0001c0001t0015g0218 a0001c0001t0015g0219 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+349C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764817 | |||||||
chr15:82764956 | C | A | 92 | a0001c0001t0002g0086 a0001c0002t0001g0003 a0001c0002t0001g0011 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1820+210G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82764956 | |||||||
chr15:82765026 | A | G | 134 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(131): Show |
135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1820+140T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 11/12 | chr15 | 82765026 | |||||||
chr15:82765443 | A | G | 1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1688-145T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765443 | |||||||
chr15:82765497 | C | A | 3 | a0001c0001t0024g0373 a0001c0001t0024g0374 a0001c0001t0024g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1688-199G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765497 | |||||||
chr15:82765658 | G | A | 198 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(195): Show |
201 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1687+240C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765658 | |||||||
chr15:82765749 | G | A | 137 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(134): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1687+149C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765749 | |||||||
chr15:82765834 | G | T | 1 | a0001c0012t0001g0063 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1687+64C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 10/12 | chr15 | 82765834 | |||||||
chr15:82766336 | A | C | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-305T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766336 | |||||||
chr15:82766394 | C | T | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1554-363G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766394 | |||||||
chr15:82766451 | C | T | 2 | a0005c0007t0033g0028 a0005c0007t0033g0047 |
2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1554-420G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766451 | |||||||
chr15:82766456 | A | G | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1554-425T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766456 | |||||||
chr15:82766512 | C | T | 6 | a0001c0002t0001g0050 a0001c0002t0001g0058 a0001c0002t0001g0064 others(3): Show |
6 | HG00140.hp1 HG00639.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1554-481G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766512 | |||||||
chr15:82766558 | A | T | 10 | a0001c0002t0001g0011 a0001c0002t0001g0076 a0001c0002t0001g0077 others(7): Show |
10 | HG00609.hp1 HG01975.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.1554-527T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766558 | |||||||
chr15:82766688 | A | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0112 a0001c0002t0001g0249 |
3 | HG01243.hp2 HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1554-657T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766688 | |||||||
chr15:82766738 | C | CA | 57 | a0001c0001t0003g0169 a0001c0001t0010g0193 a0001c0001t0012g0228 others(54): Show |
58 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1554-708dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766738 | |||||||
chr15:82766738 | CA | C | 99 | a0001c0001t0002g0086 a0001c0001t0002g0306 a0001c0001t0005g0016 others(96): Show |
100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1554-708delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766738 | |||||||
chr15:82766755 | A | G | 6 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0200 others(3): Show |
6 | HG00741.hp2 HG01069.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1554-724T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766755 | |||||||
chr15:82766821 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1554-790G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766821 | |||||||
chr15:82766915 | G | A | 1 | a0002c0003t0018g0356 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1554-884C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82766915 | |||||||
chr15:82767076 | G | A | 326 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(323): Show |
333 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1554-1045C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767076 | |||||||
chr15:82767235 | T | C | 197 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(194): Show |
200 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1554-1204A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767235 | |||||||
chr15:82767303 | A | T | 1 | a0001c0001t0002g0268 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1554-1272T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767303 | |||||||
chr15:82767458 | T | C | 2 | a0001c0008t0023g0284 a0001c0008t0023g0285 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1553+1422A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767458 | |||||||
chr15:82767497 | T | C | 1 | a0001c0002t0007g0042 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1553+1383A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767497 | |||||||
chr15:82767602 | C | A | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0292 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553+1278G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767602 | |||||||
chr15:82767830 | G | A | 3 | a0001c0001t0024g0373 a0001c0001t0024g0374 a0001c0001t0024g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1553+1050C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767830 | |||||||
chr15:82767928 | C | T | 1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1553+952G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767928 | |||||||
chr15:82767933 | C | T | 135 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(132): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1553+947G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82767933 | |||||||
chr15:82768465 | A | G | 1 | a0001c0002t0001g0036 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1553+415T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768465 | |||||||
chr15:82768483 | C | T | 1 | a0001c0001t0003g0327 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1553+397G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768483 | |||||||
chr15:82768594 | T | TTGAA | 121 | a0001c0001t0002g0120 a0001c0001t0002g0320 a0001c0001t0005g0015 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1553+282_1553+285d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768594 | |||||||
chr15:82768594 | T | TTGAATGA others(1): Show |
3 | a0001c0001t0005g0211 a0001c0002t0001g0075 a0001c0002t0001g0159 |
3 | HG03130.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1553+278_1553+285d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 9/12 | chr15 | 82768594 | |||||||
chr15:82769041 | G | C | 1 | a0001c0001t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1403-11C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769041 | |||||||
chr15:82769288 | G | A | 2 | a0002c0003t0004g0220 a0002c0003t0004g0339 |
2 | HG00544.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1403-258C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769288 | |||||||
chr15:82769415 | C | CA | 11 | a0001c0001t0003g0013 a0001c0001t0003g0167 a0001c0001t0003g0170 others(8): Show |
12 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1402+334dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769415 | |||||||
chr15:82769415 | CA | C | 102 | a0001c0001t0005g0016 a0001c0001t0005g0018 a0001c0001t0005g0023 others(99): Show |
104 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1402+334delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769415 | |||||||
chr15:82769504 | G | A | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402+246C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769504 | |||||||
chr15:82769565 | C | CA | 29 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0214 others(26): Show |
29 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1402+184dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769565 | |||||||
chr15:82769639 | G | A | 1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1402+111C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769639 | |||||||
chr15:82769693 | T | G | 1 | a0001c0001t0002g0120 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1402+57A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 8/12 | chr15 | 82769693 | |||||||
chr15:82769925 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1268-41C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82769925 | |||||||
chr15:82769951 | G | A | 1 | a0001c0001t0010g0193 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1268-67C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82769951 | |||||||
chr15:82770126 | G | T | 20 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(17): Show |
20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1268-242C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770126 | |||||||
chr15:82770181 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1268-297C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770181 | |||||||
chr15:82770275 | C | T | 2 | a0005c0007t0033g0028 a0005c0007t0033g0047 |
2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1268-391G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770275 | |||||||
chr15:82770325 | G | A | 3 | a0001c0001t0024g0373 a0001c0001t0024g0374 a0001c0001t0024g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1268-441C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770325 | |||||||
chr15:82770331 | T | C | 317 | a0001c0001t0002g0120 a0001c0001t0002g0171 a0001c0001t0002g0172 others(314): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1268-447A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770331 | |||||||
chr15:82770571 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1268-687G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770571 | |||||||
chr15:82770735 | T | TG | 91 | a0001c0002t0001g0003 a0001c0002t0001g0011 a0001c0002t0001g0012 others(88): Show |
92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1268-852dupC | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770735 | |||||||
chr15:82770752 | T | C | 1 | a0002c0003t0004g0326 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1268-868A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770752 | |||||||
chr15:82770767 | A | G | 317 | a0001c0001t0002g0120 a0001c0001t0002g0171 a0001c0001t0002g0172 others(314): Show |
324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1268-883T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770767 | |||||||
chr15:82770904 | A | G | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1268-1020T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770904 | |||||||
chr15:82770928 | G | T | 2 | a0001c0001t0002g0296 a0001c0001t0002g0320 |
2 | HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1268-1044C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82770928 | |||||||
chr15:82771065 | C | T | 4 | a0001c0001t0003g0187 a0001c0001t0003g0190 a0001c0001t0003g0208 others(1): Show |
4 | NA18951.hp2 NA18975.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267+1008G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771065 | |||||||
chr15:82771263 | T | G | 2 | a0003c0004t0020g0221 a0003c0004t0045g0140 |
2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1267+810A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771263 | |||||||
chr15:82771274 | C | G | 195 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1267+799G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771274 | |||||||
chr15:82771592 | C | T | 195 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(192): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1267+481G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771592 | |||||||
chr15:82771735 | A | T | 135 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(132): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1267+338T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82771735 | |||||||
chr15:82772058 | C | T | 2 | a0001c0001t0002g0235 a0001c0001t0021g0210 |
2 | NA18964.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1267+15G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 7/12 | chr15 | 82772058 | |||||||
chr15:82772260 | C | A | 58 | a0001c0001t0003g0247 a0001c0001t0003g0261 a0002c0003t0004g0005 others(55): Show |
59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1112-32G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772260 | |||||||
chr15:82772297 | C | G | 2 | a0001c0001t0009g0020 a0001c0001t0009g0021 |
2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1112-69G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772297 | |||||||
chr15:82772313 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1112-85G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772313 | |||||||
chr15:82772356 | A | C | 1 | a0001c0002t0001g0053 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1112-128T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772356 | |||||||
chr15:82772389 | C | T | 1 | a0002c0003t0004g0352 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1112-161G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772389 | |||||||
chr15:82772417 | A | G | 1 | a0001c0001t0005g0015 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1112-189T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772417 | |||||||
chr15:82772551 | C | A | 1 | a0001c0001t0025g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1112-323G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772551 | |||||||
chr15:82772591 | C | G | 184 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0005g0015 others(181): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1112-363G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772591 | |||||||
chr15:82772752 | T | C | 1 | a0001c0001t0025g0227 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1112-524A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772752 | |||||||
chr15:82772761 | G | A | 2 | a0001c0001t0013g0175 a0001c0001t0013g0322 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1112-533C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82772761 | |||||||
chr15:82773047 | A | T | 1 | a0001c0001t0012g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1112-819T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773047 | |||||||
chr15:82773057 | C | T | 1 | a0002c0003t0018g0356 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1112-829G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773057 | |||||||
chr15:82773096 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1112-868G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773096 | |||||||
chr15:82773143 | C | T | 1 | a0002c0003t0004g0347 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1112-915G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773143 | |||||||
chr15:82773287 | T | A | 1 | a0001c0002t0054g0045 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1112-1059A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773287 | |||||||
chr15:82773289 | G | C | 12 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(9): Show |
12 | HG02717.hp1 HG02895.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1061C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773289 | |||||||
chr15:82773315 | G | A | 189 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(186): Show |
192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.1112-1087C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773315 | |||||||
chr15:82773439 | A | C | 10 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0213 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1112-1211T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773439 | |||||||
chr15:82773597 | A | G | 10 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0213 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1112-1369T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773597 | |||||||
chr15:82773701 | C | A | 1 | a0002c0003t0004g0082 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1112-1473G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82773701 | |||||||
chr15:82774247 | G | A | 1 | a0001c0001t0003g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1112-2019C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774247 | |||||||
chr15:82774365 | C | A | 2 | a0004c0006t0001g0098 a0004c0006t0001g0099 |
2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1112-2137G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774365 | |||||||
chr15:82774421 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1112-2193A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774421 | |||||||
chr15:82774616 | C | A | 1 | a0002c0003t0004g0338 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1112-2388G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774616 | |||||||
chr15:82774656 | C | A | 1 | a0001c0001t0002g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1112-2428G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774656 | |||||||
chr15:82774719 | C | CT | 9 | a0001c0001t0014g0001 a0001c0002t0001g0104 a0001c0008t0023g0284 others(6): Show |
12 | HG00323.hp2 HG00738.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-2492dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774719 | |||||||
chr15:82774791 | G | A | 2 | a0003c0004t0006g0152 a0003c0004t0006g0153 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1112-2563C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774791 | |||||||
chr15:82774847 | G | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112-2619C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82774847 | |||||||
chr15:82775039 | A | T | 1 | a0001c0001t0008g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1112-2811T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775039 | |||||||
chr15:82775089 | G | A | 55 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(52): Show |
56 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1112-2861C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775089 | |||||||
chr15:82775136 | C | T | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1112-2908G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775136 | |||||||
chr15:82775253 | C | T | 20 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0018 others(17): Show |
20 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1112-3025G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775253 | |||||||
chr15:82775331 | G | A | 1 | a0001c0001t0044g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1112-3103C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775331 | |||||||
chr15:82775397 | C | CA | 47 | a0001c0001t0002g0086 a0001c0001t0003g0199 a0001c0001t0003g0205 others(44): Show |
48 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1112-3170dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775397 | |||||||
chr15:82775419 | A | G | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0043g0163 |
3 | HG02895.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-3191T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775419 | |||||||
chr15:82775938 | T | G | 1 | a0001c0002t0001g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1111+2828A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775938 | |||||||
chr15:82775968 | A | G | 1 | a0001c0001t0005g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1111+2798T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82775968 | |||||||
chr15:82776148 | A | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2618T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776148 | |||||||
chr15:82776198 | G | A | 4 | a0001c0001t0003g0180 a0001c0001t0003g0277 a0001c0001t0003g0299 others(1): Show |
4 | HG02132.hp1 HG02135.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+2568C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776198 | |||||||
chr15:82776327 | T | C | 4 | a0001c0002t0001g0054 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+2439A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776327 | |||||||
chr15:82776331 | A | C | 6 | a0001c0001t0005g0030 a0001c0001t0005g0118 a0001c0001t0005g0119 others(3): Show |
6 | HG01346.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111+2435T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776331 | |||||||
chr15:82776365 | C | T | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2401G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776365 | |||||||
chr15:82776586 | C | T | 131 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(128): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1111+2180G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776586 | |||||||
chr15:82776631 | GA | G | 11 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(8): Show |
11 | HG02602.hp2 HG02698.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+2134delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776631 | |||||||
chr15:82776674 | C | A | 1 | a0005c0007t0033g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1111+2092G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82776674 | |||||||
chr15:82777113 | A | G | 3 | a0002c0003t0012g0329 a0002c0003t0012g0336 a0002c0003t0039g0323 |
3 | NA18953.hp2 NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1111+1653T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777113 | |||||||
chr15:82777276 | A | C | 3 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 |
3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1111+1490T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777276 | |||||||
chr15:82777555 | G | C | 9 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(6): Show |
9 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+1211C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777555 | |||||||
chr15:82777850 | T | TA | 22 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0005g0015 others(19): Show |
22 | HG00099.hp2 HG01069.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1111+915dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777850 | |||||||
chr15:82777936 | T | C | 1 | a0001c0001t0035g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+830A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777936 | |||||||
chr15:82777973 | C | T | 56 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(53): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1111+793G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82777973 | |||||||
chr15:82778011 | C | G | 1 | a0001c0001t0008g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111+755G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778011 | |||||||
chr15:82778127 | C | CAT | 27 | a0001c0001t0002g0127 a0001c0001t0002g0137 a0001c0001t0002g0147 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1111+637_1111+638d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATAT | 23 | a0001c0001t0002g0126 a0001c0001t0002g0291 a0001c0001t0002g0314 others(20): Show |
25 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1111+635_1111+638d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATAT | 39 | a0001c0001t0003g0014 a0001c0001t0003g0167 a0001c0001t0003g0169 others(36): Show |
39 | HG00140.hp1 HG00609.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1111+633_1111+638d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(1): Show |
48 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0003g0013 others(45): Show |
48 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1111+631_1111+638d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(3): Show |
23 | a0001c0001t0003g0087 a0001c0001t0003g0178 a0001c0001t0003g0181 others(20): Show |
23 | HG00544.hp2 HG00738.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1111+629_1111+638d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(5): Show |
21 | a0001c0001t0003g0174 a0001c0001t0003g0185 a0001c0001t0003g0207 others(18): Show |
21 | HG00597.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1111+627_1111+638d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(7): Show |
13 | a0001c0001t0002g0120 a0001c0001t0003g0209 a0001c0001t0010g0194 others(10): Show |
16 | HG00609.hp2 HG01891.hp2 HG02273.hp1 others(13): Show |
intron_variant | MODIFIER | c.1111+625_1111+638d others(16): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(9): Show |
13 | a0001c0001t0003g0264 a0001c0001t0013g0175 a0001c0001t0013g0322 others(10): Show |
13 | HG00323.hp2 HG01074.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1111+623_1111+638d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(11): Show |
4 | a0001c0001t0013g0165 a0001c0001t0026g0250 a0001c0002t0001g0060 others(1): Show |
4 | HG02895.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+621_1111+638d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(13): Show |
5 | a0001c0001t0002g0301 a0001c0001t0015g0217 a0001c0001t0015g0218 others(2): Show |
5 | HG01515.hp2 HG02257.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+619_1111+638d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(15): Show |
5 | a0001c0001t0002g0268 a0001c0001t0024g0373 a0001c0001t0024g0374 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+617_1111+638d others(24): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(17): Show |
6 | a0001c0001t0003g0327 a0001c0001t0015g0219 a0001c0001t0027g0244 others(3): Show |
6 | HG01099.hp1 HG02896.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1111+615_1111+638d others(26): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | C | CATATATA others(23): Show |
2 | a0001c0001t0002g0086 a0003c0004t0032g0136 |
2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1111+609_1111+638d others(32): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | CAT | C | 62 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0292 others(59): Show |
63 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1111+637_1111+638d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | CATAT | C | 9 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0005g0283 others(6): Show |
9 | HG01346.hp2 HG01361.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+635_1111+638d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778127 | CATATAT | C | 8 | a0001c0001t0023g0008 a0001c0002t0001g0096 a0001c0005t0011g0006 others(5): Show |
9 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.1111+633_1111+638d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778127 | |||||||
chr15:82778137 | T | TATATATA others(8): Show |
1 | a0001c0001t0003g0328 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1111+614_1111+628d others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778137 | |||||||
chr15:82778157 | T | TATAA | 3 | a0001c0001t0003g0166 a0001c0001t0017g0233 a0001c0001t0017g0265 |
3 | HG02818.hp2 HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1111+608_1111+609i others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778157 | |||||||
chr15:82778157 | T | TATATATA others(3): Show |
1 | a0001c0001t0003g0259 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+608_1111+609i others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778157 | |||||||
chr15:82778158 | A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1111+607_1111+608i others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | |||||||
chr15:82778158 | A | ATATATAT others(14): Show |
1 | a0001c0001t0008g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1111+607_1111+608i others(23): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | |||||||
chr15:82778158 | A | ATATATAT others(18): Show |
1 | a0001c0001t0008g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1111+607_1111+608i others(27): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | |||||||
chr15:82778158 | A | ATATATAT others(20): Show |
3 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0241 |
3 | HG02451.hp2 HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1111+607_1111+608i others(29): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | |||||||
chr15:82778158 | A | ATATATAT others(22): Show |
1 | a0001c0001t0008g0213 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1111+607_1111+608i others(31): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778158 | |||||||
chr15:82778467 | T | TA | 3 | a0001c0002t0001g0057 a0001c0002t0001g0090 a0001c0002t0016g0091 |
3 | HG02135.hp1 HG02523.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1111+298dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778467 | |||||||
chr15:82778479 | A | G | 1 | a0001c0001t0003g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1111+287T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778479 | |||||||
chr15:82778740 | C | T | 3 | a0001c0001t0024g0373 a0001c0001t0024g0374 a0001c0001t0024g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1111+26G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778740 | |||||||
chr15:82778742 | C | T | 1 | a0001c0001t0029g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1111+24G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 6/12 | chr15 | 82778742 | |||||||
chr15:82778919 | T | C | 3 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 |
3 | HG01884.hp2 HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.990-32A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82778919 | |||||||
chr15:82779036 | C | G | 56 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(53): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.990-149G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779036 | |||||||
chr15:82779337 | G | A | 2 | a0001c0001t0017g0234 a0001c0001t0017g0265 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.990-450C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779337 | |||||||
chr15:82779605 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.989+640C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779605 | |||||||
chr15:82779653 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.989+592G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779653 | |||||||
chr15:82779664 | C | CA | 25 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(22): Show |
25 | HG01109.hp1 HG01243.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.989+580dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779664 | |||||||
chr15:82779664 | CA | C | 9 | a0001c0001t0003g0174 a0001c0001t0003g0208 a0001c0001t0003g0230 others(6): Show |
9 | HG00597.hp2 HG01074.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.989+580delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779664 | |||||||
chr15:82779679 | A | G | 1 | a0001c0001t0005g0026 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.989+566T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779679 | |||||||
chr15:82779718 | C | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.989+527G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779718 | |||||||
chr15:82779738 | C | T | 188 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(185): Show |
191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.989+507G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779738 | |||||||
chr15:82779932 | T | C | 315 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(312): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.989+313A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82779932 | |||||||
chr15:82780226 | A | G | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.989+19T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 5/12 | chr15 | 82780226 | |||||||
chr15:82780278 | A | G | 5 | a0002c0003t0004g0334 a0002c0003t0004g0345 a0002c0003t0004g0348 others(2): Show |
5 | HG02083.hp1 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-11T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780278 | |||||||
chr15:82780337 | CT | C | 6 | a0001c0001t0025g0253 a0001c0002t0001g0059 a0001c0005t0011g0006 others(3): Show |
7 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.967-71delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780337 | |||||||
chr15:82780371 | GT | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.967-105delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780371 | |||||||
chr15:82780448 | C | T | 6 | a0001c0001t0015g0217 a0001c0001t0015g0218 a0001c0001t0015g0219 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-181G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780448 | |||||||
chr15:82780518 | A | T | 6 | a0001c0001t0003g0166 a0001c0001t0003g0259 a0001c0001t0003g0260 others(3): Show |
6 | HG02451.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-251T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780518 | |||||||
chr15:82780527 | G | A | 4 | a0001c0001t0023g0008 a0001c0005t0011g0370 a0001c0008t0023g0284 others(1): Show |
4 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.967-260C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780527 | |||||||
chr15:82780585 | G | A | 2 | a0002c0003t0004g0333 a0002c0003t0004g0337 |
2 | HG02015.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.967-318C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780585 | |||||||
chr15:82780627 | C | G | 6 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(3): Show |
6 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-360G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780627 | |||||||
chr15:82780704 | A | G | 1 | a0001c0002t0001g0282 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.967-437T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780704 | |||||||
chr15:82780867 | T | C | 1 | a0001c0001t0003g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.967-600A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780867 | |||||||
chr15:82780891 | C | T | 1 | a0001c0001t0052g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.967-624G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82780891 | |||||||
chr15:82781161 | G | A | 3 | a0001c0002t0001g0057 a0001c0002t0001g0090 a0001c0002t0016g0091 |
3 | HG02135.hp1 HG02523.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.967-894C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781161 | |||||||
chr15:82781161 | G | T | 2 | a0001c0001t0013g0175 a0001c0001t0013g0322 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.967-894C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781161 | |||||||
chr15:82781311 | G | A | 1 | a0001c0001t0013g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-1044C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781311 | |||||||
chr15:82781349 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.967-1082G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781349 | |||||||
chr15:82781613 | AATTAGGA others(10): Show |
A | 1 | a0001c0001t0010g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.966+1165_966+1181d others(19): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781613 | |||||||
chr15:82781638 | T | C | 6 | a0001c0001t0023g0008 a0001c0001t0042g0032 a0001c0008t0023g0284 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1157A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781638 | |||||||
chr15:82781649 | G | A | 6 | a0001c0001t0023g0008 a0001c0001t0042g0032 a0001c0008t0023g0284 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1146C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781649 | |||||||
chr15:82781674 | A | G | 6 | a0001c0002t0001g0053 a0001c0002t0001g0094 a0001c0002t0001g0096 others(3): Show |
6 | HG02074.hp2 NA18967.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1121T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781674 | |||||||
chr15:82781710 | T | C | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966+1085A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781710 | |||||||
chr15:82781773 | C | G | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.966+1022G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781773 | |||||||
chr15:82781787 | C | T | 2 | a0001c0001t0025g0227 a0001c0001t0025g0253 |
2 | NA18982.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.966+1008G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781787 | |||||||
chr15:82781941 | G | T | 3 | a0001c0001t0005g0030 a0001c0001t0005g0118 a0001c0001t0005g0119 |
3 | HG01346.hp2 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.966+854C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781941 | |||||||
chr15:82781969 | C | T | 3 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0154 |
3 | HG00323.hp1 HG01346.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.966+826G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781969 | |||||||
chr15:82781989 | G | A | 2 | a0001c0001t0013g0175 a0001c0001t0013g0322 |
2 | HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.966+806C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82781989 | |||||||
chr15:82782065 | A | AAAT | 26 | a0001c0001t0002g0046 a0001c0001t0002g0269 a0001c0001t0002g0305 others(23): Show |
26 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.966+727_966+729dup others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782065 | A | AAATAAT | 51 | a0001c0001t0002g0291 a0001c0001t0002g0304 a0001c0001t0005g0026 others(48): Show |
55 | HG00423.hp2 HG00544.hp1 HG01928.hp1 others(52): Show |
intron_variant | MODIFIER | c.966+724_966+729dup others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782065 | A | AAATAATA others(2): Show |
38 | a0001c0001t0002g0084 a0001c0001t0002g0289 a0001c0001t0002g0290 others(35): Show |
40 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.966+721_966+729dup others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782065 | A | AAATAATA others(5): Show |
18 | a0001c0001t0002g0083 a0001c0001t0002g0292 a0001c0001t0021g0312 others(15): Show |
18 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.966+718_966+729dup others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782065 | AAAT | A | 8 | a0001c0001t0003g0231 a0001c0001t0003g0259 a0001c0001t0003g0261 others(5): Show |
8 | HG00673.hp2 HG01361.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.966+727_966+729del others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782065 | AAATAAT | A | 87 | a0001c0001t0002g0120 a0001c0001t0002g0171 a0001c0001t0002g0172 others(84): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.966+724_966+729del others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782065 | |||||||
chr15:82782104 | T | A | 9 | a0001c0001t0002g0235 a0001c0001t0013g0164 a0001c0001t0013g0165 others(6): Show |
9 | HG01109.hp1 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+691A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAAA | 19 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(16): Show |
19 | HG00673.hp1 HG01346.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(2): Show |
28 | a0001c0001t0002g0040 a0001c0001t0002g0086 a0001c0001t0044g0162 others(25): Show |
29 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(5): Show |
1 | a0001c0001t0030g0286 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.966+690_966+691ins others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(5): Show |
33 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0029 others(30): Show |
33 | HG00323.hp1 HG00609.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(6): Show |
4 | a0001c0002t0001g0054 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(8): Show |
1 | a0001c0001t0030g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.966+690_966+691ins others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782104 | T | TAATAATA others(8): Show |
12 | a0001c0001t0060g0123 a0001c0002t0001g0036 a0001c0002t0001g0055 others(9): Show |
12 | HG01943.hp1 HG02280.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.966+690_966+691ins others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782104 | |||||||
chr15:82782111 | C | A | 3 | a0001c0002t0001g0240 a0001c0002t0001g0325 a0001c0002t0022g0223 |
3 | HG01109.hp1 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.966+684G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782111 | |||||||
chr15:82782171 | G | A | 9 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(6): Show |
9 | NA18964.hp1 NA18972.hp2 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+624C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782171 | |||||||
chr15:82782192 | A | G | 6 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(3): Show |
6 | HG02895.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+603T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782192 | |||||||
chr15:82782204 | G | A | 1 | a0001c0002t0054g0045 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.966+591C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782204 | |||||||
chr15:82782205 | C | G | 93 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(90): Show |
93 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.966+590G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782205 | |||||||
chr15:82782269 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.966+526C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782269 | |||||||
chr15:82782285 | A | G | 1 | a0002c0003t0004g0367 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.966+510T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782285 | |||||||
chr15:82782300 | T | C | 1 | a0001c0001t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.966+495A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782300 | |||||||
chr15:82782325 | A | G | 1 | a0001c0001t0002g0037 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.966+470T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782325 | |||||||
chr15:82782395 | G | A | 2 | a0001c0001t0002g0120 a0001c0001t0002g0268 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.966+400C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782395 | |||||||
chr15:82782417 | A | C | 110 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(107): Show |
112 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.966+378T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782417 | |||||||
chr15:82782436 | A | G | 2 | a0003c0004t0006g0131 a0003c0004t0006g0132 |
2 | HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.966+359T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782436 | |||||||
chr15:82782574 | C | T | 1 | a0001c0002t0034g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.966+221G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782574 | |||||||
chr15:82782609 | T | C | 164 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0214 others(161): Show |
165 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.966+186A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782609 | |||||||
chr15:82782615 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.966+180G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782615 | |||||||
chr15:82782645 | A | G | 1 | a0001c0001t0003g0209 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.966+150T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782645 | |||||||
chr15:82782731 | G | A | 3 | a0002c0003t0004g0348 a0002c0003t0004g0349 a0009c0010t0004g0350 |
3 | NA18975.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.966+64C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782731 | |||||||
chr15:82782763 | T | A | 1 | a0001c0001t0008g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.966+32A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 4/12 | chr15 | 82782763 | |||||||
chr15:82783297 | T | C | 324 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(321): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.736-272A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783297 | |||||||
chr15:82783342 | G | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-317C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783342 | |||||||
chr15:82783478 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.736-453C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783478 | |||||||
chr15:82783676 | A | C | 56 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(53): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.736-651T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783676 | |||||||
chr15:82783681 | G | C | 1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.736-656C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783681 | |||||||
chr15:82783759 | C | T | 1 | a0001c0001t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.736-734G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783759 | |||||||
chr15:82783859 | G | A | 1 | a0001c0001t0003g0328 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.736-834C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783859 | |||||||
chr15:82783859 | G | T | 3 | a0001c0002t0001g0097 a0001c0002t0001g0108 a0001c0002t0001g0160 |
3 | HG02074.hp2 NA19062.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.736-834C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783859 | |||||||
chr15:82783870 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.736-845G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82783870 | |||||||
chr15:82784056 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736-1031T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784056 | |||||||
chr15:82784114 | T | A | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1089A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784114 | |||||||
chr15:82784121 | G | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1096C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784121 | |||||||
chr15:82784124 | A | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1099T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784124 | |||||||
chr15:82784129 | G | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1104C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784129 | |||||||
chr15:82784133 | A | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1108T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784133 | |||||||
chr15:82784142 | C | G | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1117G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784142 | |||||||
chr15:82784143 | T | A | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1118A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784143 | |||||||
chr15:82784177 | G | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1152C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784177 | |||||||
chr15:82784182 | A | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1157T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784182 | |||||||
chr15:82784183 | A | T | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1158T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784183 | |||||||
chr15:82784185 | G | A | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1160C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784185 | |||||||
chr15:82784194 | T | G | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1169A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784194 | |||||||
chr15:82784206 | C | G | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1181G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784206 | |||||||
chr15:82784207 | T | C | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1182A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784207 | |||||||
chr15:82784208 | G | A | 1 | a0009c0010t0004g0350 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.736-1183C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784208 | |||||||
chr15:82784230 | T | TTTTTA | 125 | a0001c0001t0002g0086 a0001c0001t0003g0013 a0001c0001t0003g0014 others(122): Show |
126 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.736-1210_736-1206d others(7): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784230 | |||||||
chr15:82784230 | T | TTTTTATT others(3): Show |
3 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0022g0092 |
3 | HG01346.hp1 HG01952.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.736-1215_736-1206d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784230 | |||||||
chr15:82784250 | AT | A | 14 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0145 others(11): Show |
15 | HG00423.hp2 HG00735.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.736-1226delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784250 | |||||||
chr15:82784252 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.736-1227A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784252 | |||||||
chr15:82784254 | T | A | 47 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0175 others(44): Show |
47 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.736-1229A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784254 | |||||||
chr15:82784255 | A | T | 50 | a0001c0001t0002g0046 a0001c0001t0013g0164 a0001c0001t0013g0165 others(47): Show |
53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.736-1230T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784255 | |||||||
chr15:82784260 | T | A | 129 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(126): Show |
130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.736-1235A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784260 | |||||||
chr15:82784290 | G | A | 1 | a0001c0001t0005g0023 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.736-1265C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784290 | |||||||
chr15:82784492 | C | A | 2 | a0003c0004t0006g0177 a0003c0004t0032g0136 |
2 | HG01099.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.736-1467G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784492 | |||||||
chr15:82784527 | G | A | 1 | a0001c0002t0061g0109 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.736-1502C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784527 | |||||||
chr15:82784586 | C | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-1561G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784586 | |||||||
chr15:82784743 | A | G | 331 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(328): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.736-1718T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784743 | |||||||
chr15:82784844 | G | T | 1 | a0001c0001t0003g0186 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.735+1667C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784844 | |||||||
chr15:82784852 | C | G | 1 | a0001c0001t0003g0353 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.735+1659G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82784852 | |||||||
chr15:82785300 | A | ATTAT | 112 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0111 others(109): Show |
113 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.735+1207_735+1210d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | |||||||
chr15:82785300 | A | ATTATTTA others(1): Show |
25 | a0001c0001t0002g0086 a0001c0001t0003g0209 a0001c0001t0008g0212 others(22): Show |
25 | HG00609.hp2 HG01943.hp1 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.735+1203_735+1210d others(10): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | |||||||
chr15:82785300 | ATTAT | A | 13 | a0001c0001t0003g0166 a0001c0001t0003g0231 a0001c0001t0003g0260 others(10): Show |
16 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.735+1207_735+1210d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | |||||||
chr15:82785300 | ATTATTTA others(5): Show |
A | 8 | a0001c0001t0003g0205 a0001c0001t0003g0232 a0001c0001t0003g0255 others(5): Show |
8 | HG03471.hp1 HG03486.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+1199_735+1210d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785300 | |||||||
chr15:82785323 | AT | A | 18 | a0001c0001t0013g0280 a0003c0004t0006g0004 a0003c0004t0006g0009 others(15): Show |
19 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.735+1187delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785323 | |||||||
chr15:82785355 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0268 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.735+1156G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785355 | |||||||
chr15:82785436 | T | A | 2 | a0001c0001t0009g0010 a0001c0001t0009g0049 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.735+1075A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785436 | |||||||
chr15:82785530 | G | A | 56 | a0002c0003t0004g0005 a0002c0003t0004g0082 a0002c0003t0004g0110 others(53): Show |
57 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.735+981C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785530 | |||||||
chr15:82785601 | G | A | 1 | a0002c0003t0018g0356 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.735+910C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785601 | |||||||
chr15:82785613 | C | T | 5 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+898G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785613 | |||||||
chr15:82785700 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.735+811T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785700 | |||||||
chr15:82785772 | A | AC | 8 | a0001c0001t0002g0171 a0001c0001t0003g0252 a0001c0001t0010g0193 others(5): Show |
8 | HG00438.hp1 HG01109.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.735+738dupG | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785772 | |||||||
chr15:82785871 | G | A | 3 | a0001c0001t0026g0248 a0001c0001t0026g0250 a0001c0002t0001g0249 |
3 | HG01109.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.735+640C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82785871 | |||||||
chr15:82786385 | A | G | 189 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(186): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.735+126T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 3/12 | chr15 | 82786385 | |||||||
chr15:82786671 | G | A | 18 | a0001c0001t0013g0280 a0003c0004t0006g0004 a0003c0004t0006g0125 others(15): Show |
19 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.640-65C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/12 | chr15 | 82786671 | |||||||
chr15:82786716 | T | C | 1 | a0001c0001t0008g0243 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.639+36A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 2/12 | chr15 | 82786716 | |||||||
chr15:82787614 | A | AT | 8 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0214 others(5): Show |
8 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-147dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787614 | |||||||
chr15:82787618 | G | T | 8 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0214 others(5): Show |
8 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-150C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787618 | |||||||
chr15:82787663 | G | T | 1 | a0002c0003t0018g0344 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-78-195C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787663 | |||||||
chr15:82787720 | TA | T | 64 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(61): Show |
65 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-78-253delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787720 | |||||||
chr15:82787723 | A | G | 13 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0237 others(10): Show |
13 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-78-255T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82787723 | |||||||
chr15:82788056 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-78-588C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788056 | |||||||
chr15:82788221 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78-753G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788221 | |||||||
chr15:82788300 | G | A | 92 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-78-832C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788300 | |||||||
chr15:82788326 | T | C | 2 | a0001c0002t0001g0053 a0001c0002t0001g0094 |
2 | NA18967.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-78-858A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788326 | |||||||
chr15:82788341 | C | CA | 148 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(145): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-78-874dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | |||||||
chr15:82788341 | C | CAA | 11 | a0001c0001t0056g0121 a0001c0002t0001g0056 a0001c0002t0001g0057 others(8): Show |
11 | HG01517.hp2 HG02074.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78-875_-78-874dup others(2): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | |||||||
chr15:82788341 | CA | C | 58 | a0001c0001t0008g0141 a0001c0001t0013g0173 a0001c0001t0042g0032 others(55): Show |
59 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-78-874delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788341 | |||||||
chr15:82788491 | C | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-1023G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788491 | |||||||
chr15:82788494 | G | A | 1 | a0001c0002t0001g0154 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-78-1026C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788494 | |||||||
chr15:82788504 | C | CA | 8 | a0001c0001t0002g0137 a0001c0001t0002g0146 a0001c0001t0002g0148 others(5): Show |
8 | HG00099.hp1 HG00423.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-1037dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | |||||||
chr15:82788504 | CA | C | 278 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(275): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.-78-1037delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | |||||||
chr15:82788504 | CAA | C | 13 | a0001c0001t0003g0138 a0001c0001t0005g0030 a0001c0001t0010g0184 others(10): Show |
13 | HG00323.hp2 HG01069.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-1038_-78-1037d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788504 | |||||||
chr15:82788577 | A | T | 5 | a0001c0002t0001g0036 a0001c0002t0007g0034 a0001c0002t0007g0043 others(2): Show |
5 | NA18956.hp1 NA18957.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.-78-1109T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788577 | |||||||
chr15:82788672 | C | T | 190 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(187): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.-78-1204G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788672 | |||||||
chr15:82788977 | TA | T | 63 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(60): Show |
64 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.-78-1510delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82788977 | |||||||
chr15:82789057 | G | A | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-1589C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789057 | |||||||
chr15:82789354 | T | TATA | 37 | a0001c0001t0002g0046 a0001c0001t0002g0120 a0001c0001t0002g0147 others(34): Show |
38 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-78-1889_-78-1887d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | |||||||
chr15:82789354 | T | TATAATA | 39 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(36): Show |
39 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.-78-1892_-78-1887d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | |||||||
chr15:82789354 | T | TATAATAA others(2): Show |
40 | a0001c0001t0002g0039 a0001c0001t0013g0175 a0001c0001t0013g0322 others(37): Show |
41 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.-78-1895_-78-1887d others(11): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | |||||||
chr15:82789354 | T | TATAATAA others(5): Show |
13 | a0001c0001t0002g0086 a0001c0002t0001g0050 a0001c0002t0001g0057 others(10): Show |
13 | HG02080.hp2 HG02135.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-78-1898_-78-1887d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | |||||||
chr15:82789354 | TATA | T | 3 | a0001c0001t0002g0269 a0002c0003t0004g0363 a0005c0007t0033g0047 |
3 | HG02080.hp1 NA19043.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-78-1889_-78-1887d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789354 | |||||||
chr15:82789406 | A | T | 92 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-78-1938T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789406 | |||||||
chr15:82789459 | T | TACATTAT others(22): Show |
1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-78-2020_-78-1992d others(31): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789459 | |||||||
chr15:82789605 | T | A | 1 | a0008c0014t0004g0245 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-78-2137A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789605 | |||||||
chr15:82789613 | A | G | 124 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-78-2145T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789613 | |||||||
chr15:82789635 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-78-2167A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82789635 | |||||||
chr15:82790125 | A | G | 11 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(8): Show |
11 | HG02602.hp2 HG02698.hp2 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.-78-2657T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790125 | |||||||
chr15:82790188 | C | T | 1 | a0001c0001t0031g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-78-2720G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790188 | |||||||
chr15:82790189 | G | GACA | 20 | a0001c0001t0013g0280 a0003c0004t0006g0004 a0003c0004t0006g0125 others(17): Show |
21 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-78-2724_-78-2722d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | |||||||
chr15:82790189 | GACA | G | 183 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(180): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-78-2724_-78-2722d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | |||||||
chr15:82790189 | GACAACA | G | 7 | a0002c0003t0004g0335 a0002c0003t0004g0338 a0002c0003t0004g0340 others(4): Show |
7 | HG00423.hp2 HG02040.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.-78-2727_-78-2722d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790189 | |||||||
chr15:82790206 | CAACA | C | 6 | a0001c0001t0015g0217 a0001c0001t0015g0218 a0001c0001t0015g0219 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-2742_-78-2739d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790206 | |||||||
chr15:82790427 | C | T | 1 | a0003c0004t0032g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-78-2959G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790427 | |||||||
chr15:82790439 | C | G | 1 | a0003c0004t0006g0004 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-78-2971G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790439 | |||||||
chr15:82790544 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0009g0027 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-78-3077_-78-3076i others(15): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TGTGTGTG others(8): Show |
1 | a0001c0002t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-78-3077_-78-3076i others(17): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTG | 56 | a0001c0001t0002g0147 a0001c0001t0003g0353 a0001c0001t0010g0182 others(53): Show |
60 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-78-3078_-78-3077d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTG | 23 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(20): Show |
24 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-3080_-78-3077d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTG | 11 | a0001c0001t0013g0175 a0001c0001t0013g0322 a0001c0001t0023g0008 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-78-3082_-78-3077d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(3): Show |
6 | a0001c0002t0001g0003 a0001c0002t0001g0056 a0001c0002t0001g0088 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78-3086_-78-3077d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(5): Show |
27 | a0001c0001t0002g0086 a0001c0001t0005g0015 a0001c0001t0005g0016 others(24): Show |
27 | HG00099.hp2 HG01106.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-78-3088_-78-3077d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(7): Show |
54 | a0001c0001t0002g0111 a0001c0001t0009g0010 a0001c0001t0009g0049 others(51): Show |
54 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-78-3090_-78-3077d others(16): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(9): Show |
6 | a0001c0002t0001g0029 a0001c0002t0001g0050 a0001c0002t0001g0055 others(3): Show |
6 | HG01243.hp2 HG02083.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-78-3092_-78-3077d others(18): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(11): Show |
2 | a0004c0006t0001g0098 a0004c0006t0001g0099 |
2 | HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-78-3094_-78-3077d others(20): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790544 | T | TTGTGTGT others(13): Show |
1 | a0001c0002t0001g0057 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-78-3096_-78-3077d others(22): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790544 | |||||||
chr15:82790618 | T | C | 184 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(181): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-78-3150A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790618 | |||||||
chr15:82790629 | C | G | 2 | a0001c0005t0011g0370 a0001c0005t0011g0371 |
2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-78-3161G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790629 | |||||||
chr15:82790644 | C | T | 1 | a0005c0007t0033g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-78-3176G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790644 | |||||||
chr15:82790661 | C | T | 115 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(112): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-78-3193G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790661 | |||||||
chr15:82790662 | G | A | 1 | a0001c0002t0007g0271 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-78-3194C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790662 | |||||||
chr15:82790714 | T | C | 4 | a0001c0002t0001g0054 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3246A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790714 | |||||||
chr15:82790721 | G | A | 3 | a0001c0001t0013g0175 a0001c0001t0013g0322 a0005c0007t0033g0047 |
3 | HG02965.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-78-3253C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790721 | |||||||
chr15:82790742 | A | AT | 146 | a0001c0001t0002g0086 a0001c0001t0002g0111 a0001c0001t0002g0120 others(143): Show |
147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-78-3275dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790742 | |||||||
chr15:82790742 | A | ATT | 94 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(91): Show |
95 | HG00140.hp1 HG00323.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.-78-3276_-78-3275d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790742 | |||||||
chr15:82790809 | T | A | 2 | a0001c0001t0002g0086 a0001c0002t0016g0085 |
2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-78-3341A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790809 | |||||||
chr15:82790927 | G | T | 24 | a0001c0001t0003g0087 a0001c0001t0003g0183 a0001c0001t0003g0185 others(21): Show |
24 | HG00609.hp2 HG02015.hp1 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.-78-3459C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82790927 | |||||||
chr15:82791148 | G | A | 1 | a0001c0001t0029g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-78-3680C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791148 | |||||||
chr15:82791155 | T | A | 1 | a0001c0001t0029g0206 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-78-3687A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791155 | |||||||
chr15:82791155 | T | C | 1 | a0001c0001t0003g0261 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-78-3687A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791155 | |||||||
chr15:82791209 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-78-3741T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791209 | |||||||
chr15:82791241 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-78-3773C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791241 | |||||||
chr15:82791258 | A | G | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3790T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791258 | |||||||
chr15:82791288 | G | C | 4 | a0001c0002t0001g0036 a0001c0002t0007g0034 a0001c0002t0007g0043 others(1): Show |
4 | NA18956.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3820C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791288 | |||||||
chr15:82791289 | C | A | 4 | a0001c0002t0001g0036 a0001c0002t0007g0034 a0001c0002t0007g0043 others(1): Show |
4 | NA18956.hp1 NA18957.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-3821G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791289 | |||||||
chr15:82791378 | A | T | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-3910T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791378 | |||||||
chr15:82791430 | A | G | 330 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(327): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.-78-3962T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791430 | |||||||
chr15:82791651 | A | G | 1 | a0001c0008t0023g0284 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-78-4183T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791651 | |||||||
chr15:82791663 | C | T | 1 | a0003c0004t0046g0128 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-78-4195G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791663 | |||||||
chr15:82791732 | C | T | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-78-4264G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791732 | |||||||
chr15:82791929 | G | T | 3 | a0002c0003t0012g0329 a0002c0003t0012g0336 a0002c0003t0039g0323 |
3 | NA18953.hp2 NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-78-4461C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791929 | |||||||
chr15:82791945 | C | T | 52 | a0001c0001t0003g0353 a0001c0001t0013g0164 a0001c0001t0013g0165 others(49): Show |
53 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-78-4477G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82791945 | |||||||
chr15:82792119 | G | T | 4 | a0001c0002t0001g0054 a0001c0002t0001g0059 a0001c0002t0001g0060 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-4651C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792119 | |||||||
chr15:82792288 | G | A | 51 | a0001c0001t0003g0353 a0001c0001t0013g0164 a0001c0001t0013g0165 others(48): Show |
52 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-78-4820C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792288 | |||||||
chr15:82792491 | A | G | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-5023T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792491 | |||||||
chr15:82792509 | C | G | 190 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(187): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.-78-5041G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792509 | |||||||
chr15:82792780 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-78-5312C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792780 | |||||||
chr15:82792991 | A | G | 1 | a0001c0001t0002g0148 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-78-5523T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82792991 | |||||||
chr15:82793121 | G | A | 24 | a0001c0001t0002g0120 a0001c0001t0003g0013 a0001c0001t0003g0014 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-78-5653C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793121 | |||||||
chr15:82793142 | C | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-5674G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793142 | |||||||
chr15:82793164 | C | T | 20 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(17): Show |
21 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-78-5696G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793164 | |||||||
chr15:82793325 | G | GT | 7 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.-78-5858dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793325 | |||||||
chr15:82793325 | G | T | 1 | a0001c0001t0010g0182 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-78-5857C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793325 | |||||||
chr15:82793602 | T | C | 1 | a0002c0003t0012g0360 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-78-6134A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793602 | |||||||
chr15:82793712 | T | C | 1 | a0001c0001t0002g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-78-6244A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793712 | |||||||
chr15:82793759 | A | C | 1 | a0002c0003t0004g0145 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-78-6291T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793759 | |||||||
chr15:82793763 | A | G | 38 | a0001c0001t0003g0353 a0002c0003t0004g0005 a0002c0003t0004g0145 others(35): Show |
39 | HG00423.hp2 HG00544.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-78-6295T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82793763 | |||||||
chr15:82794031 | T | G | 16 | a0001c0001t0003g0087 a0001c0002t0001g0012 a0001c0002t0001g0056 others(13): Show |
16 | HG00408.hp2 HG01952.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-78-6563A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794031 | |||||||
chr15:82794048 | T | G | 1 | a0001c0002t0016g0116 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-78-6580A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794048 | |||||||
chr15:82794140 | C | G | 18 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(15): Show |
18 | HG02965.hp2 HG02976.hp2 NA18956.hp1 others(15): Show |
intron_variant | MODIFIER | c.-78-6672G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794140 | |||||||
chr15:82794141 | A | G | 16 | a0001c0001t0008g0141 a0001c0001t0008g0212 a0001c0001t0008g0213 others(13): Show |
16 | HG01109.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-78-6673T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794141 | |||||||
chr15:82794329 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-78-6861G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794329 | |||||||
chr15:82794341 | A | G | 132 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(129): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-78-6873T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794341 | |||||||
chr15:82794461 | G | C | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-6993C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794461 | |||||||
chr15:82794726 | CT | C | 9 | a0001c0001t0002g0035 a0001c0001t0002g0315 a0001c0001t0014g0001 others(6): Show |
12 | HG01099.hp1 HG02809.hp2 HG03139.hp1 others(9): Show |
intron_variant | MODIFIER | c.-78-7259delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794726 | |||||||
chr15:82794754 | T | G | 3 | a0001c0001t0003g0263 a0001c0001t0003g0264 a0001c0001t0037g0262 |
3 | HG01074.hp1 HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-78-7286A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794754 | |||||||
chr15:82794786 | G | A | 1 | a0001c0001t0012g0228 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-78-7318C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82794786 | |||||||
chr15:82795041 | T | C | 3 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 |
3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-78-7573A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795041 | |||||||
chr15:82795073 | C | T | 1 | a0001c0001t0044g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-78-7605G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795073 | |||||||
chr15:82795271 | T | C | 191 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(188): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.-78-7803A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795271 | |||||||
chr15:82795613 | T | G | 1 | a0001c0001t0002g0120 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-78-8145A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795613 | |||||||
chr15:82795620 | A | C | 24 | a0001c0001t0002g0120 a0001c0001t0003g0013 a0001c0001t0003g0014 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-78-8152T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795620 | |||||||
chr15:82795755 | C | A | 1 | a0001c0001t0030g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-78-8287G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795755 | |||||||
chr15:82795831 | C | CA | 57 | a0001c0001t0003g0353 a0001c0001t0013g0164 a0001c0001t0013g0165 others(54): Show |
59 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.-78-8364dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795831 | |||||||
chr15:82795842 | A | G | 2 | a0001c0001t0030g0286 a0001c0001t0030g0287 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-78-8374T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795842 | |||||||
chr15:82795860 | T | A | 332 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(329): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-78-8392A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82795860 | |||||||
chr15:82796000 | C | CT | 8 | a0001c0001t0002g0147 a0001c0001t0002g0294 a0001c0001t0002g0295 others(5): Show |
8 | HG00597.hp1 HG02602.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.-78-8533dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | |||||||
chr15:82796000 | CT | C | 136 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(133): Show |
139 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.-78-8533delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | |||||||
chr15:82796000 | CTT | C | 133 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(130): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-78-8534_-78-8533d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796000 | |||||||
chr15:82796007 | T | C | 8 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(5): Show |
8 | HG02895.hp1 HG03139.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-78-8539A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796007 | |||||||
chr15:82796088 | G | A | 1 | a0001c0001t0014g0001 | 4 | HG02809.hp2 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-78-8620C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796088 | |||||||
chr15:82796144 | G | A | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0207 |
3 | NA18947.hp2 NA18964.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-78-8676C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796144 | |||||||
chr15:82796228 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 |
3 | HG00140.hp2 HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-78-8760G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796228 | |||||||
chr15:82796276 | G | A | 1 | a0001c0001t0017g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-78-8808C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796276 | |||||||
chr15:82796296 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-78-8828G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796296 | |||||||
chr15:82796462 | C | T | 5 | a0001c0001t0017g0234 a0001c0002t0001g0054 a0001c0002t0001g0059 others(2): Show |
5 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-78-8994G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796462 | |||||||
chr15:82796479 | C | T | 22 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(19): Show |
23 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-78-9011G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796479 | |||||||
chr15:82796683 | T | C | 2 | a0001c0001t0002g0292 a0001c0001t0002g0293 |
2 | HG01175.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-78-9215A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796683 | |||||||
chr15:82796701 | C | G | 1 | a0001c0001t0003g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-78-9233G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82796701 | |||||||
chr15:82797006 | C | T | 80 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(77): Show |
81 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-79+8960G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797006 | |||||||
chr15:82797020 | T | TA | 7 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0009g0022 others(4): Show |
7 | HG00673.hp1 HG02004.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8945dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | |||||||
chr15:82797020 | TA | T | 118 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(115): Show |
122 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.-79+8945delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | |||||||
chr15:82797020 | TAA | T | 7 | a0001c0001t0002g0268 a0001c0001t0003g0183 a0001c0001t0003g0231 others(4): Show |
7 | HG02647.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8944_-79+8945d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797020 | |||||||
chr15:82797033 | A | AC | 108 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-79+8932_-79+8933i others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797033 | |||||||
chr15:82797033 | A | C | 1 | a0001c0002t0001g0058 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-79+8933T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797033 | |||||||
chr15:82797037 | A | AC | 23 | a0001c0001t0002g0120 a0001c0001t0003g0013 a0001c0001t0003g0014 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.-79+8928_-79+8929i others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797037 | |||||||
chr15:82797037 | A | C | 111 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(108): Show |
112 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-79+8929T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797037 | |||||||
chr15:82797040 | AAC | A | 7 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0013g0173 others(4): Show |
7 | HG02148.hp1 HG02895.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-79+8924_-79+8925d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797040 | |||||||
chr15:82797041 | AC | A | 44 | a0001c0001t0003g0353 a0002c0003t0004g0005 a0002c0003t0004g0145 others(41): Show |
45 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-79+8924delG | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797041 | |||||||
chr15:82797042 | C | A | 143 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(140): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.-79+8924G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797042 | |||||||
chr15:82797450 | A | G | 1 | a0001c0001t0005g0023 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-79+8516T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797450 | |||||||
chr15:82797536 | C | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0094 |
2 | NA18967.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-79+8430G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797536 | |||||||
chr15:82797592 | T | C | 329 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(326): Show |
336 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.-79+8374A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797592 | |||||||
chr15:82797679 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-79+8287C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797679 | |||||||
chr15:82797924 | T | C | 1 | a0001c0002t0016g0116 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-79+8042A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797924 | |||||||
chr15:82797942 | A | T | 1 | a0001c0001t0003g0230 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-79+8024T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797942 | |||||||
chr15:82797957 | C | T | 322 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(319): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.-79+8009G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82797957 | |||||||
chr15:82798343 | A | G | 194 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(191): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.-79+7623T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798343 | |||||||
chr15:82798509 | A | G | 3 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 |
3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+7457T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798509 | |||||||
chr15:82798737 | C | T | 2 | a0001c0002t0001g0029 a0005c0007t0033g0028 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+7229G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798737 | |||||||
chr15:82798865 | T | A | 52 | a0001c0001t0003g0353 a0001c0001t0013g0164 a0001c0001t0013g0165 others(49): Show |
53 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-79+7101A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798865 | |||||||
chr15:82798873 | G | GT | 61 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0039 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-79+7092dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | |||||||
chr15:82798873 | G | GTT | 81 | a0001c0001t0002g0035 a0001c0001t0003g0353 a0001c0001t0005g0023 others(78): Show |
83 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-79+7091_-79+7092d others(4): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | |||||||
chr15:82798873 | G | GTTT | 67 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0086 others(64): Show |
68 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-79+7090_-79+7092d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | |||||||
chr15:82798873 | G | GTTTT | 11 | a0001c0002t0001g0011 a0001c0002t0001g0054 a0001c0002t0001g0055 others(8): Show |
11 | HG01981.hp2 HG02055.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.-79+7089_-79+7092d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798873 | |||||||
chr15:82798877 | TG | T | 8 | a0001c0001t0002g0268 a0001c0001t0003g0201 a0001c0001t0003g0266 others(5): Show |
8 | HG01257.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-79+7088delC | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798877 | |||||||
chr15:82798878 | G | T | 324 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(321): Show |
331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.-79+7088C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82798878 | |||||||
chr15:82799034 | C | T | 131 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(128): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-79+6932G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799034 | |||||||
chr15:82799122 | C | T | 2 | a0001c0001t0002g0214 a0001c0002t0001g0050 |
2 | HG03704.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-79+6844G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799122 | |||||||
chr15:82799270 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-79+6696T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799270 | |||||||
chr15:82799581 | G | A | 1 | a0001c0002t0001g0104 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-79+6385C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799581 | |||||||
chr15:82799704 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-79+6262G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799704 | |||||||
chr15:82799903 | C | A | 135 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(132): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-79+6063G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799903 | |||||||
chr15:82799937 | C | T | 2 | a0001c0001t0008g0212 a0001c0001t0008g0213 |
2 | HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-79+6029G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82799937 | |||||||
chr15:82800061 | A | G | 24 | a0001c0001t0002g0120 a0001c0001t0003g0013 a0001c0001t0003g0014 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+5905T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800061 | |||||||
chr15:82800180 | C | T | 1 | a0001c0001t0021g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-79+5786G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800180 | |||||||
chr15:82800181 | T | C | 1 | a0001c0001t0010g0143 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-79+5785A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800181 | |||||||
chr15:82800538 | A | C | 1 | a0001c0001t0003g0013 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-79+5428T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800538 | |||||||
chr15:82800678 | C | G | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+5288G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800678 | |||||||
chr15:82800679 | G | A | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+5287C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800679 | |||||||
chr15:82800691 | C | CA | 11 | a0001c0001t0002g0137 a0001c0001t0002g0318 a0001c0001t0003g0277 others(8): Show |
11 | HG00423.hp1 HG02056.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.-79+5274dupT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAA | 33 | a0001c0001t0003g0353 a0002c0003t0004g0005 a0002c0003t0004g0279 others(30): Show |
34 | HG00280.hp1 HG00423.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-79+5272_-79+5274d others(5): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAA | 18 | a0001c0001t0013g0164 a0001c0001t0013g0173 a0001c0001t0013g0280 others(15): Show |
19 | HG00639.hp2 HG00735.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.-79+5271_-79+5274d others(6): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAA | 13 | a0001c0001t0013g0165 a0001c0001t0024g0373 a0001c0001t0024g0374 others(10): Show |
13 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-79+5270_-79+5274d others(7): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAAA | 78 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(75): Show |
79 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-79+5269_-79+5274d others(8): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAAAA | 24 | a0001c0001t0002g0046 a0001c0001t0002g0111 a0001c0001t0060g0123 others(21): Show |
24 | HG00408.hp1 HG00408.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-79+5268_-79+5274d others(9): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0120 a0001c0001t0005g0030 a0001c0001t0005g0118 others(2): Show |
5 | HG01346.hp2 HG01891.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+5265_-79+5274d others(12): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0005g0015 others(9): Show |
12 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-79+5264_-79+5274d others(13): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0003g0025 a0001c0001t0005g0023 a0001c0001t0005g0024 others(3): Show |
6 | HG01099.hp2 HG01106.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-79+5263_-79+5274d others(14): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82800691 | CA | C | 40 | a0001c0001t0002g0288 a0001c0001t0003g0138 a0001c0001t0003g0139 others(37): Show |
40 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.-79+5274delT | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82800691 | |||||||
chr15:82801017 | C | T | 2 | a0001c0001t0009g0010 a0001c0001t0009g0049 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-79+4949G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801017 | |||||||
chr15:82801308 | A | G | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+4658T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801308 | |||||||
chr15:82801354 | T | C | 1 | a0001c0001t0042g0032 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-79+4612A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801354 | |||||||
chr15:82801367 | C | T | 20 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(17): Show |
21 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-79+4599G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801367 | |||||||
chr15:82801497 | C | A | 1 | a0003c0004t0011g0031 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-79+4469G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801497 | |||||||
chr15:82801498 | C | T | 1 | a0003c0004t0011g0031 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-79+4468G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801498 | |||||||
chr15:82801573 | C | T | 2 | a0001c0002t0001g0029 a0005c0007t0033g0028 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+4393G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801573 | |||||||
chr15:82801940 | C | T | 18 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(15): Show |
18 | HG02965.hp2 HG02976.hp2 NA18956.hp1 others(15): Show |
intron_variant | MODIFIER | c.-79+4026G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82801940 | |||||||
chr15:82802178 | G | A | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3788C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802178 | |||||||
chr15:82802249 | C | G | 1 | a0001c0001t0003g0174 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-79+3717G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802249 | |||||||
chr15:82802332 | C | G | 1 | a0003c0004t0006g0152 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-79+3634G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802332 | |||||||
chr15:82802332 | C | T | 1 | a0001c0001t0013g0173 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-79+3634G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802332 | |||||||
chr15:82802497 | G | A | 1 | a0001c0002t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-79+3469C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802497 | |||||||
chr15:82802526 | A | G | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3440T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802526 | |||||||
chr15:82802539 | C | G | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0003g0169 others(1): Show |
4 | HG02109.hp1 HG03130.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+3427G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802539 | |||||||
chr15:82802747 | C | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+3219G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802747 | |||||||
chr15:82802907 | C | T | 1 | a0001c0002t0034g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-79+3059G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82802907 | |||||||
chr15:82803173 | T | A | 4 | a0001c0001t0023g0008 a0001c0008t0023g0284 a0001c0008t0023g0285 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-79+2793A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803173 | |||||||
chr15:82803240 | A | G | 1 | a0003c0004t0032g0124 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-79+2726T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803240 | |||||||
chr15:82803253 | C | T | 3 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 |
3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+2713G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803253 | |||||||
chr15:82803254 | G | A | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+2712C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803254 | |||||||
chr15:82803424 | T | C | 3 | a0001c0001t0030g0286 a0001c0001t0030g0287 a0001c0001t0044g0162 |
3 | HG03486.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-79+2542A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803424 | |||||||
chr15:82803597 | A | G | 334 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(331): Show |
341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.-79+2369T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803597 | |||||||
chr15:82803655 | G | C | 2 | a0003c0004t0006g0152 a0003c0004t0006g0153 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-79+2311C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803655 | |||||||
chr15:82803755 | T | C | 124 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-79+2211A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803755 | |||||||
chr15:82803861 | C | T | 1 | a0002c0003t0004g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-79+2105G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803861 | |||||||
chr15:82803990 | A | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+1976T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82803990 | |||||||
chr15:82804024 | A | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1942T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804024 | |||||||
chr15:82804026 | G | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1940C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804026 | |||||||
chr15:82804031 | A | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1935T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804031 | |||||||
chr15:82804032 | G | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1934C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804032 | |||||||
chr15:82804038 | G | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1928C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804038 | |||||||
chr15:82804043 | T | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1923A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804043 | |||||||
chr15:82804044 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1922C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804044 | |||||||
chr15:82804046 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1920A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804046 | |||||||
chr15:82804048 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1918A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804048 | |||||||
chr15:82804049 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1917A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804049 | |||||||
chr15:82804050 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1916C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804050 | |||||||
chr15:82804055 | T | A | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1911A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804055 | |||||||
chr15:82804063 | T | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1903A>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804063 | |||||||
chr15:82804070 | G | C | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1896C>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804070 | |||||||
chr15:82804075 | C | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1891G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804075 | |||||||
chr15:82804077 | A | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1889T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804077 | |||||||
chr15:82804078 | C | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1888G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804078 | |||||||
chr15:82804079 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1887G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804079 | |||||||
chr15:82804082 | A | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1884T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804082 | |||||||
chr15:82804087 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1879G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804087 | |||||||
chr15:82804093 | C | G | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1873G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804093 | |||||||
chr15:82804095 | T | A | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1871A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804095 | |||||||
chr15:82804096 | G | T | 1 | a0001c0001t0003g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-79+1870C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804096 | |||||||
chr15:82804217 | C | T | 1 | a0001c0001t0005g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-79+1749G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804217 | |||||||
chr15:82804237 | G | A | 1 | a0001c0001t0003g0319 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-79+1729C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804237 | |||||||
chr15:82804266 | C | T | 1 | a0001c0001t0005g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-79+1700G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804266 | |||||||
chr15:82804275 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-79+1691C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804275 | |||||||
chr15:82804305 | T | C | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+1661A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804305 | |||||||
chr15:82804513 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-79+1453G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804513 | |||||||
chr15:82804615 | C | A | 1 | a0001c0001t0060g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-79+1351G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804615 | |||||||
chr15:82804625 | C | T | 2 | a0001c0002t0001g0029 a0005c0007t0033g0028 |
2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-79+1341G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804625 | |||||||
chr15:82804790 | C | T | 3 | a0001c0001t0013g0164 a0001c0001t0013g0165 a0001c0001t0043g0163 |
3 | HG02895.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-79+1176G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804790 | |||||||
chr15:82804796 | C | T | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+1170G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804796 | |||||||
chr15:82804837 | A | G | 1 | a0001c0001t0027g0321 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-79+1129T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82804837 | |||||||
chr15:82805087 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+879T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805087 | |||||||
chr15:82805088 | G | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+878C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805088 | |||||||
chr15:82805089 | G | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+877C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805089 | |||||||
chr15:82805090 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+876G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805090 | |||||||
chr15:82805092 | T | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+874A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805092 | |||||||
chr15:82805100 | A | T | 1 | a0001c0001t0010g0197 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-79+866T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805100 | |||||||
chr15:82805104 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+862C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805104 | |||||||
chr15:82805106 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+860T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805106 | |||||||
chr15:82805108 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+858G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805108 | |||||||
chr15:82805109 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+857G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805109 | |||||||
chr15:82805110 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+856G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805110 | |||||||
chr15:82805112 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+854C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805112 | |||||||
chr15:82805113 | T | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+853A>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805113 | |||||||
chr15:82805114 | G | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+852C>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805114 | |||||||
chr15:82805115 | C | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+851G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805115 | |||||||
chr15:82805119 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+847T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805119 | |||||||
chr15:82805120 | C | G | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+846G>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805120 | |||||||
chr15:82805127 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+839T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805127 | |||||||
chr15:82805129 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+837C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805129 | |||||||
chr15:82805131 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+835G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805131 | |||||||
chr15:82805132 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+834G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805132 | |||||||
chr15:82805133 | C | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+833G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805133 | |||||||
chr15:82805134 | C | A | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+832G>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805134 | |||||||
chr15:82805135 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+831G>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805135 | |||||||
chr15:82805136 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+830T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805136 | |||||||
chr15:82805139 | A | C | 1 | a0001c0001t0044g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-79+827T>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805139 | |||||||
chr15:82805139 | A | T | 1 | a0001c0002t0001g0161 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-79+827T>A | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805139 | |||||||
chr15:82805140 | A | AT | 39 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0137 others(36): Show |
41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-79+825dupA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | |||||||
chr15:82805140 | A | ATT | 99 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0038 others(96): Show |
100 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-79+824_-79+825dup others(2): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | |||||||
chr15:82805140 | A | ATTT | 24 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0025 others(21): Show |
25 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-79+823_-79+825dup others(3): Show |
FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | |||||||
chr15:82805140 | AT | A | 48 | a0001c0001t0003g0327 a0001c0001t0003g0328 a0001c0001t0003g0353 others(45): Show |
48 | HG00280.hp1 HG00423.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-79+825delA | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805140 | |||||||
chr15:82805311 | G | A | 1 | a0002c0003t0004g0368 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-79+655C>T | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805311 | |||||||
chr15:82805714 | A | G | 1 | a0001c0001t0011g0007 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-79+252T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805714 | |||||||
chr15:82805860 | A | G | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+106T>C | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805860 | |||||||
chr15:82805889 | T | C | 4 | a0001c0005t0011g0006 a0001c0005t0011g0370 a0001c0005t0011g0371 others(1): Show |
5 | HG00639.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-79+77A>G | FSD2 | ENSG00000186628.12 | transcript | ENST00000334574.12 | protein_coding | 1/12 | chr15 | 82805889 |