Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5226 |
| ensemblid | ENSG00000142657.21 |
| hgncid | 8891 |
| symbol | PGD |
| name | phosphogluconate dehydrogenase |
| refseq_nuc | NM_002631.4 |
| refseq_prot | NP_002622.2 |
| ensembl_nuc | ENST00000270776.13 |
| ensembl_prot | ENSP00000270776.8 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 10399064 |
| end | 10420511 |
| strand | + |
| ver | v1.2 |
| region | chr1:10399064-10420511 |
| region5000 | chr1:10394064-10425511 |
| regionname0 | PGD_chr1_10399064_10420511 |
| regionname5000 | PGD_chr1_10394064_10425511 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 483 | 365 | 86 | 61 | 155 | 14 | 47 | 116 | PGD_chr1_10394064_10425511 | PGD | MAQAD others(478): Show |
chr1 | 10394064 | 10425511 |
| a0002 | 0/0 | 483 | 28 | 6 | 7 | 14 | 0 | 1 | 13 | PGD_chr1_10394064_10425511 | PGD | MAQAD others(478): Show |
chr1 | 10394064 | 10425511 |
| a0003 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | MAQAD others(478): Show |
chr1 | 10394064 | 10425511 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1449 | 224 | 48 | 38 | 94 | 10 | 32 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0002 | 0/0 | 1449 | 110 | 10 | 21 | 60 | 4 | 15 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0004 | 0/0 | 1449 | 21 | 20 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0006 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0007 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0008 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0010 | 0/0 | 1449 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0011 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0012 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0013 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0001c0014 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0002c0003 | 0/0 | 1449 | 23 | 6 | 7 | 9 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0002c0005 | 0/0 | 1449 | 5 | 0 | 0 | 5 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 | ||
| a0003c0009 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | ATGGC others(1444): Show |
chr1 | 10394064 | 10425511 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0002 | 0/0 | 2267 | 131 | 16 | 18 | 74 | 5 | 18 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0003 | 0/1 | 2266 | 51 | 25 | 7 | 7 | 3 | 8 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0004 | 1/0 | 2268 | 31 | 5 | 10 | 8 | 2 | 5 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2263): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0005 | 0/0 | 2267 | 3 | 1 | 2 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0009 | 0/0 | 2266 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0010 | 0/0 | 2266 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0011 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0012 | 0/0 | 2269 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2264): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0015 | 0/0 | 2255 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2250): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0017 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0001t0018 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2263): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0001 | 0/0 | 2265 | 101 | 9 | 20 | 55 | 4 | 13 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0003 | 0/0 | 2266 | 3 | 0 | 1 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0004 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2263): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0006 | 0/0 | 2265 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0007 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | CACTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0008 | 0/0 | 2265 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0002t0014 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0004t0001 | 0/0 | 2265 | 15 | 14 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0004t0003 | 0/0 | 2266 | 5 | 5 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0001c0004t0013 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0006t0002 | 0/0 | 2267 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0007t0001 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0008t0002 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0010t0016 | 0/0 | 2267 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0011t0002 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0012t0002 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2262): Show |
chr1 | 10394064 | 10425511 |
| a0001c0013t0001 | 0/0 | 2265 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0001c0014t0003 | 0/0 | 2266 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0002c0003t0001 | 0/0 | 2265 | 21 | 5 | 7 | 8 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0002c0003t0003 | 0/0 | 2266 | 2 | 1 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2261): Show |
chr1 | 10394064 | 10425511 |
| a0002c0005t0001 | 0/0 | 2265 | 5 | 0 | 0 | 5 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2260): Show |
chr1 | 10394064 | 10425511 |
| a0003c0009t0004 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | CCCTC others(2263): Show |
chr1 | 10394064 | 10425511 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0001 | 0/0 | 40 | 2 | 5 | 21 | 4 | 8 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0003 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0006 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0011 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0001 | 1/0 | 13 | 0 | 6 | 0 | 2 | 4 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0005g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0011g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0002 | 0/0 | 13 | 0 | 0 | 8 | 1 | 4 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0004 | 0/0 | 11 | 2 | 1 | 5 | 1 | 2 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0007g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0008g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0002t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0004t0013g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0006t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0007t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0008t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0010t0016g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0011t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0012t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0013t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0001c0014t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0007 | 0/0 | 7 | 1 | 5 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0009 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0003t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0002c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| a0003c0009t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | GBR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00423 | hp1 | a0002 | c0003 | t0001 | g0034 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00558 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00735 | hp2 | a0001 | c0010 | t0016 | g0139 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0119 | AMR | PUR | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0032 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0148 | EUR | IBS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | IBS | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0057 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0114 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02145 | hp1 | a0002 | c0003 | t0003 | g0060 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0113 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0023 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0061 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02523 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | KHV | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02602 | hp1 | a0001 | c0002 | t0007 | g0193 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0068 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0067 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02809 | hp2 | a0001 | c0012 | t0002 | g0196 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02818 | hp1 | a0001 | c0004 | t0001 | g0066 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02886 | hp2 | a0001 | c0002 | t0014 | g0084 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02896 | hp2 | a0001 | c0004 | t0003 | g0023 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02922 | hp2 | a0001 | c0006 | t0002 | g0025 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0122 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0118 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0117 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03098 | hp1 | a0001 | c0004 | t0003 | g0116 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03209 | hp2 | a0001 | c0006 | t0002 | g0025 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03486 | hp1 | a0001 | c0004 | t0013 | g0120 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03540 | hp1 | a0001 | c0014 | t0003 | g0029 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0124 | AFR | GWD | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0063 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03942 | hp1 | a0001 | c0002 | t0008 | g0111 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0001 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | STU | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | CHB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | CHB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18941 | hp1 | a0002 | c0005 | t0001 | g0058 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18952 | hp2 | a0003 | c0009 | t0004 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0034 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18972 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0026 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18977 | hp2 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18984 | hp2 | a0001 | c0001 | t0015 | g0052 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18994 | hp1 | a0002 | c0003 | t0003 | g0053 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19058 | hp2 | a0002 | c0005 | t0001 | g0062 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19060 | hp1 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19062 | hp2 | a0002 | c0005 | t0001 | g0054 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19067 | hp2 | a0001 | c0008 | t0002 | g0165 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19068 | hp2 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19070 | hp2 | a0002 | c0005 | t0001 | g0055 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19072 | hp1 | a0002 | c0005 | t0001 | g0056 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19240 | hp1 | a0001 | c0006 | t0002 | g0025 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | YRI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ASW | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ASW | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0185 | EUR | TSI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0073 | EUR | TSI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | GIH | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | CLM | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02109 | hp1 | a0001 | c0011 | t0002 | g0174 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02486 | hp2 | a0001 | c0007 | t0001 | g0064 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03471 | hp1 | a0001 | c0004 | t0003 | g0121 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | USA | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| HG06807 | hp2 | a0001 | c0013 | t0001 | g0106 | AFR | USA | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | USA | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0023 | AFR | USA | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | LWK | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0177 | REF | REF | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0001 | REF | REF | PGD_chr1_10394064_10425511 | PGD | chr1 | 10394064 | 10425511 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10413143 | G | A | 1 | a0002 | 28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
missense_variant | MODERATE | c.736G>A | p.Asp246Asn | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 790/2268 | 736/1452 | 246/483 | chr1 | 10413143 | |||
| chr1:10413209 | G | A | 1 | a0003 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.802G>A | p.Ala268Thr | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 856/2268 | 802/1452 | 268/483 | chr1 | 10413209 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10400428 | T | C | 2 | a0001c0002 a0001c0007 |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
synonymous_variant | LOW | c.120T>C | p.Asp40Asp | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/13 | 174/2268 | 120/1452 | 40/483 | chr1 | 10400428 | |||
| chr1:10400563 | C | T | 1 | a0001c0014 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.255C>T | p.Ile85Ile | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/13 | 309/2268 | 255/1452 | 85/483 | chr1 | 10400563 | |||
| chr1:10413124 | T | C | 1 | a0001c0008 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.717T>C | p.Ile239Ile | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 771/2268 | 717/1452 | 239/483 | chr1 | 10413124 | |||
| chr1:10413139 | C | T | 6 | a0001c0002 a0001c0004 a0001c0007 others(3): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
synonymous_variant | LOW | c.732C>T | p.Asp244Asp | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 786/2268 | 732/1452 | 244/483 | chr1 | 10413139 | |||
| chr1:10413142 | C | T | 1 | a0001c0006 | 3 | HG02922.hp2 HG03209.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.735C>T | p.Thr245Thr | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 789/2268 | 735/1452 | 245/483 | chr1 | 10413142 | |||
| chr1:10413181 | G | A | 1 | a0001c0013 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.774G>A | p.Ala258Ala | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/13 | 828/2268 | 774/1452 | 258/483 | chr1 | 10413181 | |||
| chr1:10417384 | C | T | 1 | a0001c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.984C>T | p.Tyr328Tyr | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/13 | 1038/2268 | 984/1452 | 328/483 | chr1 | 10417384 | |||
| chr1:10417441 | C | T | 1 | a0001c0011 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1041C>T | p.Thr347Thr | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/13 | 1095/2268 | 1041/1452 | 347/483 | chr1 | 10417441 | |||
| chr1:10417477 | C | G | 1 | a0001c0010 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1077C>G | p.Ala359Ala | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/13 | 1131/2268 | 1077/1452 | 359/483 | chr1 | 10417477 | |||
| chr1:10419734 | G | A | 2 | a0001c0007 a0002c0003 |
24 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(21): Show |
synonymous_variant | LOW | c.1437G>A | p.Ser479Ser | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 1491/2268 | 1437/1452 | 479/483 | chr1 | 10419734 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10399065 | C | A | 1 | a0001c0002t0007 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/13 | 53 | chr1 | 10399065 | ||||||
| chr1:10420019 | G | A | 1 | a0001c0002t0008 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*270G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 270 | chr1 | 10420019 | ||||||
| chr1:10420139 | G | C | 2 | a0001c0001t0005 a0001c0001t0009 |
4 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*390G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 390 | chr1 | 10420139 | ||||||
| chr1:10420198 | C | G | 1 | a0001c0002t0006 | 2 | HG00558.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 449 | chr1 | 10420198 | ||||||
| chr1:10420200 | T | C | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | NA18974.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 451 | chr1 | 10420200 | ||||||
| chr1:10420220 | T | TA | 3 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0012 |
5 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*480dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 481 | INFO_REALIGN_3_PRIME | chr1 | 10420220 | |||||
| chr1:10420222 | A | C | 1 | a0001c0002t0006 | 2 | HG00558.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*473A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 473 | chr1 | 10420222 | ||||||
| chr1:10420253 | C | T | 1 | a0001c0001t0018 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 504 | chr1 | 10420253 | ||||||
| chr1:10420254 | A | G | 1 | a0001c0001t0017 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 505 | chr1 | 10420254 | ||||||
| chr1:10420320 | G | C | 1 | a0001c0004t0013 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 571 | chr1 | 10420320 | ||||||
| chr1:10420370 | A | G | 1 | a0001c0010t0016 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 621 | chr1 | 10420370 | ||||||
| chr1:10420389 | CT | C | 8 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(5): Show |
140 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*664delT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 664 | INFO_REALIGN_3_PRIME | chr1 | 10420389 | |||||
| chr1:10420389 | CTT | C | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(4): Show |
65 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*663_*664delTT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 663 | INFO_REALIGN_3_PRIME | chr1 | 10420389 | |||||
| chr1:10420389 | CTTT | C | 13 | a0001c0001t0001 a0001c0001t0009 a0001c0002t0001 others(10): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*662_*664delTTT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 662 | INFO_REALIGN_3_PRIME | chr1 | 10420389 | |||||
| chr1:10420389 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0015 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*652_*664delTTTTTT others(7): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 652 | INFO_REALIGN_3_PRIME | chr1 | 10420389 | |||||
| chr1:10420394 | T | C | 1 | a0001c0002t0014 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*645T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 13/13 | 645 | chr1 | 10420394 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:10399175 | C | T | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.8+50C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399175 | |||||||
| chr1:10399214 | C | T | 3 | a0001c0001t0002g0195 a0001c0001t0003g0049 a0001c0012t0002g0196 |
4 | HG01167.hp1 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.8+89C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399214 | |||||||
| chr1:10399242 | C | A | 5 | a0001c0001t0002g0195 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
6 | HG01167.hp1 HG02145.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.8+117C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399242 | |||||||
| chr1:10399314 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.8+189C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399314 | |||||||
| chr1:10399345 | G | A | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 |
4 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.8+220G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399345 | |||||||
| chr1:10399349 | C | T | 1 | a0001c0002t0007g0193 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8+224C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399349 | |||||||
| chr1:10399389 | G | C | 1 | a0001c0001t0015g0052 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.9-240G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399389 | |||||||
| chr1:10399409 | G | A | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.9-220G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399409 | |||||||
| chr1:10399416 | G | A | 16 | a0001c0007t0001g0064 a0002c0003t0001g0007 a0002c0003t0001g0009 others(13): Show |
29 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.9-213G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399416 | |||||||
| chr1:10399599 | C | A | 1 | a0001c0002t0001g0065 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.9-30C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 1/12 | chr1 | 10399599 | |||||||
| chr1:10399722 | G | A | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.84+18G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399722 | |||||||
| chr1:10399740 | C | T | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.84+36C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399740 | |||||||
| chr1:10399754 | C | T | 3 | a0001c0004t0003g0023 a0001c0004t0003g0121 a0001c0004t0013g0120 |
5 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+50C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399754 | |||||||
| chr1:10399809 | T | C | 4 | a0001c0004t0001g0035 a0001c0004t0001g0066 a0001c0004t0001g0067 others(1): Show |
5 | HG02615.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+105T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399809 | |||||||
| chr1:10399882 | C | A | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.84+178C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399882 | |||||||
| chr1:10399901 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0003g0024 a0001c0001t0003g0125 |
4 | HG03209.hp1 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+197T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399901 | |||||||
| chr1:10399983 | C | T | 7 | a0001c0004t0001g0113 a0001c0004t0001g0114 a0001c0004t0001g0115 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+279C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10399983 | |||||||
| chr1:10400028 | T | C | 3 | a0001c0004t0003g0023 a0001c0004t0003g0121 a0001c0004t0013g0120 |
5 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+324T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 2/12 | chr1 | 10400028 | |||||||
| chr1:10400595 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.264+23C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10400595 | |||||||
| chr1:10400612 | G | A | 1 | a0001c0002t0007g0193 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.264+40G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10400612 | |||||||
| chr1:10400659 | A | AT | 122 | a0001c0001t0001g0014 a0001c0001t0003g0011 a0001c0001t0003g0014 others(119): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.264+98dupT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 10400659 | ||||||
| chr1:10400677 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.264+105C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10400677 | |||||||
| chr1:10400811 | G | C | 11 | a0001c0004t0001g0035 a0001c0004t0001g0066 a0001c0004t0001g0067 others(8): Show |
12 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+239G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10400811 | |||||||
| chr1:10401003 | G | A | 1 | a0001c0004t0013g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.264+431G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401003 | |||||||
| chr1:10401034 | G | A | 1 | a0001c0002t0001g0069 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.264+462G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401034 | |||||||
| chr1:10401050 | T | C | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.264+478T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401050 | |||||||
| chr1:10401074 | T | G | 4 | a0001c0001t0002g0195 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
5 | HG01167.hp1 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+502T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401074 | |||||||
| chr1:10401075 | C | T | 1 | a0001c0002t0001g0112 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.264+503C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401075 | |||||||
| chr1:10401120 | A | G | 137 | a0001c0001t0001g0014 a0001c0001t0002g0173 a0001c0001t0002g0195 others(134): Show |
218 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.264+548A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401120 | |||||||
| chr1:10401178 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.264+606G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401178 | |||||||
| chr1:10401396 | C | G | 1 | a0001c0004t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.264+824C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401396 | |||||||
| chr1:10401439 | C | T | 1 | a0001c0004t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.264+867C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401439 | |||||||
| chr1:10401573 | A | T | 1 | a0001c0002t0008g0111 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.264+1001A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401573 | |||||||
| chr1:10401617 | A | G | 1 | a0001c0004t0001g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.264+1045A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401617 | |||||||
| chr1:10401812 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.264+1240G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401812 | |||||||
| chr1:10401876 | G | A | 15 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0015 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.265-1195G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10401876 | |||||||
| chr1:10402022 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.265-1049T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402022 | |||||||
| chr1:10402027 | A | T | 5 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0109 others(2): Show |
5 | HG02602.hp1 HG02809.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-1044A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402027 | |||||||
| chr1:10402027 | AAATT | A | 16 | a0001c0001t0003g0197 a0002c0003t0001g0007 a0002c0003t0001g0009 others(13): Show |
29 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.265-1028_265-1025d others(6): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 10402027 | ||||||
| chr1:10402031 | T | A | 92 | a0001c0001t0001g0014 a0001c0001t0002g0001 a0001c0001t0002g0005 others(89): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.265-1040T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402031 | |||||||
| chr1:10402035 | T | A | 40 | a0001c0001t0001g0014 a0001c0001t0002g0128 a0001c0001t0002g0129 others(37): Show |
60 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.265-1036T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402035 | |||||||
| chr1:10402039 | T | A | 2 | a0001c0004t0003g0023 a0001c0004t0003g0121 |
4 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-1032T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402039 | |||||||
| chr1:10402195 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0004g0171 others(1): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-876C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402195 | |||||||
| chr1:10402340 | GA | G | 15 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0015 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.265-730delA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402340 | |||||||
| chr1:10402499 | C | T | 9 | a0001c0002t0001g0022 a0001c0002t0001g0039 a0001c0002t0001g0099 others(6): Show |
12 | HG00408.hp1 HG00558.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.265-572C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402499 | |||||||
| chr1:10402500 | G | A | 3 | a0001c0001t0002g0173 a0001c0001t0003g0192 a0001c0001t0004g0046 |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-571G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402500 | |||||||
| chr1:10402504 | T | G | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.265-567T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402504 | |||||||
| chr1:10402556 | T | C | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.265-515T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402556 | |||||||
| chr1:10402697 | G | A | 1 | a0001c0001t0012g0130 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.265-374G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402697 | |||||||
| chr1:10402813 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.265-258G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402813 | |||||||
| chr1:10402815 | G | A | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.265-256G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402815 | |||||||
| chr1:10402818 | T | C | 153 | a0001c0001t0001g0014 a0001c0001t0002g0024 a0001c0001t0002g0027 others(150): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.265-253T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402818 | |||||||
| chr1:10402833 | A | T | 1 | a0002c0003t0001g0063 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.265-238A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402833 | |||||||
| chr1:10402933 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.265-138G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402933 | |||||||
| chr1:10402982 | A | G | 1 | a0001c0002t0001g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265-89A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402982 | |||||||
| chr1:10402983 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.265-88T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 3/12 | chr1 | 10402983 | |||||||
| chr1:10403297 | C | T | 25 | a0001c0001t0001g0014 a0001c0001t0003g0011 a0001c0001t0003g0014 others(22): Show |
40 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.330+161C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403297 | |||||||
| chr1:10403410 | C | T | 16 | a0001c0004t0001g0110 a0002c0003t0001g0007 a0002c0003t0001g0009 others(13): Show |
29 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.330+274C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403410 | |||||||
| chr1:10403515 | T | C | 129 | a0001c0001t0001g0014 a0001c0001t0002g0173 a0001c0001t0003g0011 others(126): Show |
209 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.330+379T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403515 | |||||||
| chr1:10403531 | C | T | 15 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0015 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.330+395C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403531 | |||||||
| chr1:10403534 | T | G | 11 | a0001c0001t0002g0024 a0001c0001t0002g0040 a0001c0001t0002g0131 others(8): Show |
13 | HG00639.hp2 HG01256.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.330+398T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403534 | |||||||
| chr1:10403539 | C | G | 1 | a0001c0011t0002g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.330+403C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403539 | |||||||
| chr1:10403569 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.330+433C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403569 | |||||||
| chr1:10403590 | G | GA | 11 | a0001c0001t0002g0140 a0001c0001t0002g0173 a0001c0001t0003g0028 others(8): Show |
13 | HG00735.hp2 HG01192.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.330+474dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | G | GAA | 9 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0002g0195 others(6): Show |
12 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.330+473_330+474dup others(2): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | G | GAAAA | 14 | a0001c0004t0001g0110 a0002c0003t0001g0007 a0002c0003t0001g0009 others(11): Show |
27 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.330+471_330+474dup others(4): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | G | GAAAAA | 8 | a0001c0002t0001g0021 a0001c0002t0001g0097 a0001c0002t0001g0098 others(5): Show |
11 | HG00673.hp1 HG02615.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.330+470_330+474dup others(5): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | G | GAAAAAA | 49 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(46): Show |
90 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.330+469_330+474dup others(6): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | G | GAAAAAAA | 25 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 others(22): Show |
32 | HG00408.hp1 HG00558.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.330+468_330+474dup others(7): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403590 | GA | G | 6 | a0001c0001t0002g0045 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
7 | HG00323.hp1 HG01257.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.330+474delA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10403590 | ||||||
| chr1:10403753 | A | G | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331-408A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403753 | |||||||
| chr1:10403831 | C | A | 142 | a0001c0001t0001g0014 a0001c0001t0002g0027 a0001c0001t0002g0170 others(139): Show |
227 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.331-330C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403831 | |||||||
| chr1:10403904 | T | C | 1 | a0001c0002t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.331-257T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10403904 | |||||||
| chr1:10404093 | TAGCATAA others(11): Show |
T | 11 | a0001c0004t0001g0035 a0001c0004t0001g0066 a0001c0004t0001g0067 others(8): Show |
12 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.331-37_331-20delCA others(16): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 10404093 | ||||||
| chr1:10404118 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.331-43A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10404118 | |||||||
| chr1:10404120 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.331-41G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 4/12 | chr1 | 10404120 | |||||||
| chr1:10404522 | C | CT | 11 | a0001c0001t0002g0044 a0001c0001t0002g0164 a0001c0001t0002g0166 others(8): Show |
13 | HG01243.hp2 HG02027.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.449+256dupT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10404522 | ||||||
| chr1:10404522 | CT | C | 25 | a0001c0001t0001g0014 a0001c0001t0003g0011 a0001c0001t0003g0014 others(22): Show |
40 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.449+256delT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10404522 | ||||||
| chr1:10404877 | T | C | 1 | a0001c0004t0001g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.449+598T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10404877 | |||||||
| chr1:10404981 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.449+702C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10404981 | |||||||
| chr1:10405038 | TC | T | 3 | a0001c0004t0003g0023 a0001c0004t0003g0121 a0001c0004t0013g0120 |
5 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+761delC | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405038 | ||||||
| chr1:10405234 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0004g0171 others(1): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.449+955A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405234 | |||||||
| chr1:10405242 | G | A | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.449+963G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405242 | |||||||
| chr1:10405245 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0004g0161 |
2 | NA18967.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.449+966C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405245 | |||||||
| chr1:10405336 | A | G | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.449+1057A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405336 | |||||||
| chr1:10405392 | AAC | A | 15 | a0001c0004t0001g0066 a0002c0003t0001g0007 a0002c0003t0001g0009 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.449+1115_449+1116d others(4): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405392 | ||||||
| chr1:10405394 | C | A | 82 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(79): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.449+1115C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405394 | |||||||
| chr1:10405395 | A | AATACAC | 4 | a0001c0004t0001g0110 a0001c0004t0001g0122 a0001c0004t0001g0123 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.449+1117_449+1118i others(8): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405395 | ||||||
| chr1:10405395 | A | AATACACA others(3): Show |
2 | a0001c0002t0001g0077 a0001c0004t0003g0121 |
2 | HG01975.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.449+1117_449+1118i others(12): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405395 | ||||||
| chr1:10405395 | A | AATACACA others(5): Show |
1 | a0001c0004t0013g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.449+1117_449+1118i others(14): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405395 | ||||||
| chr1:10405395 | A | AATACACA others(7): Show |
2 | a0001c0004t0003g0023 a0001c0013t0001g0106 |
4 | HG02280.hp2 HG02896.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.449+1117_449+1118i others(16): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405395 | ||||||
| chr1:10405397 | A | C | 9 | a0001c0002t0001g0077 a0001c0004t0001g0110 a0001c0004t0001g0122 others(6): Show |
11 | HG01891.hp2 HG01975.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.449+1118A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405397 | |||||||
| chr1:10405397 | A | T | 73 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(70): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.449+1118A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405397 | |||||||
| chr1:10405399 | A | C | 82 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(79): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.449+1120A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405399 | |||||||
| chr1:10405399 | A | T | 15 | a0001c0004t0001g0066 a0002c0003t0001g0007 a0002c0003t0001g0009 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.449+1120A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405399 | |||||||
| chr1:10405401 | T | C | 97 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(94): Show |
160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.449+1122T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405401 | |||||||
| chr1:10405401 | T | TAC | 10 | a0001c0001t0002g0041 a0001c0001t0002g0167 a0001c0001t0003g0051 others(7): Show |
12 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.449+1146_449+1147d others(4): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(3): Show |
1 | a0001c0011t0002g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.449+1138_449+1147d others(12): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(5): Show |
11 | a0001c0001t0003g0011 a0001c0001t0003g0028 a0001c0001t0003g0031 others(8): Show |
19 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.449+1136_449+1147d others(14): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(7): Show |
3 | a0001c0001t0003g0030 a0001c0001t0003g0048 a0001c0001t0003g0187 |
6 | HG01074.hp2 HG02056.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.449+1134_449+1147d others(16): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(9): Show |
6 | a0001c0001t0001g0014 a0001c0001t0003g0014 a0001c0001t0003g0047 others(3): Show |
9 | HG01109.hp2 HG02055.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.449+1132_449+1147d others(18): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(11): Show |
3 | a0001c0001t0002g0173 a0001c0001t0003g0029 a0001c0014t0003g0029 |
4 | HG02257.hp2 HG02451.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.449+1130_449+1147d others(20): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405401 | T | TACACACA others(13): Show |
1 | a0001c0001t0003g0186 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.449+1128_449+1147d others(22): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405401 | ||||||
| chr1:10405425 | C | CACACACA others(7): Show |
5 | a0001c0001t0004g0046 a0001c0002t0001g0070 a0001c0002t0001g0074 others(2): Show |
6 | HG02040.hp2 HG02148.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.449+1147_449+1148i others(16): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405425 | ||||||
| chr1:10405425 | C | CACACACA others(5): Show |
19 | a0001c0002t0001g0016 a0001c0002t0001g0022 a0001c0002t0001g0038 others(16): Show |
25 | HG00408.hp1 HG00558.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.449+1147_449+1148i others(14): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405425 | ||||||
| chr1:10405425 | C | CACACACA others(3): Show |
25 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0017 others(22): Show |
48 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.449+1147_449+1148i others(12): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405425 | ||||||
| chr1:10405425 | C | CACACACA others(1): Show |
15 | a0001c0001t0003g0192 a0001c0002t0001g0002 a0001c0002t0001g0012 others(12): Show |
31 | HG00280.hp2 HG00408.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.449+1147_449+1148i others(10): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405425 | ||||||
| chr1:10405425 | C | CACACAT | 1 | a0001c0002t0001g0020 | 3 | HG01069.hp2 HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.449+1147_449+1148i others(8): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405425 | ||||||
| chr1:10405427 | T | C | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.449+1148T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405427 | |||||||
| chr1:10405581 | T | C | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.449+1302T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405581 | |||||||
| chr1:10405598 | G | A | 3 | a0001c0004t0003g0023 a0001c0004t0003g0121 a0001c0004t0013g0120 |
5 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.449+1319G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405598 | |||||||
| chr1:10405779 | T | C | 1 | a0001c0002t0001g0017 | 3 | HG00735.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.449+1500T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405779 | |||||||
| chr1:10405829 | CG | C | 25 | a0001c0001t0001g0014 a0001c0001t0003g0011 a0001c0001t0003g0014 others(22): Show |
40 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.449+1552delG | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10405829 | ||||||
| chr1:10405878 | G | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0076 |
2 | HG02040.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.449+1599G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405878 | |||||||
| chr1:10405983 | G | A | 101 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 others(98): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.449+1704G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405983 | |||||||
| chr1:10405989 | A | G | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.449+1710A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10405989 | |||||||
| chr1:10406054 | C | T | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.449+1775C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406054 | |||||||
| chr1:10406376 | C | G | 3 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0124 |
3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.450-1695C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406376 | |||||||
| chr1:10406376 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.450-1695C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406376 | |||||||
| chr1:10406388 | GA | G | 10 | a0001c0001t0003g0029 a0001c0001t0003g0181 a0001c0001t0003g0186 others(7): Show |
13 | HG01109.hp2 HG01243.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.450-1671delA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10406388 | ||||||
| chr1:10406514 | G | T | 1 | a0001c0006t0002g0025 | 3 | HG02922.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.450-1557G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406514 | |||||||
| chr1:10406556 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.450-1515C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406556 | |||||||
| chr1:10406766 | G | C | 1 | a0001c0001t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.450-1305G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406766 | |||||||
| chr1:10406872 | A | T | 1 | a0001c0002t0001g0094 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.450-1199A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406872 | |||||||
| chr1:10406964 | A | C | 1 | a0001c0004t0013g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450-1107A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10406964 | |||||||
| chr1:10407017 | G | A | 137 | a0001c0001t0001g0014 a0001c0001t0002g0173 a0001c0001t0002g0195 others(134): Show |
218 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.450-1054G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407017 | |||||||
| chr1:10407217 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.450-854G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407217 | |||||||
| chr1:10407399 | G | A | 3 | a0001c0001t0002g0128 a0001c0001t0002g0129 a0001c0001t0002g0142 |
3 | HG00741.hp1 HG01069.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.450-672G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407399 | |||||||
| chr1:10407522 | G | A | 2 | a0002c0005t0001g0054 a0002c0005t0001g0055 |
2 | NA19062.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.450-549G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407522 | |||||||
| chr1:10407580 | G | T | 1 | a0001c0001t0004g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.450-491G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407580 | |||||||
| chr1:10407743 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0168 a0001c0001t0003g0157 others(2): Show |
14 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-328C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407743 | |||||||
| chr1:10407744 | G | A | 1 | a0001c0013t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450-327G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407744 | |||||||
| chr1:10407861 | A | G | 1 | a0001c0013t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.450-210A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407861 | |||||||
| chr1:10407940 | C | A | 1 | a0001c0002t0001g0081 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.450-131C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | chr1 | 10407940 | |||||||
| chr1:10407948 | C | CA | 6 | a0001c0001t0002g0006 a0001c0001t0002g0042 a0001c0001t0002g0143 others(3): Show |
14 | HG00639.hp1 HG01099.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.450-108dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10407948 | ||||||
| chr1:10407980 | GGTTGGTG others(11): Show |
G | 4 | a0001c0002t0001g0074 a0001c0004t0003g0023 a0001c0004t0003g0121 others(1): Show |
6 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.450-71_450-54delTT others(16): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 10407980 | ||||||
| chr1:10408234 | G | T | 1 | a0001c0001t0002g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.519+94G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408234 | |||||||
| chr1:10408253 | C | T | 1 | a0001c0001t0003g0048 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.519+113C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408253 | |||||||
| chr1:10408448 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.519+308A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408448 | |||||||
| chr1:10408502 | A | G | 3 | a0001c0004t0003g0023 a0001c0004t0003g0121 a0001c0004t0013g0120 |
5 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+362A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408502 | |||||||
| chr1:10408505 | G | A | 2 | a0001c0004t0001g0122 a0001c0004t0001g0123 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.519+365G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408505 | |||||||
| chr1:10408521 | A | G | 1 | a0001c0001t0002g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.519+381A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408521 | |||||||
| chr1:10408755 | C | T | 2 | a0001c0004t0003g0023 a0001c0004t0003g0121 |
4 | HG02280.hp2 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+615C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408755 | |||||||
| chr1:10408889 | G | A | 81 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(78): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.519+749G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408889 | |||||||
| chr1:10408904 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.519+764C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408904 | |||||||
| chr1:10408913 | G | C | 4 | a0001c0001t0003g0029 a0001c0001t0003g0181 a0001c0001t0003g0186 others(1): Show |
5 | HG01109.hp2 HG01257.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+773G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10408913 | |||||||
| chr1:10409007 | C | A | 2 | a0001c0001t0003g0197 a0001c0001t0003g0198 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.519+867C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409007 | |||||||
| chr1:10409048 | G | A | 2 | a0001c0001t0005g0032 a0001c0001t0009g0032 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.519+908G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409048 | |||||||
| chr1:10409381 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.519+1241C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409381 | |||||||
| chr1:10409524 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.519+1384C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409524 | |||||||
| chr1:10409584 | A | G | 99 | a0001c0001t0003g0051 a0001c0002t0001g0002 a0001c0002t0001g0004 others(96): Show |
162 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.519+1444A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409584 | |||||||
| chr1:10409604 | A | G | 4 | a0001c0001t0002g0195 a0001c0001t0003g0049 a0001c0001t0003g0050 others(1): Show |
5 | HG01167.hp1 HG02145.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+1464A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409604 | |||||||
| chr1:10409612 | A | C | 1 | a0001c0002t0001g0075 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.519+1472A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409612 | |||||||
| chr1:10409649 | C | CT | 18 | a0001c0001t0001g0014 a0001c0001t0002g0008 a0001c0001t0002g0129 others(15): Show |
27 | HG00741.hp1 HG01167.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.519+1535dupT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | C | CTTTT | 15 | a0001c0002t0001g0078 a0001c0002t0001g0082 a0001c0002t0001g0094 others(12): Show |
23 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.519+1532_519+1535d others(6): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | C | CTTTTT | 43 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(40): Show |
87 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.519+1531_519+1535d others(7): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | C | CTTTTTT | 24 | a0001c0001t0003g0051 a0001c0002t0001g0010 a0001c0002t0001g0037 others(21): Show |
31 | HG00408.hp2 HG00558.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+1530_519+1535d others(8): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | C | CTTTTTTT | 6 | a0001c0002t0001g0022 a0001c0002t0001g0088 a0001c0002t0001g0091 others(3): Show |
8 | HG00408.hp1 HG02630.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+1529_519+1535d others(9): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | C | CTTTTTTT others(1): Show |
6 | a0001c0004t0001g0113 a0001c0004t0001g0115 a0001c0004t0001g0117 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+1528_519+1535d others(10): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409649 | CT | C | 20 | a0001c0001t0002g0027 a0001c0001t0002g0143 a0001c0001t0002g0170 others(17): Show |
32 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.519+1535delT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10409649 | ||||||
| chr1:10409650 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.519+1510T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409650 | |||||||
| chr1:10409709 | G | A | 1 | a0001c0001t0002g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.519+1569G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409709 | |||||||
| chr1:10409741 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519+1601C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409741 | |||||||
| chr1:10409802 | T | C | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 |
4 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-1616T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409802 | |||||||
| chr1:10409931 | T | C | 3 | a0001c0001t0002g0026 a0001c0001t0010g0026 a0001c0001t0011g0026 |
3 | NA18953.hp1 NA18974.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.520-1487T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409931 | |||||||
| chr1:10409994 | C | T | 1 | a0001c0011t0002g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.520-1424C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10409994 | |||||||
| chr1:10410103 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520-1315A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10410103 | |||||||
| chr1:10410118 | C | T | 15 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0015 others(12): Show |
28 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.520-1300C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10410118 | |||||||
| chr1:10410498 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.520-920C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10410498 | |||||||
| chr1:10410789 | G | T | 102 | a0001c0001t0003g0051 a0001c0001t0005g0032 a0001c0001t0005g0033 others(99): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.520-629G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10410789 | |||||||
| chr1:10410844 | T | TTATAAA | 4 | a0001c0001t0003g0183 a0001c0001t0003g0188 a0001c0002t0001g0109 others(1): Show |
4 | HG01891.hp2 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-550_520-545dup others(6): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10410844 | ||||||
| chr1:10410844 | T | TTATAAAT others(5): Show |
1 | a0001c0001t0003g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.520-556_520-545dup others(12): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 10410844 | ||||||
| chr1:10410923 | T | G | 17 | a0001c0004t0001g0110 a0001c0007t0001g0064 a0002c0003t0001g0007 others(14): Show |
30 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-495T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10410923 | |||||||
| chr1:10411025 | C | T | 1 | a0001c0006t0002g0025 | 3 | HG02922.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.520-393C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10411025 | |||||||
| chr1:10411138 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.520-280A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10411138 | |||||||
| chr1:10411336 | T | C | 4 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-82T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10411336 | |||||||
| chr1:10411361 | T | G | 1 | a0001c0001t0002g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.520-57T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10411361 | |||||||
| chr1:10411374 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.520-44C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 6/12 | chr1 | 10411374 | |||||||
| chr1:10411563 | G | A | 1 | a0001c0004t0003g0023 | 3 | HG02280.hp2 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.654+11G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411563 | |||||||
| chr1:10411703 | C | T | 12 | a0001c0001t0002g0003 a0001c0001t0002g0140 a0001c0001t0002g0151 others(9): Show |
23 | HG01928.hp2 HG01993.hp2 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.654+151C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411703 | |||||||
| chr1:10411732 | A | T | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.654+180A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411732 | |||||||
| chr1:10411778 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0004g0171 others(1): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+226C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411778 | |||||||
| chr1:10411909 | A | T | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.654+357A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411909 | |||||||
| chr1:10411969 | C | A | 131 | a0001c0001t0001g0014 a0001c0001t0002g0173 a0001c0001t0003g0011 others(128): Show |
211 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.654+417C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10411969 | |||||||
| chr1:10412028 | ACCT | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0004g0171 others(1): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+483_654+485del others(3): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 10412028 | ||||||
| chr1:10412133 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0004g0046 |
3 | HG02451.hp1 HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.654+581C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412133 | |||||||
| chr1:10412183 | T | C | 4 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0095 others(1): Show |
8 | NA18943.hp1 NA18948.hp2 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+631T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412183 | |||||||
| chr1:10412213 | A | T | 1 | a0001c0001t0002g0163 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.654+661A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412213 | |||||||
| chr1:10412701 | C | A | 1 | a0001c0004t0001g0110 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.655-361C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412701 | |||||||
| chr1:10412734 | C | T | 1 | a0001c0008t0002g0165 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.655-328C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412734 | |||||||
| chr1:10412791 | C | G | 141 | a0001c0001t0001g0014 a0001c0001t0002g0027 a0001c0001t0002g0170 others(138): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.655-271C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | chr1 | 10412791 | |||||||
| chr1:10412812 | GTGAGGAG others(10): Show |
G | 3 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 |
4 | HG01256.hp1 HG01258.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.655-242_655-226del others(17): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | 10412812 | ||||||
| chr1:10413654 | C | T | 1 | a0001c0004t0001g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.844+403C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10413654 | |||||||
| chr1:10413775 | C | T | 5 | a0001c0002t0001g0016 a0001c0002t0001g0071 a0001c0002t0001g0075 others(2): Show |
7 | HG01433.hp2 HG01496.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.844+524C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10413775 | |||||||
| chr1:10413891 | C | CT | 6 | a0001c0001t0002g0195 a0001c0001t0003g0049 a0001c0001t0003g0050 others(3): Show |
7 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.844+640_844+641ins others(1): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10413891 | |||||||
| chr1:10413904 | C | CA | 27 | a0001c0001t0001g0014 a0001c0001t0002g0159 a0001c0001t0003g0011 others(24): Show |
42 | HG00323.hp1 HG00733.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.844+668dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 10413904 | ||||||
| chr1:10413904 | CA | C | 25 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0195 others(22): Show |
39 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.844+668delA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 10413904 | ||||||
| chr1:10414295 | A | T | 11 | a0001c0004t0001g0035 a0001c0004t0001g0066 a0001c0004t0001g0067 others(8): Show |
12 | HG01243.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.844+1044A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414295 | |||||||
| chr1:10414373 | A | T | 101 | a0001c0001t0005g0032 a0001c0001t0005g0033 a0001c0001t0009g0032 others(98): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.844+1122A>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414373 | |||||||
| chr1:10414400 | T | A | 142 | a0001c0001t0001g0014 a0001c0001t0002g0027 a0001c0001t0002g0170 others(139): Show |
227 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.844+1149T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414400 | |||||||
| chr1:10414421 | C | A | 3 | a0001c0004t0001g0114 a0001c0004t0001g0115 a0001c0004t0001g0119 |
3 | HG01243.hp2 HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.844+1170C>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414421 | |||||||
| chr1:10414500 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0004g0013 |
4 | NA18962.hp2 NA18979.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+1249G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414500 | |||||||
| chr1:10414560 | G | A | 1 | a0001c0013t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.844+1309G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414560 | |||||||
| chr1:10414629 | G | A | 5 | a0002c0005t0001g0054 a0002c0005t0001g0055 a0002c0005t0001g0056 others(2): Show |
5 | NA18941.hp1 NA19058.hp2 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.844+1378G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414629 | |||||||
| chr1:10414732 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.844+1481C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414732 | |||||||
| chr1:10414796 | A | G | 1 | a0001c0011t0002g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.844+1545A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414796 | |||||||
| chr1:10414920 | A | G | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.844+1669A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414920 | |||||||
| chr1:10414954 | A | G | 153 | a0001c0001t0001g0014 a0001c0001t0002g0024 a0001c0001t0002g0027 others(150): Show |
240 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.844+1703A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10414954 | |||||||
| chr1:10415063 | G | C | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.844+1812G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415063 | |||||||
| chr1:10415089 | T | TA | 95 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(92): Show |
156 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.844+1851dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 10415089 | ||||||
| chr1:10415122 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.845-1865A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415122 | |||||||
| chr1:10415163 | C | G | 1 | a0001c0002t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.845-1824C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415163 | |||||||
| chr1:10415193 | T | A | 1 | a0001c0002t0001g0078 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.845-1794T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415193 | |||||||
| chr1:10415291 | A | AAGGAAGT others(11): Show |
1 | a0001c0001t0002g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.845-1693_845-1676d others(20): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 10415291 | ||||||
| chr1:10415480 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.845-1507G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415480 | |||||||
| chr1:10415870 | A | C | 3 | a0001c0002t0001g0019 a0001c0002t0001g0087 a0001c0002t0001g0109 |
5 | HG01884.hp2 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-1117A>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10415870 | |||||||
| chr1:10416356 | T | G | 2 | a0001c0004t0001g0035 a0001c0004t0001g0066 |
3 | HG02615.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.845-631T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416356 | |||||||
| chr1:10416527 | G | T | 1 | a0001c0001t0003g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.845-460G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416527 | |||||||
| chr1:10416528 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.845-459C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416528 | |||||||
| chr1:10416555 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.845-432A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416555 | |||||||
| chr1:10416632 | T | C | 1 | a0001c0001t0003g0175 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.845-355T>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416632 | |||||||
| chr1:10416714 | G | A | 1 | a0001c0004t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.845-273G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416714 | |||||||
| chr1:10416883 | G | A | 2 | a0001c0002t0001g0086 a0001c0002t0014g0084 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.845-104G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 8/12 | chr1 | 10416883 | |||||||
| chr1:10417177 | G | A | 1 | a0001c0001t0004g0146 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.975+60G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 9/12 | chr1 | 10417177 | |||||||
| chr1:10417534 | C | T | 1 | a0001c0001t0002g0043 | 2 | NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1109+25C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10417534 | |||||||
| chr1:10417569 | G | A | 2 | a0001c0001t0003g0192 a0001c0001t0003g0198 |
2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1109+60G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10417569 | |||||||
| chr1:10417768 | G | C | 2 | a0002c0003t0001g0034 a0002c0003t0003g0053 |
3 | HG00423.hp1 NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1109+259G>C | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10417768 | |||||||
| chr1:10417855 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0004g0171 others(1): Show |
6 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109+346G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10417855 | |||||||
| chr1:10417922 | G | T | 1 | a0001c0006t0002g0025 | 3 | HG02922.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1109+413G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10417922 | |||||||
| chr1:10418060 | A | G | 3 | a0001c0001t0002g0042 a0001c0001t0002g0147 a0001c0002t0001g0081 |
4 | NA18947.hp2 NA18961.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1109+551A>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418060 | |||||||
| chr1:10418082 | CTT | C | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1109+574_1109+575d others(4): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418082 | |||||||
| chr1:10418106 | C | T | 3 | a0001c0002t0001g0019 a0001c0002t0001g0087 a0001c0002t0001g0109 |
5 | HG01884.hp2 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109+597C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418106 | |||||||
| chr1:10418160 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1109+651C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418160 | |||||||
| chr1:10418292 | C | G | 1 | a0001c0001t0012g0130 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1110-534C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418292 | |||||||
| chr1:10418529 | C | T | 104 | a0001c0001t0002g0024 a0001c0001t0002g0132 a0001c0001t0002g0137 others(101): Show |
168 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1110-297C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418529 | |||||||
| chr1:10418543 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1110-283G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418543 | |||||||
| chr1:10418667 | G | T | 1 | a0001c0001t0003g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110-159G>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418667 | |||||||
| chr1:10418669 | C | G | 1 | a0001c0001t0003g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1110-157C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418669 | |||||||
| chr1:10418670 | G | A | 98 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(95): Show |
161 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1110-156G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418670 | |||||||
| chr1:10418689 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1110-137C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418689 | |||||||
| chr1:10418760 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1110-66C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | chr1 | 10418760 | |||||||
| chr1:10418773 | C | CA | 93 | a0001c0001t0002g0170 a0001c0001t0003g0125 a0001c0001t0003g0150 others(90): Show |
152 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1110-36dupA | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 10418773 | ||||||
| chr1:10418773 | C | CAA | 8 | a0001c0002t0001g0019 a0001c0002t0001g0087 a0001c0002t0001g0095 others(5): Show |
12 | HG01884.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1110-37_1110-36dup others(2): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 10418773 | ||||||
| chr1:10418998 | G | GT | 6 | a0001c0002t0001g0018 a0001c0002t0001g0092 a0001c0002t0001g0101 others(3): Show |
8 | HG00558.hp1 HG03491.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209+85dupT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 10418998 | ||||||
| chr1:10419094 | C | T | 1 | a0001c0004t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1209+169C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | chr1 | 10419094 | |||||||
| chr1:10419174 | A | AT | 94 | a0001c0001t0003g0150 a0001c0001t0003g0157 a0001c0001t0003g0181 others(91): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1210-227dupT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 10419174 | ||||||
| chr1:10419174 | A | ATT | 7 | a0001c0002t0001g0080 a0001c0002t0001g0085 a0001c0004t0001g0114 others(4): Show |
7 | HG01123.hp2 HG01981.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1210-228_1210-227d others(4): Show |
PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 10419174 | ||||||
| chr1:10419174 | AT | A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0170 a0001c0001t0003g0182 others(2): Show |
7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-227delT | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 10419174 | ||||||
| chr1:10419296 | C | T | 11 | a0001c0007t0001g0064 a0002c0003t0001g0007 a0002c0003t0001g0009 others(8): Show |
24 | HG00423.hp1 HG00741.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1210-121C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | chr1 | 10419296 | |||||||
| chr1:10419391 | T | G | 1 | a0001c0001t0002g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1210-26T>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 11/12 | chr1 | 10419391 | |||||||
| chr1:10419578 | C | G | 132 | a0001c0001t0001g0014 a0001c0001t0002g0173 a0001c0001t0002g0195 others(129): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1332+39C>G | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 12/12 | chr1 | 10419578 | |||||||
| chr1:10419607 | C | T | 1 | a0001c0010t0016g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1333-23C>T | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 12/12 | chr1 | 10419607 | |||||||
| chr1:10419615 | T | A | 1 | a0001c0002t0001g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1333-15T>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 12/12 | chr1 | 10419615 | |||||||
| chr1:10419621 | G | A | 67 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0010 others(64): Show |
114 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.1333-9G>A | PGD | ENSG00000142657.21 | transcript | ENST00000270776.13 | protein_coding | 12/12 | chr1 | 10419621 |