Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3248 |
| ensemblid | ENSG00000164120.14 |
| hgncid | 5154 |
| symbol | HPGD |
| name | 15-hydroxyprostaglandin dehydrogenase |
| refseq_nuc | NM_000860.6 |
| refseq_prot | NP_000851.2 |
| ensembl_nuc | ENST00000296522.11 |
| ensembl_prot | ENSP00000296522.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 174490175 |
| end | 174522488 |
| strand | - |
| ver | v1.2 |
| region | chr4:174490175-174522488 |
| region5000 | chr4:174485175-174527488 |
| regionname0 | HPGD_chr4_174490175_174522488 |
| regionname5000 | HPGD_chr4_174485175_174527488 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 266 | 408 | 89 | 67 | 186 | 16 | 48 | 146 | HPGD_chr4_174485175_174527488 | HPGD | MHVNG others(261): Show |
chr4 | 174485175 | 174527488 |
| a0002 | 0/0 | 266 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | MHVNG others(261): Show |
chr4 | 174485175 | 174527488 |
| a0003 | 0/0 | 266 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HPGD_chr4_174485175_174527488 | HPGD | MHVNG others(261): Show |
chr4 | 174485175 | 174527488 |
| a0004 | 0/0 | 266 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | MHVNG others(261): Show |
chr4 | 174485175 | 174527488 |
| a0005 | 0/0 | 261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | MHVNG others(256): Show |
chr4 | 174485175 | 174527488 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 798 | 258 | 53 | 46 | 109 | 11 | 37 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0001c0002 | 0/0 | 798 | 139 | 25 | 21 | 77 | 5 | 11 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0001c0003 | 0/0 | 798 | 8 | 8 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0001c0005 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0001c0008 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0002c0004 | 0/0 | 798 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0003c0006 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0003c0007 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0004c0010 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 | ||
| a0005c0009 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | ATGCA others(793): Show |
chr4 | 174485175 | 174527488 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2619 | 93 | 10 | 20 | 41 | 5 | 16 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0002 | 0/0 | 2619 | 74 | 8 | 9 | 42 | 4 | 11 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0003 | 1/0 | 2619 | 50 | 8 | 10 | 21 | 1 | 9 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0004 | 0/0 | 2619 | 14 | 12 | 1 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0005 | 0/0 | 2619 | 8 | 7 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0006 | 0/0 | 2615 | 4 | 3 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2610): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0007 | 0/0 | 2619 | 4 | 3 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0008 | 0/0 | 2619 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0010 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0011 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0012 | 0/0 | 2607 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2602): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0013 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0014 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0016 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0017 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0018 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0001t0020 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0001 | 0/0 | 2619 | 47 | 5 | 9 | 27 | 3 | 3 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0002 | 0/0 | 2619 | 48 | 2 | 5 | 36 | 0 | 5 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0003 | 0/0 | 2619 | 27 | 3 | 7 | 13 | 2 | 2 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0004 | 0/0 | 2619 | 5 | 5 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0005 | 0/0 | 2619 | 9 | 9 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0006 | 0/0 | 2615 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2610): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0015 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0002t0019 | 0/0 | 2619 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0003t0001 | 0/0 | 2619 | 7 | 7 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0003t0009 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0005t0001 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0005t0009 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0001c0008t0005 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0002c0004t0001 | 0/0 | 2619 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0003c0006t0002 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0003c0007t0002 | 0/0 | 2619 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0004c0010t0002 | 0/0 | 2619 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| a0005c0009t0001 | 0/0 | 2619 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | GAGCT others(2614): Show |
chr4 | 174485175 | 174527488 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0012 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0006g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0008g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0010g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0011g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0013g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0014g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0017g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0018g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0001t0020g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0006 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0001 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0015g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0002t0019g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0003t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0005t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0001c0008t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0002c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0002c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0003c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0003c0007t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0004c0010t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| a0005c0009t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0199 | EUR | GBR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0158 | EUR | FIN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0094 | EUR | FIN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0071 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00609 | hp2 | a0001 | c0001 | t0010 | g0269 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0117 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0039 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0095 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0039 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0294 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01243 | hp2 | a0001 | c0001 | t0020 | g0310 | AMR | PUR | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01257 | hp2 | a0002 | c0004 | t0001 | g0096 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0104 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0055 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0072 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0101 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0196 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | IBS | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01884 | hp2 | a0001 | c0005 | t0009 | g0138 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01943 | hp1 | a0004 | c0010 | t0002 | g0275 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0143 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0134 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0330 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | CDX | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | CDX | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0091 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0144 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0129 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0312 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | KHV | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0127 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0263 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0132 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0131 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02717 | hp2 | a0001 | c0002 | t0005 | g0108 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0137 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0125 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0124 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0321 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0186 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0126 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0324 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0323 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0157 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0303 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | ESN | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | GWD | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0142 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03710 | hp2 | a0001 | c0001 | t0018 | g0232 | SAS | PJL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0103 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0077 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03942 | hp2 | a0001 | c0002 | t0019 | g0099 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0118 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0175 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0169 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0136 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18942 | hp1 | a0001 | c0002 | t0015 | g0074 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0113 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0114 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18978 | hp2 | a0003 | c0006 | t0002 | g0050 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18985 | hp2 | a0001 | c0001 | t0013 | g0325 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18994 | hp2 | a0001 | c0001 | t0014 | g0295 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18997 | hp1 | a0001 | c0001 | t0012 | g0205 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19004 | hp1 | a0003 | c0007 | t0002 | g0236 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0093 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | YRI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ASW | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20129 | hp2 | a0001 | c0008 | t0005 | g0322 | AFR | ASW | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0154 | EUR | TSI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0109 | EUR | TSI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | TSI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0098 | EUR | TSI | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | GIH | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0170 | AMR | CLM | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02486 | hp1 | a0005 | c0009 | t0001 | g0123 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0139 | AFR | ACB | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03471 | hp1 | a0001 | c0003 | t0009 | g0301 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG03471 | hp2 | a0001 | c0002 | t0005 | g0092 | AFR | MSL | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | USA | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | USA | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | USA | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA20300 | hp2 | a0001 | c0002 | t0005 | g0090 | AFR | USA | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0135 | AFR | LWK | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0284 | REF | REF | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0012 | REF | REF | HPGD_chr4_174485175_174527488 | HPGD | chr4 | 174485175 | 174527488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174491973 | G | A | 1 | a0005 | 1 | HG02486.hp1 | stop_gained | HIGH | c.784C>T | p.Gln262* | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 821/2619 | 784/801 | 262/266 | chr4 | 174491973 | |||
| chr4:174493179 | C | T | 1 | a0002 | 2 | HG01169.hp1 HG01257.hp2 |
missense_variant | MODERATE | c.634G>A | p.Asp212Asn | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/7 | 671/2619 | 634/801 | 212/266 | chr4 | 174493179 | |||
| chr4:174495576 | C | A | 1 | a0004 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.470G>T | p.Gly157Val | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/7 | 507/2619 | 470/801 | 157/266 | chr4 | 174495576 | |||
| chr4:174495613 | C | T | 1 | a0003 | 2 | NA18978.hp2 NA19004.hp1 |
missense_variant | MODERATE | c.433G>A | p.Val145Ile | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/7 | 470/2619 | 433/801 | 145/266 | chr4 | 174495613 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174493291 | A | G | 1 | a0001c0008 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.522T>C | p.Ser174Ser | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/7 | 559/2619 | 522/801 | 174/266 | chr4 | 174493291 | |||
| chr4:174495557 | G | A | 3 | a0001c0003 a0001c0005 a0005c0009 |
11 | HG01884.hp2 HG02486.hp1 HG02622.hp2 others(8): Show |
synonymous_variant | LOW | c.489C>T | p.Arg163Arg | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/7 | 526/2619 | 489/801 | 163/266 | chr4 | 174495557 | |||
| chr4:174522005 | C | T | 4 | a0001c0002 a0001c0005 a0002c0004 others(1): Show |
144 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
synonymous_variant | LOW | c.156G>A | p.Gln52Gln | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/7 | 193/2619 | 156/801 | 52/266 | chr4 | 174522005 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174490214 | A | G | 1 | a0001c0001t0013 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1742T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1742 | chr4 | 174490214 | ||||||
| chr4:174490230 | G | A | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(27): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*1726C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1726 | chr4 | 174490230 | ||||||
| chr4:174490231 | C | T | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(27): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*1725G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1725 | chr4 | 174490231 | ||||||
| chr4:174490259 | C | T | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1697 | chr4 | 174490259 | ||||||
| chr4:174490313 | T | C | 1 | a0001c0001t0008 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1643A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1643 | chr4 | 174490313 | ||||||
| chr4:174490377 | T | G | 1 | a0001c0001t0014 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1579A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1579 | chr4 | 174490377 | ||||||
| chr4:174490417 | T | A | 1 | a0001c0002t0015 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1539A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1539 | chr4 | 174490417 | ||||||
| chr4:174490442 | T | C | 1 | a0001c0001t0011 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1514A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1514 | chr4 | 174490442 | ||||||
| chr4:174490802 | A | G | 10 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(7): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1154T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1154 | chr4 | 174490802 | ||||||
| chr4:174490890 | C | T | 1 | a0001c0002t0001 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 1066 | chr4 | 174490890 | ||||||
| chr4:174491028 | TGGTTTTA others(5): Show |
T | 1 | a0001c0001t0012 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916_*927delGGAAAT others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 916 | chr4 | 174491028 | ||||||
| chr4:174491080 | T | C | 2 | a0001c0003t0009 a0001c0005t0009 |
2 | HG01884.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*876A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 876 | chr4 | 174491080 | ||||||
| chr4:174491308 | T | A | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 648 | chr4 | 174491308 | ||||||
| chr4:174491326 | C | T | 13 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0010 others(10): Show |
158 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*630G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 630 | chr4 | 174491326 | ||||||
| chr4:174491346 | GTCAA | G | 2 | a0001c0001t0006 a0001c0002t0006 |
5 | HG01109.hp1 HG02145.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*606_*609delTTGA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 606 | chr4 | 174491346 | ||||||
| chr4:174491538 | C | A | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0002t0004 others(2): Show |
37 | HG00639.hp1 HG01123.hp2 HG01884.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*418G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 418 | chr4 | 174491538 | ||||||
| chr4:174491824 | C | T | 3 | a0001c0001t0005 a0001c0002t0005 a0001c0008t0005 |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*132G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 132 | chr4 | 174491824 | ||||||
| chr4:174491825 | G | A | 1 | a0001c0001t0018 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 131 | chr4 | 174491825 | ||||||
| chr4:174491869 | T | C | 1 | a0001c0002t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 87 | chr4 | 174491869 | ||||||
| chr4:174491915 | T | C | 1 | a0001c0001t0020 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 7/7 | 41 | chr4 | 174491915 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:174492110 | A | G | 3 | a0001c0001t0002g0179 a0001c0001t0002g0191 a0001c0001t0002g0221 |
3 | HG01358.hp1 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.663-16T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492110 | |||||||
| chr4:174492124 | C | T | 5 | a0001c0001t0003g0008 a0001c0001t0003g0254 a0001c0001t0003g0255 others(2): Show |
8 | HG02135.hp2 NA18953.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.663-30G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492124 | |||||||
| chr4:174492125 | G | A | 1 | a0001c0001t0007g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-31C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492125 | |||||||
| chr4:174492145 | C | T | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.663-51G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492145 | |||||||
| chr4:174492166 | C | G | 1 | a0001c0001t0007g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-72G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492166 | |||||||
| chr4:174492187 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.663-93T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492187 | |||||||
| chr4:174492380 | T | C | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.663-286A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492380 | |||||||
| chr4:174492403 | A | T | 2 | a0001c0001t0006g0017 a0001c0002t0006g0093 |
4 | HG01109.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-309T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492403 | |||||||
| chr4:174492468 | A | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0203 |
2 | HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.663-374T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492468 | |||||||
| chr4:174492493 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
334 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.663-399T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492493 | |||||||
| chr4:174492500 | G | T | 2 | a0001c0001t0002g0256 a0001c0001t0002g0281 |
2 | HG02074.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.663-406C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492500 | |||||||
| chr4:174492614 | T | C | 1 | a0001c0001t0004g0330 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.663-520A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492614 | |||||||
| chr4:174492711 | A | G | 3 | a0001c0003t0001g0261 a0001c0003t0001g0264 a0005c0009t0001g0123 |
3 | HG02486.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.662+440T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492711 | |||||||
| chr4:174492777 | T | G | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.662+374A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174492777 | |||||||
| chr4:174493051 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
158 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.662+100G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174493051 | |||||||
| chr4:174493083 | T | C | 97 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.662+68A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174493083 | |||||||
| chr4:174493095 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
334 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(331): Show |
intron_variant | MODIFIER | c.662+56T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174493095 | |||||||
| chr4:174493127 | G | C | 97 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.662+24C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 6/6 | chr4 | 174493127 | |||||||
| chr4:174493505 | A | G | 98 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(95): Show |
133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.499-191T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174493505 | |||||||
| chr4:174493527 | T | A | 103 | a0001c0001t0001g0033 a0001c0001t0001g0172 a0001c0001t0001g0244 others(100): Show |
139 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.499-213A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174493527 | |||||||
| chr4:174493879 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.499-565C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174493879 | |||||||
| chr4:174493931 | G | A | 1 | a0001c0001t0011g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499-617C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174493931 | |||||||
| chr4:174494024 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.499-710A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494024 | |||||||
| chr4:174494219 | T | C | 2 | a0001c0001t0004g0028 a0001c0001t0004g0156 |
3 | HG01884.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.499-905A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494219 | |||||||
| chr4:174494291 | G | A | 97 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.499-977C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494291 | |||||||
| chr4:174494317 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.499-1003G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494317 | |||||||
| chr4:174494491 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.498+1057C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494491 | |||||||
| chr4:174494840 | G | A | 97 | a0001c0001t0001g0151 a0001c0001t0002g0007 a0001c0001t0002g0014 others(94): Show |
132 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.498+708C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174494840 | |||||||
| chr4:174495152 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.498+396G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174495152 | |||||||
| chr4:174495180 | C | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
304 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.498+368G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174495180 | |||||||
| chr4:174495329 | A | T | 1 | a0001c0001t0002g0328 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.498+219T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174495329 | |||||||
| chr4:174495368 | A | G | 2 | a0001c0001t0001g0299 a0001c0002t0001g0080 |
2 | HG02155.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.498+180T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174495368 | |||||||
| chr4:174495446 | C | A | 1 | a0001c0001t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.498+102G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 5/6 | chr4 | 174495446 | |||||||
| chr4:174495644 | C | T | 4 | a0001c0001t0004g0027 a0001c0001t0004g0195 a0001c0002t0004g0124 others(1): Show |
5 | HG00639.hp1 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.422-20G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174495644 | |||||||
| chr4:174495815 | G | A | 101 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(98): Show |
138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.422-191C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174495815 | |||||||
| chr4:174495819 | C | T | 1 | a0001c0001t0016g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.422-195G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174495819 | |||||||
| chr4:174495956 | A | G | 1 | a0001c0003t0001g0169 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.422-332T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174495956 | |||||||
| chr4:174496070 | G | C | 18 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(15): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.422-446C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496070 | |||||||
| chr4:174496106 | C | T | 1 | a0001c0002t0001g0145 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.422-482G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496106 | |||||||
| chr4:174496132 | G | A | 1 | a0001c0002t0005g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.422-508C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496132 | |||||||
| chr4:174496378 | G | GTAT | 101 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(98): Show |
138 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.422-757_422-755dup others(3): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496378 | |||||||
| chr4:174496496 | G | C | 99 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(96): Show |
136 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.422-872C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496496 | |||||||
| chr4:174496512 | T | A | 93 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(90): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-888A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496512 | |||||||
| chr4:174496569 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.422-945C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496569 | |||||||
| chr4:174496829 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.422-1205A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496829 | |||||||
| chr4:174496949 | G | A | 6 | a0001c0003t0001g0164 a0001c0003t0001g0167 a0001c0003t0001g0169 others(3): Show |
6 | HG02622.hp2 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.422-1325C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496949 | |||||||
| chr4:174496976 | G | A | 2 | a0001c0001t0004g0027 a0001c0001t0004g0195 |
3 | HG00639.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.422-1352C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174496976 | |||||||
| chr4:174497077 | T | C | 18 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(15): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.422-1453A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497077 | |||||||
| chr4:174497172 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0002t0001g0128 |
4 | HG01891.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-1548C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497172 | |||||||
| chr4:174497345 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.422-1721C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497345 | |||||||
| chr4:174497532 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.422-1908A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497532 | |||||||
| chr4:174497564 | C | T | 1 | a0001c0002t0004g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422-1940G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497564 | |||||||
| chr4:174497568 | C | CTTTCTT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0180 a0001c0001t0001g0314 others(3): Show |
7 | HG01433.hp2 HG01516.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(8): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT | 51 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(9): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(1): Show |
22 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0037 others(19): Show |
30 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(10): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(2): Show |
16 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0209 others(13): Show |
22 | HG00642.hp1 HG00741.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(11): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(3): Show |
9 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0283 others(6): Show |
9 | HG01069.hp2 HG01071.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(12): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(4): Show |
4 | a0001c0001t0001g0223 a0001c0001t0001g0246 a0001c0001t0001g0319 others(1): Show |
4 | HG01258.hp1 HG03669.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-1945_422-1944i others(13): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(5): Show |
1 | a0001c0001t0001g0292 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.422-1945_422-1944i others(14): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTCTTT others(8): Show |
1 | a0001c0002t0001g0097 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.422-1945_422-1944i others(17): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTCTT others(5): Show |
2 | a0001c0001t0004g0171 a0001c0001t0004g0195 |
2 | HG00639.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.422-1945_422-1944i others(14): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTCTT others(6): Show |
2 | a0001c0001t0004g0027 a0001c0002t0004g0125 |
3 | HG02257.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.422-1945_422-1944i others(15): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTCTT others(7): Show |
3 | a0001c0001t0004g0219 a0001c0001t0004g0222 a0001c0002t0004g0124 |
3 | HG02897.hp2 HG03579.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.422-1945_422-1944i others(16): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTCTT others(8): Show |
2 | a0001c0001t0004g0218 a0001c0002t0004g0136 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.422-1945_422-1944i others(17): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTCTT others(9): Show |
1 | a0001c0001t0004g0189 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.422-1945_422-1944i others(18): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0003g0202 a0001c0001t0003g0217 a0001c0002t0003g0063 |
3 | HG02735.hp1 HG03041.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.422-1955_422-1945d others(13): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(5): Show |
14 | a0001c0001t0003g0030 a0001c0001t0003g0182 a0001c0001t0003g0183 others(11): Show |
15 | HG00323.hp2 HG01168.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.422-1956_422-1945d others(14): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(6): Show |
19 | a0001c0001t0003g0029 a0001c0001t0003g0181 a0001c0001t0003g0184 others(16): Show |
21 | HG00140.hp1 HG00642.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.422-1957_422-1945d others(15): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0003g0152 a0001c0001t0003g0198 a0001c0001t0003g0227 others(9): Show |
13 | HG00597.hp1 HG01175.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-1958_422-1945d others(16): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0003g0293 a0001c0001t0005g0161 a0001c0001t0005g0170 others(2): Show |
5 | HG01071.hp1 HG01099.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.422-1959_422-1945d others(17): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(9): Show |
7 | a0001c0001t0003g0234 a0001c0001t0005g0160 a0001c0001t0005g0323 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-1960_422-1945d others(18): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0005g0159 a0001c0002t0005g0090 |
2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.422-1961_422-1945d others(19): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0253 a0001c0002t0005g0137 |
2 | HG02809.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.422-1962_422-1945d others(20): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0040 a0001c0001t0003g0272 |
3 | NA18967.hp2 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.422-1963_422-1945d others(21): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(13): Show |
3 | a0001c0001t0003g0273 a0001c0001t0005g0168 a0001c0002t0005g0132 |
3 | HG02630.hp1 HG03195.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.422-1964_422-1945d others(22): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | CTTTTTTT others(14): Show |
2 | a0001c0002t0003g0118 a0001c0002t0005g0139 |
2 | HG02559.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.422-1965_422-1945d others(23): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | C | T | 1 | a0001c0002t0004g0142 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.422-1944G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | CTTTT | C | 95 | a0001c0001t0001g0166 a0001c0001t0002g0007 a0001c0001t0002g0014 others(92): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.422-1948_422-1945d others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497568 | CTTTTT | C | 23 | a0001c0001t0002g0162 a0001c0001t0002g0238 a0001c0001t0002g0252 others(20): Show |
30 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.422-1949_422-1945d others(7): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497568 | |||||||
| chr4:174497572 | T | C | 3 | a0001c0001t0007g0186 a0001c0002t0002g0119 a0003c0006t0002g0050 |
3 | HG02071.hp1 HG02922.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.422-1948A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497572 | |||||||
| chr4:174497573 | T | C | 89 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(86): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.422-1949A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497573 | |||||||
| chr4:174497574 | T | C | 8 | a0001c0001t0002g0162 a0001c0001t0002g0238 a0001c0001t0002g0252 others(5): Show |
9 | HG02056.hp1 HG02965.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-1950A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497574 | |||||||
| chr4:174497575 | T | C | 1 | a0001c0002t0005g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.422-1951A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497575 | |||||||
| chr4:174497576 | T | C | 4 | a0001c0001t0001g0166 a0001c0002t0001g0106 a0001c0002t0001g0140 others(1): Show |
4 | HG01081.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-1952A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497576 | |||||||
| chr4:174497577 | T | C | 1 | a0001c0001t0011g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.422-1953A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497577 | |||||||
| chr4:174497578 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.422-1954A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497578 | |||||||
| chr4:174497628 | A | G | 100 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(97): Show |
137 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.422-2004T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497628 | |||||||
| chr4:174497704 | A | G | 18 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(15): Show |
18 | HG01123.hp2 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.422-2080T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497704 | |||||||
| chr4:174497860 | G | A | 1 | a0001c0003t0001g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.422-2236C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497860 | |||||||
| chr4:174497913 | T | C | 1 | a0001c0002t0003g0114 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.422-2289A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497913 | |||||||
| chr4:174497920 | G | A | 12 | a0001c0001t0004g0027 a0001c0001t0004g0171 a0001c0001t0004g0189 others(9): Show |
13 | HG00639.hp1 HG01891.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-2296C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174497920 | |||||||
| chr4:174498218 | G | T | 96 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(93): Show |
133 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.422-2594C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498218 | |||||||
| chr4:174498294 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0002t0001g0128 |
4 | HG01891.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-2670G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498294 | |||||||
| chr4:174498321 | A | AT | 100 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(97): Show |
137 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.422-2698dupA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498321 | |||||||
| chr4:174498443 | T | C | 2 | a0001c0002t0005g0092 a0001c0002t0005g0134 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.422-2819A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498443 | |||||||
| chr4:174498674 | AT | A | 12 | a0001c0001t0005g0170 a0001c0003t0001g0164 a0001c0003t0001g0167 others(9): Show |
12 | HG01123.hp2 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-3051delA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498674 | |||||||
| chr4:174498715 | GT | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.422-3092delA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498715 | |||||||
| chr4:174498868 | G | A | 1 | a0001c0001t0001g0013 | 3 | HG03688.hp1 HG03927.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.422-3244C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174498868 | |||||||
| chr4:174499017 | C | T | 11 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(8): Show |
13 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.422-3393G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499017 | |||||||
| chr4:174499125 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.422-3501C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499125 | |||||||
| chr4:174499244 | A | T | 7 | a0001c0001t0005g0170 a0001c0003t0001g0164 a0001c0003t0001g0167 others(4): Show |
7 | HG01123.hp2 HG02622.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-3620T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499244 | |||||||
| chr4:174499262 | G | A | 24 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0177 others(21): Show |
28 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.422-3638C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499262 | |||||||
| chr4:174499372 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
161 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.422-3748A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499372 | |||||||
| chr4:174499456 | T | C | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.422-3832A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499456 | |||||||
| chr4:174499611 | C | T | 1 | a0001c0001t0002g0041 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.422-3987G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499611 | |||||||
| chr4:174499676 | C | T | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-4052G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499676 | |||||||
| chr4:174499731 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.422-4107T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499731 | |||||||
| chr4:174499960 | G | GAC | 8 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(5): Show |
8 | HG02109.hp2 HG02717.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-4338_422-4337d others(4): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499960 | |||||||
| chr4:174499960 | G | GACAC | 93 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(90): Show |
130 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.422-4340_422-4337d others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499960 | |||||||
| chr4:174499960 | G | GACACAC | 3 | a0001c0001t0002g0229 a0001c0001t0002g0239 a0001c0001t0006g0321 |
3 | HG00609.hp1 HG02523.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.422-4342_422-4337d others(8): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174499960 | |||||||
| chr4:174500104 | G | A | 17 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(14): Show |
17 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.422-4480C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500104 | |||||||
| chr4:174500115 | G | A | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-4491C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500115 | |||||||
| chr4:174500149 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(224): Show |
297 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.422-4525C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500149 | |||||||
| chr4:174500288 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.422-4664C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500288 | |||||||
| chr4:174500307 | G | A | 2 | a0001c0001t0002g0190 a0001c0002t0002g0019 |
3 | HG03704.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.422-4683C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500307 | |||||||
| chr4:174500313 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
149 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.422-4689T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500313 | |||||||
| chr4:174500331 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.422-4707T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500331 | |||||||
| chr4:174500408 | C | G | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-4784G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500408 | |||||||
| chr4:174500449 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.422-4825C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500449 | |||||||
| chr4:174500486 | G | A | 12 | a0001c0001t0005g0170 a0001c0003t0001g0164 a0001c0003t0001g0167 others(9): Show |
12 | HG01123.hp2 HG01884.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.422-4862C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500486 | |||||||
| chr4:174500819 | T | C | 1 | a0001c0002t0001g0058 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.422-5195A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500819 | |||||||
| chr4:174500847 | T | C | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-5223A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500847 | |||||||
| chr4:174500891 | T | C | 8 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(5): Show |
10 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.422-5267A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174500891 | |||||||
| chr4:174501045 | C | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
285 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.422-5421G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501045 | |||||||
| chr4:174501138 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
333 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(330): Show |
intron_variant | MODIFIER | c.422-5514C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501138 | |||||||
| chr4:174501326 | T | C | 1 | a0001c0001t0007g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.422-5702A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501326 | |||||||
| chr4:174501371 | G | A | 1 | a0001c0002t0003g0082 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.422-5747C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501371 | |||||||
| chr4:174501550 | C | G | 3 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0252 |
3 | HG02965.hp1 HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.422-5926G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501550 | |||||||
| chr4:174501550 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.422-5926G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501550 | |||||||
| chr4:174501584 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.422-5960G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501584 | |||||||
| chr4:174501704 | A | G | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.422-6080T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501704 | |||||||
| chr4:174501705 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0209 a0001c0001t0001g0243 others(3): Show |
7 | HG00738.hp1 HG00741.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.422-6081A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501705 | |||||||
| chr4:174501745 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.422-6121C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501745 | |||||||
| chr4:174501850 | A | C | 10 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0178 others(7): Show |
12 | HG00642.hp2 HG01192.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-6226T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501850 | |||||||
| chr4:174501871 | T | C | 1 | a0001c0003t0001g0266 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-6247A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501871 | |||||||
| chr4:174501937 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
149 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.422-6313C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501937 | |||||||
| chr4:174501953 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(28): Show |
47 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.422-6329G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174501953 | |||||||
| chr4:174502027 | T | C | 91 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(88): Show |
126 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.422-6403A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502027 | |||||||
| chr4:174502028 | T | C | 4 | a0001c0001t0001g0166 a0001c0002t0001g0106 a0001c0002t0001g0140 others(1): Show |
4 | HG01081.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-6404A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502028 | |||||||
| chr4:174502120 | T | C | 2 | a0001c0001t0004g0218 a0001c0001t0004g0219 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.422-6496A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502120 | |||||||
| chr4:174502137 | CCAA | C | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-6516_422-6514d others(5): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502137 | |||||||
| chr4:174502346 | C | T | 2 | a0001c0001t0002g0179 a0001c0001t0002g0191 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.421+6350G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502346 | |||||||
| chr4:174502358 | G | A | 1 | a0001c0001t0003g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+6338C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502358 | |||||||
| chr4:174502414 | G | C | 1 | a0001c0001t0007g0303 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421+6282C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502414 | |||||||
| chr4:174502474 | G | T | 1 | a0001c0001t0003g0231 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.421+6222C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502474 | |||||||
| chr4:174502476 | T | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0033 others(48): Show |
63 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.421+6220A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502476 | |||||||
| chr4:174502480 | C | A | 1 | a0001c0001t0002g0305 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.421+6216G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502480 | |||||||
| chr4:174502506 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.421+6190C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502506 | |||||||
| chr4:174502535 | A | G | 1 | a0001c0002t0002g0060 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.421+6161T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502535 | |||||||
| chr4:174502561 | T | C | 8 | a0001c0001t0006g0017 a0001c0002t0005g0137 a0001c0002t0006g0093 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.421+6135A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502561 | |||||||
| chr4:174502582 | G | T | 2 | a0001c0001t0006g0017 a0001c0002t0006g0093 |
4 | HG01109.hp1 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+6114C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502582 | |||||||
| chr4:174502604 | A | G | 90 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(87): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+6092T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502604 | |||||||
| chr4:174502604 | A | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
201 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.421+6092T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502604 | |||||||
| chr4:174502605 | A | G | 90 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(87): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+6091T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502605 | |||||||
| chr4:174502634 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.421+6062G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502634 | |||||||
| chr4:174502639 | C | A | 90 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(87): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+6057G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502639 | |||||||
| chr4:174502641 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0033 others(47): Show |
62 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.421+6055C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502641 | |||||||
| chr4:174502677 | C | CA | 31 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(28): Show |
33 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.421+6018dupT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502677 | |||||||
| chr4:174502677 | C | CAAA | 86 | a0001c0001t0001g0037 a0001c0001t0001g0209 a0001c0001t0001g0288 others(83): Show |
121 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.421+6016_421+6018d others(5): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502677 | |||||||
| chr4:174502677 | C | CAAAA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(106): Show |
141 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.421+6015_421+6018d others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502677 | |||||||
| chr4:174502677 | C | CAAAAA | 20 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0001t0001g0180 others(17): Show |
22 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.421+6014_421+6018d others(7): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502677 | |||||||
| chr4:174502677 | CA | C | 5 | a0001c0001t0003g0008 a0001c0001t0003g0182 a0001c0001t0003g0254 others(2): Show |
8 | HG02135.hp2 HG03239.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.421+6018delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502677 | |||||||
| chr4:174502684 | A | G | 1 | a0001c0001t0003g0254 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.421+6012T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502684 | |||||||
| chr4:174502732 | A | G | 1 | a0001c0001t0011g0312 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.421+5964T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502732 | |||||||
| chr4:174502964 | C | T | 1 | a0001c0002t0003g0071 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.421+5732G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174502964 | |||||||
| chr4:174503021 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
114 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.421+5675C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503021 | |||||||
| chr4:174503152 | G | T | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+5544C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503152 | |||||||
| chr4:174503417 | G | A | 1 | a0001c0002t0003g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.421+5279C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503417 | |||||||
| chr4:174503532 | C | T | 1 | a0001c0001t0007g0186 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.421+5164G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503532 | |||||||
| chr4:174503548 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.421+5148C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503548 | |||||||
| chr4:174503651 | T | C | 10 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(7): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+5045A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503651 | |||||||
| chr4:174503719 | AT | A | 43 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0177 others(40): Show |
47 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.421+4976delA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503719 | |||||||
| chr4:174503772 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.421+4924C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503772 | |||||||
| chr4:174503911 | A | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(32): Show |
51 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.421+4785T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174503911 | |||||||
| chr4:174504020 | G | A | 30 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0036 others(27): Show |
39 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.421+4676C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504020 | |||||||
| chr4:174504105 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(28): Show |
47 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.421+4591C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504105 | |||||||
| chr4:174504468 | T | C | 12 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(9): Show |
14 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+4228A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504468 | |||||||
| chr4:174504535 | T | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0246 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.421+4161A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504535 | |||||||
| chr4:174504637 | G | A | 1 | a0001c0001t0007g0303 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421+4059C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504637 | |||||||
| chr4:174504653 | C | CA | 11 | a0001c0001t0002g0240 a0001c0001t0005g0159 a0001c0001t0005g0160 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.421+4042dupT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504653 | |||||||
| chr4:174504653 | C | T | 3 | a0001c0001t0004g0047 a0001c0001t0004g0330 a0001c0002t0004g0129 |
4 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+4043G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504653 | |||||||
| chr4:174504653 | CA | C | 12 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(9): Show |
14 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.421+4042delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504653 | |||||||
| chr4:174504674 | G | A | 11 | a0001c0001t0005g0170 a0001c0003t0001g0164 a0001c0003t0001g0167 others(8): Show |
11 | HG01123.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+4022C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504674 | |||||||
| chr4:174504701 | T | A | 1 | a0001c0001t0005g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.421+3995A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504701 | |||||||
| chr4:174504739 | A | G | 13 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(10): Show |
15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+3957T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504739 | |||||||
| chr4:174504748 | GGTT | G | 3 | a0001c0003t0001g0261 a0001c0003t0001g0264 a0005c0009t0001g0123 |
3 | HG02486.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.421+3945_421+3947d others(5): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504748 | |||||||
| chr4:174504767 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
161 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.421+3929G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504767 | |||||||
| chr4:174504769 | C | A | 24 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0177 others(21): Show |
28 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.421+3927G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504769 | |||||||
| chr4:174504786 | C | T | 90 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(87): Show |
125 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.421+3910G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504786 | |||||||
| chr4:174504814 | A | AAAAC | 21 | a0001c0001t0002g0014 a0001c0001t0002g0042 a0001c0001t0002g0193 others(18): Show |
27 | HG00140.hp2 HG00438.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.421+3878_421+3881d others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174504814 | A | AAAACAAA others(1): Show |
4 | a0001c0001t0002g0038 a0001c0001t0002g0187 a0001c0001t0002g0201 others(1): Show |
7 | HG01081.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.421+3874_421+3881d others(10): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174504814 | AAAAC | A | 73 | a0001c0001t0001g0166 a0001c0001t0001g0212 a0001c0001t0001g0242 others(70): Show |
81 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.421+3878_421+3881d others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174504814 | AAAACAAA others(1): Show |
A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0033 others(96): Show |
118 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.421+3874_421+3881d others(10): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174504814 | AAAACAAA others(5): Show |
A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(31): Show |
50 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.421+3870_421+3881d others(14): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174504814 | AAAACAAA others(9): Show |
A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0002t0001g0128 |
4 | HG01891.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+3866_421+3881d others(18): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174504814 | |||||||
| chr4:174505004 | T | C | 4 | a0001c0001t0001g0292 a0001c0002t0001g0097 a0001c0002t0001g0098 others(1): Show |
4 | HG00735.hp1 HG01255.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+3692A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505004 | |||||||
| chr4:174505318 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.421+3378T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505318 | |||||||
| chr4:174505521 | A | T | 2 | a0003c0006t0002g0050 a0003c0007t0002g0236 |
2 | NA18978.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.421+3175T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505521 | |||||||
| chr4:174505575 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.421+3121A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505575 | |||||||
| chr4:174505634 | ACAAGG | A | 9 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+3057_421+3061d others(7): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505634 | |||||||
| chr4:174505774 | C | T | 11 | a0001c0001t0005g0170 a0001c0003t0001g0164 a0001c0003t0001g0167 others(8): Show |
11 | HG01123.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.421+2922G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505774 | |||||||
| chr4:174505888 | T | C | 20 | a0001c0001t0004g0047 a0001c0001t0004g0330 a0001c0001t0005g0155 others(17): Show |
21 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.421+2808A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505888 | |||||||
| chr4:174505926 | A | C | 4 | a0001c0001t0003g0217 a0001c0001t0007g0154 a0001c0001t0007g0214 others(1): Show |
4 | HG03041.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+2770T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174505926 | |||||||
| chr4:174506060 | A | G | 1 | a0001c0001t0003g0253 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.421+2636T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506060 | |||||||
| chr4:174506091 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
312 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.421+2605A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506091 | |||||||
| chr4:174506100 | C | G | 13 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(10): Show |
15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.421+2596G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506100 | |||||||
| chr4:174506173 | C | A | 1 | a0001c0001t0002g0311 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.421+2523G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506173 | |||||||
| chr4:174506573 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.421+2123G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506573 | |||||||
| chr4:174506640 | G | T | 1 | a0001c0001t0006g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.421+2056C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506640 | |||||||
| chr4:174506703 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.421+1993T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506703 | |||||||
| chr4:174506816 | G | C | 1 | a0001c0003t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421+1880C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506816 | |||||||
| chr4:174506956 | A | G | 10 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(7): Show |
12 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.421+1740T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174506956 | |||||||
| chr4:174507157 | T | C | 54 | a0001c0001t0002g0153 a0001c0001t0002g0162 a0001c0001t0002g0211 others(51): Show |
58 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.421+1539A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507157 | |||||||
| chr4:174507158 | G | A | 5 | a0001c0002t0005g0090 a0001c0002t0005g0091 a0001c0002t0005g0092 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+1538C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507158 | |||||||
| chr4:174507168 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
213 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.421+1528G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507168 | |||||||
| chr4:174507224 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.421+1472C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507224 | |||||||
| chr4:174507547 | T | C | 22 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(19): Show |
22 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.421+1149A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507547 | |||||||
| chr4:174507548 | G | A | 17 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(14): Show |
17 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.421+1148C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507548 | |||||||
| chr4:174507552 | T | C | 23 | a0001c0001t0005g0155 a0001c0001t0005g0159 a0001c0001t0005g0160 others(20): Show |
23 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.421+1144A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507552 | |||||||
| chr4:174507579 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
132 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.421+1117A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507579 | |||||||
| chr4:174507581 | A | C | 26 | a0001c0001t0001g0165 a0001c0001t0001g0174 a0001c0001t0001g0177 others(23): Show |
31 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.421+1115T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507581 | |||||||
| chr4:174507741 | G | A | 1 | a0001c0001t0002g0287 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.421+955C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507741 | |||||||
| chr4:174507820 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.421+876T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507820 | |||||||
| chr4:174507860 | T | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0287 |
2 | NA18970.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.421+836A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507860 | |||||||
| chr4:174507954 | C | T | 2 | a0001c0001t0003g0217 a0001c0001t0007g0214 |
2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.421+742G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174507954 | |||||||
| chr4:174508036 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.421+660T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508036 | |||||||
| chr4:174508062 | C | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.421+634G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508062 | |||||||
| chr4:174508182 | A | G | 3 | a0001c0001t0003g0234 a0001c0002t0003g0131 a0001c0002t0003g0135 |
3 | HG02717.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.421+514T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508182 | |||||||
| chr4:174508219 | GT | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
305 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.421+476delA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508219 | |||||||
| chr4:174508310 | C | T | 1 | a0001c0003t0001g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.421+386G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508310 | |||||||
| chr4:174508657 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0033 others(144): Show |
197 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.421+39C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 4/6 | chr4 | 174508657 | |||||||
| chr4:174508935 | T | C | 2 | a0001c0001t0001g0180 a0001c0002t0003g0094 |
2 | HG00323.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.325-143A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174508935 | |||||||
| chr4:174508944 | T | C | 1 | a0001c0001t0006g0321 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.325-152A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174508944 | |||||||
| chr4:174509039 | T | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(55): Show |
76 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.325-247A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509039 | |||||||
| chr4:174509089 | A | T | 3 | a0001c0001t0002g0260 a0001c0001t0003g0262 a0001c0003t0001g0261 |
3 | HG03516.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-297T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509089 | |||||||
| chr4:174509127 | A | G | 26 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0001t0001g0165 others(23): Show |
27 | HG00323.hp2 HG01081.hp1 HG01358.hp1 others(24): Show |
intron_variant | MODIFIER | c.325-335T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509127 | |||||||
| chr4:174509137 | T | G | 113 | a0001c0001t0001g0151 a0001c0001t0001g0172 a0001c0001t0001g0177 others(110): Show |
143 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.325-345A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509137 | |||||||
| chr4:174509145 | T | A | 1 | a0001c0001t0001g0313 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.325-353A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509145 | |||||||
| chr4:174509497 | C | G | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-705G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509497 | |||||||
| chr4:174509521 | T | C | 8 | a0001c0001t0002g0031 a0001c0001t0002g0201 a0001c0001t0003g0197 others(5): Show |
9 | HG00140.hp1 HG01168.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.325-729A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509521 | |||||||
| chr4:174509535 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.325-743T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509535 | |||||||
| chr4:174509906 | C | T | 1 | a0001c0001t0002g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.325-1114G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509906 | |||||||
| chr4:174509910 | CA | C | 18 | a0001c0001t0001g0151 a0001c0001t0001g0177 a0001c0002t0001g0006 others(15): Show |
22 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.325-1119delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509910 | |||||||
| chr4:174509923 | G | A | 1 | a0001c0003t0001g0266 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.325-1131C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509923 | |||||||
| chr4:174509923 | GA | G | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(20): Show |
25 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.325-1132delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509923 | |||||||
| chr4:174509924 | A | G | 1 | a0001c0003t0001g0266 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.325-1132T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509924 | |||||||
| chr4:174509952 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.325-1160T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174509952 | |||||||
| chr4:174510124 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.325-1332T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510124 | |||||||
| chr4:174510154 | T | A | 1 | a0001c0001t0001g0292 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-1362A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510154 | |||||||
| chr4:174510268 | AT | A | 73 | a0001c0001t0002g0211 a0001c0001t0002g0221 a0001c0001t0002g0260 others(70): Show |
97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.325-1477delA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510268 | |||||||
| chr4:174510337 | A | G | 9 | a0001c0001t0001g0033 a0001c0001t0002g0211 a0001c0001t0002g0221 others(6): Show |
10 | HG00597.hp1 HG00609.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-1545T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510337 | |||||||
| chr4:174510462 | T | C | 4 | a0001c0002t0005g0090 a0001c0002t0005g0091 a0001c0002t0005g0092 others(1): Show |
4 | HG02258.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-1670A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510462 | |||||||
| chr4:174510471 | C | T | 1 | a0001c0001t0003g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.325-1679G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510471 | |||||||
| chr4:174510512 | T | A | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(20): Show |
25 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.325-1720A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510512 | |||||||
| chr4:174510518 | G | A | 1 | a0001c0002t0005g0108 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.325-1726C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510518 | |||||||
| chr4:174510771 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.325-1979T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510771 | |||||||
| chr4:174510823 | T | C | 1 | a0001c0002t0001g0023 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.325-2031A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510823 | |||||||
| chr4:174510884 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.325-2092C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510884 | |||||||
| chr4:174510997 | A | G | 3 | a0001c0001t0002g0260 a0001c0001t0003g0262 a0001c0003t0001g0261 |
3 | HG03516.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.325-2205T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174510997 | |||||||
| chr4:174511030 | C | G | 1 | a0001c0001t0002g0041 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.325-2238G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511030 | |||||||
| chr4:174511148 | C | G | 23 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(20): Show |
25 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.325-2356G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511148 | |||||||
| chr4:174511215 | GA | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
202 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.325-2424delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511215 | |||||||
| chr4:174511215 | GAA | G | 65 | a0001c0001t0001g0286 a0001c0001t0003g0280 a0001c0002t0001g0021 others(62): Show |
89 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.325-2425_325-2424d others(4): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511215 | |||||||
| chr4:174511340 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.325-2548A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511340 | |||||||
| chr4:174511371 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(46): Show |
66 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.325-2579A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511371 | |||||||
| chr4:174511380 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.325-2588A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511380 | |||||||
| chr4:174511604 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.325-2812A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511604 | |||||||
| chr4:174511647 | T | A | 1 | a0001c0001t0002g0281 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.325-2855A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511647 | |||||||
| chr4:174511683 | G | C | 1 | a0001c0002t0003g0084 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.325-2891C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511683 | |||||||
| chr4:174511739 | C | T | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.325-2947G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511739 | |||||||
| chr4:174511766 | C | T | 1 | a0001c0001t0002g0041 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.325-2974G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511766 | |||||||
| chr4:174511794 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.325-3002G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511794 | |||||||
| chr4:174511804 | G | T | 72 | a0001c0001t0002g0211 a0001c0001t0002g0221 a0001c0001t0002g0260 others(69): Show |
96 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.325-3012C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511804 | |||||||
| chr4:174511807 | C | T | 8 | a0001c0001t0003g0263 a0001c0001t0004g0047 a0001c0001t0004g0330 others(5): Show |
11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.325-3015G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511807 | |||||||
| chr4:174511837 | G | T | 72 | a0001c0001t0002g0211 a0001c0001t0002g0221 a0001c0001t0002g0260 others(69): Show |
96 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.325-3045C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511837 | |||||||
| chr4:174511846 | T | C | 22 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(19): Show |
26 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.325-3054A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511846 | |||||||
| chr4:174511942 | G | A | 2 | a0001c0002t0005g0139 a0001c0005t0009g0138 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.325-3150C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174511942 | |||||||
| chr4:174512032 | T | C | 1 | a0001c0001t0008g0039 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.325-3240A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512032 | |||||||
| chr4:174512101 | G | A | 2 | a0001c0002t0004g0124 a0001c0002t0004g0125 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.325-3309C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512101 | |||||||
| chr4:174512145 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0213 others(6): Show |
14 | HG00423.hp2 HG00544.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.325-3353C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512145 | |||||||
| chr4:174512187 | A | C | 62 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0163 others(59): Show |
69 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.325-3395T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512187 | |||||||
| chr4:174512265 | C | G | 3 | a0001c0001t0003g0263 a0001c0001t0004g0047 a0001c0001t0004g0330 |
4 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.325-3473G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512265 | |||||||
| chr4:174512320 | C | G | 1 | a0001c0001t0001g0290 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.325-3528G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512320 | |||||||
| chr4:174512558 | C | T | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-3766G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512558 | |||||||
| chr4:174512569 | T | C | 17 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(14): Show |
21 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.325-3777A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512569 | |||||||
| chr4:174512762 | G | T | 22 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(19): Show |
26 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.325-3970C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512762 | |||||||
| chr4:174512845 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.325-4053A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512845 | |||||||
| chr4:174512850 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.325-4058A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512850 | |||||||
| chr4:174512923 | C | T | 17 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(14): Show |
21 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.325-4131G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174512923 | |||||||
| chr4:174513011 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.325-4219G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513011 | |||||||
| chr4:174513108 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.325-4316T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513108 | |||||||
| chr4:174513243 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(61): Show |
84 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.325-4451T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513243 | |||||||
| chr4:174513313 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.325-4521C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513313 | |||||||
| chr4:174513369 | A | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(61): Show |
84 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.325-4577T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513369 | |||||||
| chr4:174513428 | GGTATCCT others(4): Show |
G | 1 | a0001c0001t0003g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.324+4532_324+4542d others(13): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513428 | |||||||
| chr4:174513460 | A | AT | 26 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(23): Show |
29 | HG00609.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.324+4510dupA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513460 | |||||||
| chr4:174513565 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.324+4406T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513565 | |||||||
| chr4:174513627 | G | A | 1 | a0001c0002t0002g0085 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.324+4344C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513627 | |||||||
| chr4:174513650 | G | C | 22 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(19): Show |
24 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.324+4321C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513650 | |||||||
| chr4:174513698 | A | G | 22 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(19): Show |
24 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.324+4273T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513698 | |||||||
| chr4:174513703 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.324+4268C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513703 | |||||||
| chr4:174513803 | G | T | 16 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(13): Show |
20 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.324+4168C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513803 | |||||||
| chr4:174513852 | T | A | 21 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(18): Show |
23 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+4119A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174513852 | |||||||
| chr4:174514205 | A | C | 1 | a0001c0002t0002g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.324+3766T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514205 | |||||||
| chr4:174514242 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.324+3729G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514242 | |||||||
| chr4:174514459 | C | A | 1 | a0001c0002t0003g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.324+3512G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514459 | |||||||
| chr4:174514507 | T | C | 21 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(18): Show |
23 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.324+3464A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514507 | |||||||
| chr4:174514589 | G | A | 1 | a0001c0002t0002g0086 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.324+3382C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514589 | |||||||
| chr4:174514609 | A | G | 1 | a0001c0001t0005g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+3362T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514609 | |||||||
| chr4:174514809 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+3162A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514809 | |||||||
| chr4:174514866 | C | T | 1 | a0001c0001t0002g0287 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.324+3105G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174514866 | |||||||
| chr4:174515120 | C | T | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0203 others(2): Show |
5 | HG00738.hp2 HG02602.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.324+2851G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515120 | |||||||
| chr4:174515297 | A | G | 8 | a0001c0001t0002g0252 a0001c0002t0001g0145 a0001c0002t0001g0146 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+2674T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515297 | |||||||
| chr4:174515309 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.324+2662T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515309 | |||||||
| chr4:174515316 | T | C | 1 | a0001c0001t0005g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+2655A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515316 | |||||||
| chr4:174515355 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.324+2616C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515355 | |||||||
| chr4:174515356 | C | G | 1 | a0001c0001t0001g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.324+2615G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515356 | |||||||
| chr4:174515401 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0221 a0001c0001t0003g0247 others(1): Show |
4 | HG01358.hp1 HG02683.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+2570C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515401 | |||||||
| chr4:174515458 | T | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(46): Show |
66 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.324+2513A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515458 | |||||||
| chr4:174515469 | T | C | 1 | a0001c0001t0005g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.324+2502A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515469 | |||||||
| chr4:174515540 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.324+2431C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515540 | |||||||
| chr4:174515617 | T | TAGAC | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
343 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.324+2353_324+2354i others(6): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515617 | |||||||
| chr4:174515622 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
322 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.324+2349C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515622 | |||||||
| chr4:174515630 | A | G | 1 | a0001c0002t0005g0126 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.324+2341T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515630 | |||||||
| chr4:174515735 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.324+2236G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515735 | |||||||
| chr4:174515837 | C | G | 2 | a0001c0001t0002g0215 a0001c0001t0003g0216 |
2 | NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.324+2134G>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515837 | |||||||
| chr4:174515872 | A | G | 3 | a0001c0002t0002g0054 a0001c0002t0002g0056 a0001c0002t0003g0055 |
3 | HG01346.hp2 HG01934.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.324+2099T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515872 | |||||||
| chr4:174515966 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0037 others(134): Show |
181 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.324+2005C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515966 | |||||||
| chr4:174515968 | A | C | 1 | a0001c0001t0007g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.324+2003T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174515968 | |||||||
| chr4:174516229 | C | T | 7 | a0001c0001t0002g0256 a0001c0001t0002g0281 a0001c0001t0002g0287 others(4): Show |
10 | HG02074.hp2 NA18942.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+1742G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516229 | |||||||
| chr4:174516275 | C | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.324+1696G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516275 | |||||||
| chr4:174516302 | C | T | 17 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(14): Show |
21 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.324+1669G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516302 | |||||||
| chr4:174516310 | T | TA | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
299 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.324+1660dupT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516310 | |||||||
| chr4:174516379 | T | A | 1 | a0001c0001t0002g0211 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.324+1592A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516379 | |||||||
| chr4:174516462 | C | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(84): Show |
113 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.324+1509G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516462 | |||||||
| chr4:174516470 | C | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(84): Show |
113 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.324+1501G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516470 | |||||||
| chr4:174516512 | G | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.324+1459C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516512 | |||||||
| chr4:174516520 | A | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(60): Show |
87 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.324+1451T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516520 | |||||||
| chr4:174516688 | C | T | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1283G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516688 | |||||||
| chr4:174516736 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
85 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.324+1235A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516736 | |||||||
| chr4:174516741 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
85 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.324+1230G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516741 | |||||||
| chr4:174516915 | G | A | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1056C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516915 | |||||||
| chr4:174516986 | G | A | 3 | a0001c0001t0005g0323 a0001c0001t0005g0324 a0001c0008t0005g0322 |
3 | HG03139.hp1 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.324+985C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174516986 | |||||||
| chr4:174517000 | G | A | 1 | a0001c0002t0005g0137 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.324+971C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517000 | |||||||
| chr4:174517102 | G | A | 2 | a0001c0001t0002g0153 a0001c0001t0003g0152 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.324+869C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517102 | |||||||
| chr4:174517307 | TTTCAGGA others(22): Show |
T | 1 | a0001c0001t0001g0283 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.324+635_324+663del others(29): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517307 | |||||||
| chr4:174517341 | C | T | 3 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | NA18970.hp1 NA19062.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.324+630G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517341 | |||||||
| chr4:174517382 | T | G | 1 | a0001c0001t0003g0247 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.324+589A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517382 | |||||||
| chr4:174517467 | T | C | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+504A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517467 | |||||||
| chr4:174517577 | G | A | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+394C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517577 | |||||||
| chr4:174517643 | A | G | 5 | a0001c0001t0005g0323 a0001c0001t0005g0324 a0001c0001t0006g0017 others(2): Show |
7 | HG01109.hp1 HG02145.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+328T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517643 | |||||||
| chr4:174517671 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.324+300A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517671 | |||||||
| chr4:174517726 | C | A | 1 | a0001c0001t0003g0202 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.324+245G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517726 | |||||||
| chr4:174517905 | T | C | 8 | a0001c0001t0003g0263 a0001c0001t0004g0047 a0001c0001t0004g0330 others(5): Show |
11 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.324+66A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 3/6 | chr4 | 174517905 | |||||||
| chr4:174518119 | C | A | 5 | a0001c0001t0001g0248 a0001c0001t0001g0251 a0001c0001t0002g0014 others(2): Show |
7 | HG02027.hp1 NA18944.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.218-42G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518119 | |||||||
| chr4:174518199 | A | T | 2 | a0001c0002t0004g0124 a0001c0002t0004g0125 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.218-122T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518199 | |||||||
| chr4:174518240 | T | C | 3 | a0001c0001t0002g0252 a0001c0002t0005g0139 a0001c0005t0009g0138 |
3 | HG01884.hp2 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.218-163A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518240 | |||||||
| chr4:174518247 | A | T | 16 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0172 others(13): Show |
18 | HG01123.hp2 HG01884.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.218-170T>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518247 | |||||||
| chr4:174518515 | C | T | 2 | a0001c0002t0005g0139 a0001c0005t0009g0138 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.218-438G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518515 | |||||||
| chr4:174518845 | G | T | 23 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0001c0001t0002g0162 others(20): Show |
24 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.218-768C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518845 | |||||||
| chr4:174518873 | C | T | 16 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0023 others(13): Show |
20 | HG00323.hp2 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.218-796G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518873 | |||||||
| chr4:174518874 | G | T | 2 | a0001c0002t0005g0139 a0001c0005t0009g0138 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.218-797C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518874 | |||||||
| chr4:174518944 | T | C | 4 | a0001c0002t0005g0090 a0001c0002t0005g0091 a0001c0002t0005g0092 others(1): Show |
4 | HG02258.hp1 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-867A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518944 | |||||||
| chr4:174518990 | TA | T | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-914delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174518990 | |||||||
| chr4:174519114 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(69): Show |
93 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.218-1037A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519114 | |||||||
| chr4:174519218 | A | AT | 52 | a0001c0001t0001g0026 a0001c0001t0001g0151 a0001c0001t0001g0163 others(49): Show |
55 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(52): Show |
intron_variant | MODIFIER | c.218-1142dupA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519218 | |||||||
| chr4:174519218 | A | ATT | 67 | a0001c0001t0002g0260 a0001c0001t0003g0262 a0001c0001t0003g0280 others(64): Show |
91 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.218-1143_218-1142d others(4): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519218 | |||||||
| chr4:174519218 | A | ATTT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(69): Show |
93 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.218-1144_218-1142d others(5): Show |
HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519218 | |||||||
| chr4:174519236 | C | T | 69 | a0001c0001t0002g0260 a0001c0001t0003g0262 a0001c0001t0003g0280 others(66): Show |
93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.218-1159G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519236 | |||||||
| chr4:174519302 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0003g0152 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.218-1225G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519302 | |||||||
| chr4:174519363 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.218-1286T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519363 | |||||||
| chr4:174519371 | G | A | 12 | a0001c0001t0001g0151 a0001c0001t0001g0319 a0001c0001t0001g0320 others(9): Show |
16 | HG00741.hp1 HG01099.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.218-1294C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519371 | |||||||
| chr4:174519430 | A | G | 6 | a0001c0001t0002g0211 a0001c0001t0005g0323 a0001c0001t0005g0324 others(3): Show |
8 | HG01109.hp1 HG02145.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-1353T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519430 | |||||||
| chr4:174519487 | T | G | 2 | a0001c0002t0005g0139 a0001c0005t0009g0138 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.218-1410A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519487 | |||||||
| chr4:174519759 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.218-1682G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519759 | |||||||
| chr4:174519761 | A | C | 1 | a0001c0001t0003g0210 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.218-1684T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519761 | |||||||
| chr4:174519769 | T | C | 4 | a0001c0001t0001g0203 a0001c0002t0001g0140 a0001c0002t0001g0141 others(1): Show |
4 | HG01081.hp1 HG02602.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-1692A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519769 | |||||||
| chr4:174519776 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.218-1699A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174519776 | |||||||
| chr4:174520034 | A | G | 2 | a0001c0002t0004g0124 a0001c0002t0004g0125 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.217+1910T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520034 | |||||||
| chr4:174520087 | A | G | 1 | a0001c0001t0002g0158 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.217+1857T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520087 | |||||||
| chr4:174520144 | G | A | 6 | a0001c0001t0001g0207 a0001c0001t0002g0206 a0001c0001t0002g0208 others(3): Show |
6 | NA18951.hp1 NA18953.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+1800C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520144 | |||||||
| chr4:174520149 | A | G | 1 | a0001c0001t0016g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.217+1795T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520149 | |||||||
| chr4:174520222 | T | G | 1 | a0001c0001t0001g0286 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.217+1722A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520222 | |||||||
| chr4:174520223 | G | T | 1 | a0001c0001t0001g0286 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.217+1721C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520223 | |||||||
| chr4:174520246 | C | A | 1 | a0001c0001t0002g0259 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.217+1698G>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520246 | |||||||
| chr4:174520315 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.217+1629G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520315 | |||||||
| chr4:174520503 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.217+1441G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520503 | |||||||
| chr4:174520861 | C | T | 4 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+1083G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520861 | |||||||
| chr4:174520910 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(159): Show |
210 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.217+1034A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520910 | |||||||
| chr4:174520995 | T | C | 1 | a0001c0002t0003g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.217+949A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174520995 | |||||||
| chr4:174521022 | T | G | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+922A>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521022 | |||||||
| chr4:174521047 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(50): Show |
75 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.217+897T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521047 | |||||||
| chr4:174521154 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(58): Show |
86 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.217+790A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521154 | |||||||
| chr4:174521225 | C | CA | 45 | a0001c0001t0001g0151 a0001c0001t0001g0268 a0001c0001t0001g0277 others(42): Show |
46 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.217+718dupT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521225 | |||||||
| chr4:174521225 | CA | C | 20 | a0001c0001t0004g0156 a0001c0002t0001g0128 a0001c0002t0001g0130 others(17): Show |
20 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.217+718delT | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521225 | |||||||
| chr4:174521340 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0002t0001g0048 |
3 | HG00642.hp1 HG01515.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.217+604C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521340 | |||||||
| chr4:174521401 | T | A | 19 | a0001c0002t0001g0128 a0001c0002t0001g0130 a0001c0002t0001g0140 others(16): Show |
19 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.217+543A>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521401 | |||||||
| chr4:174521518 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.217+426T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521518 | |||||||
| chr4:174521618 | T | C | 2 | a0001c0002t0002g0119 a0001c0002t0003g0118 |
2 | HG02071.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.217+326A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521618 | |||||||
| chr4:174521649 | A | G | 1 | a0001c0001t0005g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.217+295T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521649 | |||||||
| chr4:174521671 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(55): Show |
82 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.217+273A>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521671 | |||||||
| chr4:174521750 | C | T | 1 | a0001c0001t0007g0154 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.217+194G>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521750 | |||||||
| chr4:174521772 | A | G | 2 | a0001c0001t0002g0153 a0001c0001t0003g0152 |
2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.217+172T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521772 | |||||||
| chr4:174521805 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.217+139T>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521805 | |||||||
| chr4:174521838 | G | C | 3 | a0001c0002t0001g0120 a0001c0002t0001g0121 a0001c0002t0001g0122 |
3 | NA18992.hp2 NA19000.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.217+106C>G | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 2/6 | chr4 | 174521838 | |||||||
| chr4:174522083 | G | A | 2 | a0001c0001t0004g0047 a0001c0001t0004g0330 |
3 | HG02055.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.94-16C>T | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 1/6 | chr4 | 174522083 | |||||||
| chr4:174522110 | G | T | 5 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0147 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.94-43C>A | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 1/6 | chr4 | 174522110 | |||||||
| chr4:174522171 | A | G | 19 | a0001c0002t0001g0128 a0001c0002t0001g0130 a0001c0002t0001g0140 others(16): Show |
19 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.94-104T>C | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 1/6 | chr4 | 174522171 | |||||||
| chr4:174522273 | C | CT | 88 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(85): Show |
116 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.93+85dupA | HPGD | ENSG00000164120.14 | transcript | ENST00000296522.11 | protein_coding | 1/6 | chr4 | 174522273 |