Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 94031 |
| ensemblid | ENSG00000170801.10 |
| hgncid | 30406 |
| symbol | HTRA3 |
| name | HtrA serine peptidase 3 |
| refseq_nuc | NM_053044.5 |
| refseq_prot | NP_444272.1 |
| ensembl_nuc | ENST00000307358.7 |
| ensembl_prot | ENSP00000303766.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 8269754 |
| end | 8307098 |
| strand | + |
| ver | v1.2 |
| region | chr4:8269754-8307098 |
| region5000 | chr4:8264754-8312098 |
| regionname0 | HTRA3_chr4_8269754_8307098 |
| regionname5000 | HTRA3_chr4_8264754_8312098 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 453 | 370 | 90 | 67 | 150 | 15 | 47 | 111 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0002 | 0/1 | 453 | 9 | 3 | 4 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0003 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0004 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0005 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0006 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0007 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0008 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0009 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| a0010 | 0/0 | 28 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(23): Show |
chr4 | 8264754 | 8312098 |
| a0011 | 0/0 | 453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | MQARA others(448): Show |
chr4 | 8264754 | 8312098 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1359 | 367 | 88 | 67 | 150 | 15 | 46 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0001c0005 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0001c0011 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0001c0014 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0002c0002 | 0/1 | 1359 | 9 | 3 | 4 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0003c0007 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0004c0008 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0005c0009 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0006c0006 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0007c0013 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0008c0012 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0009c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0010c0003 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 | ||
| a0011c0004 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | ATGCA others(1354): Show |
chr4 | 8264754 | 8312098 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2539 | 343 | 75 | 65 | 144 | 15 | 43 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0002 | 0/0 | 2539 | 3 | 3 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0003 | 0/0 | 2539 | 3 | 2 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0004 | 0/0 | 2539 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0005 | 0/0 | 2539 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0006 | 0/0 | 2539 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0007 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0008 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0010 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0011 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0012 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0013 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0014 | 0/0 | 2539 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0015 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0016 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0017 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0018 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0001t0019 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0005t0001 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0011t0001 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0001c0014t0001 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0002c0002t0001 | 0/1 | 2539 | 8 | 2 | 4 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0002c0002t0009 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0003c0007t0001 | 0/0 | 2539 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0004c0008t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0005c0009t0001 | 0/0 | 2539 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0006c0006t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0007c0013t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0008c0012t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0009c0010t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0010c0003t0001 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| a0011c0004t0001 | 0/0 | 2539 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | GTCAG others(2534): Show |
chr4 | 8264754 | 8312098 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0006g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0011g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0012g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0013g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0014g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0016g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0017g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0018g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0001t0019g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0001c0014t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0002c0002t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0003c0007t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0004c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0005c0009t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0006c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0007c0013t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0008c0012t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0009c0010t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0010c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| a0011c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0059 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | FIN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00642 | hp1 | a0001 | c0001 | t0014 | g0207 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01975 | hp2 | a0003 | c0007 | t0001 | g0326 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02132 | hp1 | a0004 | c0008 | t0001 | g0113 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0324 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0343 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0321 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0346 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02809 | hp2 | a0002 | c0002 | t0009 | g0061 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0176 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03209 | hp2 | a0005 | c0009 | t0001 | g0345 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0122 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03486 | hp1 | a0001 | c0014 | t0001 | g0344 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03669 | hp1 | a0001 | c0011 | t0001 | g0050 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04199 | hp1 | a0001 | c0001 | t0019 | g0248 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18967 | hp1 | a0001 | c0001 | t0006 | g0333 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0334 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18980 | hp1 | a0001 | c0001 | t0017 | g0352 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18982 | hp1 | a0006 | c0006 | t0001 | g0066 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18984 | hp1 | a0001 | c0001 | t0018 | g0249 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18990 | hp2 | a0007 | c0013 | t0001 | g0099 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA18999 | hp2 | a0008 | c0012 | t0001 | g0244 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19062 | hp2 | a0001 | c0001 | t0013 | g0114 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19067 | hp2 | a0009 | c0010 | t0001 | g0277 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19070 | hp1 | a0010 | c0003 | t0001 | g0297 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ASW | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ASW | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20905 | hp2 | a0011 | c0004 | t0001 | g0096 | SAS | GIH | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0088 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0133 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0073 | REF | REF | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0262 | REF | REF | HTRA3_chr4_8264754_8312098 | HTRA3 | chr4 | 8264754 | 8312098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:8270048 | C | G | 1 | a0002 | 8 | HG00140.hp1 HG00639.hp1 HG01074.hp1 others(5): Show |
missense_variant | MODERATE | c.80C>G | p.Ala27Gly | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 295/2539 | 80/1362 | 27/453 | chr4 | 8270048 | |||
| chr4:8270055 | C | A | 1 | a0010 | 1 | NA19070.hp1 | stop_gained | HIGH | c.87C>A | p.Cys29* | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 302/2539 | 87/1362 | 29/453 | chr4 | 8270055 | |||
| chr4:8270146 | G | A | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.178G>A | p.Glu60Lys | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 393/2539 | 178/1362 | 60/453 | chr4 | 8270146 | |||
| chr4:8291399 | C | A | 1 | a0006 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.738C>A | p.His246Gln | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 953/2539 | 738/1362 | 246/453 | chr4 | 8291399 | |||
| chr4:8291466 | G | A | 1 | a0003 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.805G>A | p.Val269Met | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1020/2539 | 805/1362 | 269/453 | chr4 | 8291466 | |||
| chr4:8291473 | C | T | 1 | a0007 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.812C>T | p.Thr271Met | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1027/2539 | 812/1362 | 271/453 | chr4 | 8291473 | |||
| chr4:8291529 | G | A | 1 | a0004 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.868G>A | p.Asp290Asn | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/9 | 1083/2539 | 868/1362 | 290/453 | chr4 | 8291529 | |||
| chr4:8292333 | G | A | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.916G>A | p.Gly306Arg | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/9 | 1131/2539 | 916/1362 | 306/453 | chr4 | 8292333 | |||
| chr4:8304261 | C | T | 1 | a0008 | 1 | NA18999.hp2 | missense_variant | MODERATE | c.1178C>T | p.Pro393Leu | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/9 | 1393/2539 | 1178/1362 | 393/453 | chr4 | 8304261 | |||
| chr4:8306086 | C | T | 1 | a0009 | 1 | NA19067.hp2 | missense_variant | MODERATE | c.1312C>T | p.Arg438Trp | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 1527/2539 | 1312/1362 | 438/453 | chr4 | 8306086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:8270289 | C | T | 1 | a0001c0014 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.321C>T | p.Ser107Ser | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 536/2539 | 321/1362 | 107/453 | chr4 | 8270289 | |||
| chr4:8270316 | G | A | 1 | a0001c0005 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.348G>A | p.Thr116Thr | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 563/2539 | 348/1362 | 116/453 | chr4 | 8270316 | |||
| chr4:8306049 | C | T | 1 | a0001c0011 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1275C>T | p.Ala425Ala | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 1490/2539 | 1275/1362 | 425/453 | chr4 | 8306049 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:8269762 | G | A | 2 | a0001c0001t0004 a0001c0001t0007 |
3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-207G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/9 | 207 | chr4 | 8269762 | ||||||
| chr4:8306200 | A | G | 1 | a0001c0001t0019 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 64 | chr4 | 8306200 | ||||||
| chr4:8306217 | C | T | 1 | a0001c0001t0018 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 81 | chr4 | 8306217 | ||||||
| chr4:8306225 | G | A | 1 | a0001c0001t0008 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 89 | chr4 | 8306225 | ||||||
| chr4:8306273 | A | G | 2 | a0001c0001t0003 a0001c0001t0007 |
4 | HG01109.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 137 | chr4 | 8306273 | ||||||
| chr4:8306325 | C | T | 1 | a0001c0001t0006 | 2 | NA18967.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*189C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 189 | chr4 | 8306325 | ||||||
| chr4:8306331 | G | A | 1 | a0002c0002t0009 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 195 | chr4 | 8306331 | ||||||
| chr4:8306355 | T | C | 1 | a0001c0001t0010 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 219 | chr4 | 8306355 | ||||||
| chr4:8306398 | G | A | 1 | a0001c0001t0011 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 262 | chr4 | 8306398 | ||||||
| chr4:8306449 | C | T | 1 | a0001c0001t0017 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 313 | chr4 | 8306449 | ||||||
| chr4:8306535 | C | A | 1 | a0001c0001t0012 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*399C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 399 | chr4 | 8306535 | ||||||
| chr4:8306561 | G | C | 1 | a0001c0001t0013 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 425 | chr4 | 8306561 | ||||||
| chr4:8306668 | C | G | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(5): Show |
40 | HG00423.hp1 HG01109.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*532C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 532 | chr4 | 8306668 | ||||||
| chr4:8306669 | G | A | 1 | a0001c0001t0014 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 533 | chr4 | 8306669 | ||||||
| chr4:8306719 | C | T | 1 | a0001c0001t0016 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 583 | chr4 | 8306719 | ||||||
| chr4:8306773 | C | T | 1 | a0001c0001t0002 | 3 | HG02886.hp2 HG03486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*637C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 637 | chr4 | 8306773 | ||||||
| chr4:8306784 | C | T | 1 | a0001c0001t0010 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 648 | chr4 | 8306784 | ||||||
| chr4:8306946 | G | T | 1 | a0001c0001t0015 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 810 | chr4 | 8306946 | ||||||
| chr4:8306976 | C | T | 1 | a0001c0001t0005 | 2 | HG02738.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*840C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 9/9 | 840 | chr4 | 8306976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:8270450 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
4 | HG00741.hp1 HG02109.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+97G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270450 | |||||||
| chr4:8270459 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02559.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+106G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270459 | |||||||
| chr4:8270594 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.385+241C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270594 | |||||||
| chr4:8270671 | G | C | 2 | a0001c0001t0002g0038 a0001c0001t0010g0037 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.385+318G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270671 | |||||||
| chr4:8270712 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.385+359T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270712 | |||||||
| chr4:8270935 | C | T | 1 | a0001c0001t0001g0355 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.385+582C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270935 | |||||||
| chr4:8270954 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.385+601C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8270954 | |||||||
| chr4:8271025 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.385+672C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271025 | |||||||
| chr4:8271063 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385+710C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271063 | |||||||
| chr4:8271100 | G | C | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+747G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271100 | |||||||
| chr4:8271193 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385+840C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271193 | |||||||
| chr4:8271227 | AT | A | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.385+880delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8271227 | ||||||
| chr4:8271240 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.385+887T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271240 | |||||||
| chr4:8271243 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
5 | HG01109.hp1 NA18947.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+890G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271243 | |||||||
| chr4:8271295 | C | T | 1 | a0001c0001t0017g0352 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.385+942C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271295 | |||||||
| chr4:8271296 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0045 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.385+943G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271296 | |||||||
| chr4:8271368 | T | C | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+1015T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271368 | |||||||
| chr4:8271520 | C | G | 3 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0001t0001g0351 |
3 | NA18959.hp2 NA18972.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.385+1167C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271520 | |||||||
| chr4:8271637 | C | T | 2 | a0001c0001t0001g0347 a0001c0001t0001g0348 |
2 | NA18944.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.385+1284C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271637 | |||||||
| chr4:8271638 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0341 a0001c0001t0001g0342 others(4): Show |
8 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+1285C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271638 | |||||||
| chr4:8271684 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.385+1331G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271684 | |||||||
| chr4:8271743 | TG | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+1391delG | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271743 | |||||||
| chr4:8271752 | C | G | 1 | a0001c0001t0001g0340 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.385+1399C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271752 | |||||||
| chr4:8271989 | A | G | 1 | a0001c0001t0004g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.385+1636A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8271989 | |||||||
| chr4:8272015 | A | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1662A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272015 | |||||||
| chr4:8272100 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1747C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272100 | |||||||
| chr4:8272225 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+1872C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272225 | |||||||
| chr4:8272351 | C | G | 3 | a0001c0001t0004g0178 a0001c0001t0004g0188 a0001c0001t0007g0177 |
3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+1998C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272351 | |||||||
| chr4:8272402 | G | A | 3 | a0001c0001t0004g0178 a0001c0001t0004g0188 a0001c0001t0007g0177 |
3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+2049G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272402 | |||||||
| chr4:8272403 | TGG | T | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.385+2055_385+2056d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8272403 | ||||||
| chr4:8272404 | G | T | 1 | a0001c0001t0001g0255 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.385+2051G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272404 | |||||||
| chr4:8272435 | G | C | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.385+2082G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272435 | |||||||
| chr4:8272435 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.385+2082G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272435 | |||||||
| chr4:8272491 | C | T | 3 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0009c0010t0001g0277 |
3 | NA18942.hp2 NA18998.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.385+2138C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272491 | |||||||
| chr4:8272521 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.385+2168G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272521 | |||||||
| chr4:8272607 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
25 | HG00733.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.385+2254T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272607 | |||||||
| chr4:8272642 | C | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0173 others(3): Show |
8 | HG02280.hp2 HG02922.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+2289C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272642 | |||||||
| chr4:8272702 | A | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.385+2349A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272702 | |||||||
| chr4:8272773 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+2420C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272773 | |||||||
| chr4:8272841 | C | G | 3 | a0001c0001t0004g0178 a0001c0001t0004g0188 a0001c0001t0007g0177 |
3 | HG02630.hp2 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385+2488C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272841 | |||||||
| chr4:8272881 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.385+2528G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272881 | |||||||
| chr4:8272899 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0354 |
2 | HG01433.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.385+2546G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8272899 | |||||||
| chr4:8273167 | C | A | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.385+2814C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273167 | |||||||
| chr4:8273180 | G | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.385+2827G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273180 | |||||||
| chr4:8273233 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG01168.hp2 HG01257.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.385+2880G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273233 | |||||||
| chr4:8273373 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.385+3020G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273373 | |||||||
| chr4:8273377 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.385+3024A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273377 | |||||||
| chr4:8273456 | T | C | 1 | a0001c0011t0001g0050 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.385+3103T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273456 | |||||||
| chr4:8273522 | TC | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+3176delC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8273522 | ||||||
| chr4:8273528 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385+3175C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273528 | |||||||
| chr4:8273534 | C | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.385+3181C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273534 | |||||||
| chr4:8273534 | C | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.385+3181C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273534 | |||||||
| chr4:8273537 | C | T | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.385+3184C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273537 | |||||||
| chr4:8273588 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(14): Show |
18 | HG00733.hp2 HG01109.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.385+3235G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273588 | |||||||
| chr4:8273652 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.385+3299G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273652 | |||||||
| chr4:8273888 | C | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.385+3535C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273888 | |||||||
| chr4:8273894 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.385+3541T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273894 | |||||||
| chr4:8273902 | T | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.385+3549T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273902 | |||||||
| chr4:8273909 | C | CCCCTCCA others(44): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+3568_385+3569i others(53): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8273909 | ||||||
| chr4:8273909 | C | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.385+3556C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8273909 | |||||||
| chr4:8274060 | G | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.385+3707G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274060 | |||||||
| chr4:8274083 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.385+3730C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274083 | |||||||
| chr4:8274090 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.385+3737G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274090 | |||||||
| chr4:8274380 | G | C | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+4027G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274380 | |||||||
| chr4:8274426 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+4073T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274426 | |||||||
| chr4:8274431 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0158 others(3): Show |
8 | HG01433.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4078G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274431 | |||||||
| chr4:8274454 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(4): Show |
7 | HG01243.hp1 HG01261.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.385+4101C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274454 | |||||||
| chr4:8274465 | C | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.385+4112C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274465 | |||||||
| chr4:8274546 | C | T | 6 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(3): Show |
6 | NA18952.hp2 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+4193C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274546 | |||||||
| chr4:8274612 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.385+4259C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274612 | |||||||
| chr4:8274622 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.385+4269C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274622 | |||||||
| chr4:8274666 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.385+4313T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274666 | |||||||
| chr4:8274684 | A | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.385+4331A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274684 | |||||||
| chr4:8274698 | T | A | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385+4345T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274698 | |||||||
| chr4:8274765 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.385+4412A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274765 | |||||||
| chr4:8274811 | C | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0004g0178 others(2): Show |
5 | HG02602.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+4458C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274811 | |||||||
| chr4:8274812 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.385+4459G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274812 | |||||||
| chr4:8274906 | G | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0004g0178 others(2): Show |
5 | HG02602.hp1 HG02630.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+4553G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274906 | |||||||
| chr4:8274916 | A | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(5): Show |
8 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4563A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274916 | |||||||
| chr4:8274932 | T | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0200 a0001c0001t0001g0201 others(3): Show |
7 | HG02015.hp1 HG02027.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+4579T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274932 | |||||||
| chr4:8274978 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.385+4625T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8274978 | |||||||
| chr4:8275019 | C | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0045 others(63): Show |
69 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.385+4666C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275019 | |||||||
| chr4:8275081 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.385+4728G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275081 | |||||||
| chr4:8275088 | G | C | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG00733.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+4735G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275088 | |||||||
| chr4:8275104 | C | T | 2 | a0001c0001t0001g0150 a0001c0005t0001g0157 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.385+4751C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275104 | |||||||
| chr4:8275184 | C | T | 63 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
68 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.385+4831C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275184 | |||||||
| chr4:8275245 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+4892C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275245 | |||||||
| chr4:8275374 | T | G | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385+5021T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275374 | |||||||
| chr4:8275415 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.385+5062A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275415 | |||||||
| chr4:8275633 | G | T | 2 | a0001c0001t0002g0038 a0001c0001t0010g0037 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.385+5280G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275633 | |||||||
| chr4:8275833 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.385+5480C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275833 | |||||||
| chr4:8275905 | T | C | 6 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(3): Show |
6 | NA18952.hp2 NA18959.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.385+5552T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8275905 | |||||||
| chr4:8276011 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.385+5658C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276011 | |||||||
| chr4:8276033 | G | A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG01243.hp2 HG01928.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+5680G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276033 | |||||||
| chr4:8276108 | G | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(21): Show |
28 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.385+5755G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276108 | |||||||
| chr4:8276296 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.385+5943C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276296 | |||||||
| chr4:8276398 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.386-6039G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276398 | |||||||
| chr4:8276441 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.386-5996C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276441 | |||||||
| chr4:8276494 | G | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(19): Show |
26 | HG01081.hp1 HG01433.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.386-5943G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276494 | |||||||
| chr4:8276666 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.386-5771C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276666 | |||||||
| chr4:8276706 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG00733.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-5731G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276706 | |||||||
| chr4:8276737 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.386-5700G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276737 | |||||||
| chr4:8276813 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.386-5624G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276813 | |||||||
| chr4:8276815 | A | AGCAG | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0002g0038 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-5620_386-5617d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8276815 | ||||||
| chr4:8276826 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-5611C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276826 | |||||||
| chr4:8276844 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-5593C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276844 | |||||||
| chr4:8276876 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.386-5561G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276876 | |||||||
| chr4:8276908 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-5529A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276908 | |||||||
| chr4:8276989 | C | T | 11 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(8): Show |
11 | HG02056.hp2 HG02080.hp1 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-5448C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8276989 | |||||||
| chr4:8277013 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5424C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277013 | |||||||
| chr4:8277077 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.386-5360C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277077 | |||||||
| chr4:8277141 | G | A | 1 | a0001c0001t0017g0352 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.386-5296G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277141 | |||||||
| chr4:8277199 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.386-5238C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277199 | |||||||
| chr4:8277200 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-5237G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277200 | |||||||
| chr4:8277206 | G | T | 1 | a0001c0001t0001g0272 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.386-5231G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277206 | |||||||
| chr4:8277241 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.386-5196G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277241 | |||||||
| chr4:8277306 | G | C | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG00438.hp1 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.386-5131G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277306 | |||||||
| chr4:8277345 | C | A | 1 | a0001c0001t0004g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.386-5092C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277345 | |||||||
| chr4:8277462 | G | A | 2 | a0001c0001t0004g0178 a0001c0001t0007g0177 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.386-4975G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277462 | |||||||
| chr4:8277463 | CT | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.386-4971delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8277463 | ||||||
| chr4:8277466 | T | G | 1 | a0001c0001t0001g0287 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4971T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277466 | |||||||
| chr4:8277469 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4968G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277469 | |||||||
| chr4:8277471 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.386-4966A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277471 | |||||||
| chr4:8277650 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.386-4787G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277650 | |||||||
| chr4:8277692 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.386-4745G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277692 | |||||||
| chr4:8277776 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.386-4661G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277776 | |||||||
| chr4:8277782 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.386-4655C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277782 | |||||||
| chr4:8277783 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.386-4654G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277783 | |||||||
| chr4:8277829 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0010g0037 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.386-4608T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277829 | |||||||
| chr4:8277860 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
7 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-4577A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277860 | |||||||
| chr4:8277959 | G | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
27 | HG01081.hp1 HG01433.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-4478G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8277959 | |||||||
| chr4:8278298 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG01109.hp1 NA18994.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.386-4139C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278298 | |||||||
| chr4:8278313 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.386-4124C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278313 | |||||||
| chr4:8278339 | G | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(244): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.386-4098G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278339 | |||||||
| chr4:8278390 | G | GA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0090 others(9): Show |
13 | HG00544.hp1 HG00609.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-4031dupA | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8278390 | ||||||
| chr4:8278390 | GA | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.386-4031delA | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8278390 | ||||||
| chr4:8278533 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.386-3904C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278533 | |||||||
| chr4:8278580 | C | G | 5 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | NA18941.hp1 NA18949.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-3857C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278580 | |||||||
| chr4:8278604 | C | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.386-3833C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278604 | |||||||
| chr4:8278630 | G | A | 1 | a0001c0001t0001g0291 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.386-3807G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278630 | |||||||
| chr4:8278660 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.386-3777C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278660 | |||||||
| chr4:8278769 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(195): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.386-3668C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278769 | |||||||
| chr4:8278798 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.386-3639A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278798 | |||||||
| chr4:8278866 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.386-3571G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8278866 | |||||||
| chr4:8279046 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.386-3391T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279046 | |||||||
| chr4:8279273 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02080.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.386-3164C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279273 | |||||||
| chr4:8279419 | C | G | 1 | a0002c0002t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.386-3018C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279419 | |||||||
| chr4:8279438 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.386-2999G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279438 | |||||||
| chr4:8279459 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386-2978C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279459 | |||||||
| chr4:8279490 | G | A | 2 | a0001c0001t0001g0150 a0001c0005t0001g0157 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.386-2947G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279490 | |||||||
| chr4:8279542 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.386-2895C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279542 | |||||||
| chr4:8279673 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.386-2764C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279673 | |||||||
| chr4:8279734 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-2703T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279734 | |||||||
| chr4:8279757 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.386-2680C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279757 | |||||||
| chr4:8279913 | C | G | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.386-2524C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279913 | |||||||
| chr4:8279932 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0290 a0001c0001t0001g0292 others(5): Show |
9 | NA18942.hp1 NA18953.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-2505C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279932 | |||||||
| chr4:8279961 | AC | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02109.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-2475delC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279961 | |||||||
| chr4:8279964 | A | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.386-2473A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279964 | |||||||
| chr4:8279964 | A | T | 2 | a0001c0001t0004g0178 a0001c0001t0007g0177 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.386-2473A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8279964 | |||||||
| chr4:8280099 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.386-2338C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280099 | |||||||
| chr4:8280126 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.386-2311A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280126 | |||||||
| chr4:8280155 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.386-2282C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280155 | |||||||
| chr4:8280274 | G | T | 1 | a0001c0001t0001g0268 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.386-2163G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280274 | |||||||
| chr4:8280333 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02080.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.386-2104G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280333 | |||||||
| chr4:8280377 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.386-2060C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280377 | |||||||
| chr4:8280383 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.386-2054T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280383 | |||||||
| chr4:8280397 | A | C | 1 | a0001c0005t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.386-2040A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280397 | |||||||
| chr4:8280447 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.386-1990C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280447 | |||||||
| chr4:8280483 | C | T | 2 | a0001c0001t0006g0333 a0001c0001t0006g0334 |
2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.386-1954C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280483 | |||||||
| chr4:8280533 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-1904G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280533 | |||||||
| chr4:8280563 | G | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0089 others(3): Show |
6 | HG02572.hp1 HG02965.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-1874G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280563 | |||||||
| chr4:8280580 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.386-1857C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280580 | |||||||
| chr4:8280615 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.386-1822T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280615 | |||||||
| chr4:8280712 | G | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG02145.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1725G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280712 | |||||||
| chr4:8280731 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.386-1706G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280731 | |||||||
| chr4:8280735 | G | GC | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.386-1700dupC | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 8280735 | ||||||
| chr4:8280738 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-1699G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280738 | |||||||
| chr4:8280740 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.386-1697C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280740 | |||||||
| chr4:8280835 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1602C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280835 | |||||||
| chr4:8280896 | T | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.386-1541T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280896 | |||||||
| chr4:8280976 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | NA18952.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.386-1461G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8280976 | |||||||
| chr4:8281044 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG00733.hp2 HG01109.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.386-1393C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281044 | |||||||
| chr4:8281084 | A | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1353A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281084 | |||||||
| chr4:8281150 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-1287G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281150 | |||||||
| chr4:8281182 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.386-1255C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281182 | |||||||
| chr4:8281265 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.386-1172C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281265 | |||||||
| chr4:8281393 | C | G | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1044C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281393 | |||||||
| chr4:8281396 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0014g0207 |
3 | HG00642.hp1 HG02109.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.386-1041G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281396 | |||||||
| chr4:8281451 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.386-986G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281451 | |||||||
| chr4:8281518 | A | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.386-919A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281518 | |||||||
| chr4:8281531 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-906A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281531 | |||||||
| chr4:8281595 | G | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.386-842G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281595 | |||||||
| chr4:8281601 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386-836G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281601 | |||||||
| chr4:8281660 | C | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.386-777C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281660 | |||||||
| chr4:8281695 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.386-742G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281695 | |||||||
| chr4:8281748 | T | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.386-689T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281748 | |||||||
| chr4:8281766 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-671G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281766 | |||||||
| chr4:8281767 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.386-670A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281767 | |||||||
| chr4:8281784 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.386-653G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281784 | |||||||
| chr4:8281806 | A | G | 2 | a0001c0001t0001g0353 a0001c0001t0003g0183 |
2 | HG01109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.386-631A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281806 | |||||||
| chr4:8281903 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.386-534C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8281903 | |||||||
| chr4:8282021 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0003g0183 |
2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.386-416G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282021 | |||||||
| chr4:8282021 | G | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(147): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.386-416G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282021 | |||||||
| chr4:8282110 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.386-327T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282110 | |||||||
| chr4:8282114 | G | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
8 | HG02257.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-323G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282114 | |||||||
| chr4:8282293 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.386-144G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282293 | |||||||
| chr4:8282357 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.386-80T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282357 | |||||||
| chr4:8282397 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.386-40G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 1/8 | chr4 | 8282397 | |||||||
| chr4:8282600 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.485+64G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282600 | |||||||
| chr4:8282652 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.485+116C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282652 | |||||||
| chr4:8282817 | A | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0342 a0001c0001t0011g0343 others(2): Show |
6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+281A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282817 | |||||||
| chr4:8282846 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.485+310G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282846 | |||||||
| chr4:8282948 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0301 |
2 | HG01168.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.485+412G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8282948 | |||||||
| chr4:8283008 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485+472G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283008 | |||||||
| chr4:8283236 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485+700G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283236 | |||||||
| chr4:8283462 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.485+926G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283462 | |||||||
| chr4:8283466 | T | C | 1 | a0001c0001t0010g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485+930T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283466 | |||||||
| chr4:8283603 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.485+1067G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283603 | |||||||
| chr4:8283652 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.485+1116G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283652 | |||||||
| chr4:8283665 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
9 | HG00558.hp2 HG02004.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.485+1129A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283665 | |||||||
| chr4:8283692 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.485+1156G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283692 | |||||||
| chr4:8283713 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0353 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.485+1177C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283713 | |||||||
| chr4:8283773 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.485+1237G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283773 | |||||||
| chr4:8283807 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.485+1271C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283807 | |||||||
| chr4:8283868 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.485+1332T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283868 | |||||||
| chr4:8283892 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0286 |
2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.485+1356C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283892 | |||||||
| chr4:8283919 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02698.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.485+1383G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283919 | |||||||
| chr4:8283967 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.485+1431C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283967 | |||||||
| chr4:8283969 | C | T | 1 | a0001c0005t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.485+1433C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283969 | |||||||
| chr4:8283996 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.485+1460C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8283996 | |||||||
| chr4:8284091 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0004g0178 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.485+1555G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284091 | |||||||
| chr4:8284170 | C | T | 1 | a0002c0002t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.485+1634C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284170 | |||||||
| chr4:8284179 | G | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
28 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.485+1643G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284179 | |||||||
| chr4:8284246 | C | T | 1 | a0001c0001t0008g0324 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.485+1710C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284246 | |||||||
| chr4:8284276 | A | G | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.485+1740A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284276 | |||||||
| chr4:8284361 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.485+1825A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284361 | |||||||
| chr4:8284395 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.485+1859G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284395 | |||||||
| chr4:8284547 | G | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+2011G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284547 | |||||||
| chr4:8284575 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
25 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.486-1986C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284575 | |||||||
| chr4:8284615 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.486-1946C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284615 | |||||||
| chr4:8284683 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.486-1878G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284683 | |||||||
| chr4:8284899 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.486-1662G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8284899 | |||||||
| chr4:8285052 | G | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-1509G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285052 | |||||||
| chr4:8285071 | G | C | 1 | a0001c0001t0007g0177 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.486-1490G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285071 | |||||||
| chr4:8285115 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.486-1446C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285115 | |||||||
| chr4:8285189 | G | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.486-1372G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285189 | |||||||
| chr4:8285311 | T | A | 1 | a0001c0005t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.486-1250T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285311 | |||||||
| chr4:8285470 | C | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-1091C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285470 | |||||||
| chr4:8285625 | G | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.486-936G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285625 | |||||||
| chr4:8285725 | C | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-836C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285725 | |||||||
| chr4:8285734 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.486-827C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285734 | |||||||
| chr4:8285760 | A | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-801A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285760 | |||||||
| chr4:8285767 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.486-794A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285767 | |||||||
| chr4:8285836 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.486-725G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285836 | |||||||
| chr4:8285940 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0158 |
3 | HG02145.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.486-621C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285940 | |||||||
| chr4:8285959 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0169 a0001c0001t0002g0038 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-602G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8285959 | |||||||
| chr4:8286015 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.486-546C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286015 | |||||||
| chr4:8286056 | T | G | 126 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(123): Show |
138 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.486-505T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286056 | |||||||
| chr4:8286088 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.486-473C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286088 | |||||||
| chr4:8286115 | G | A | 1 | a0001c0001t0001g0330 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.486-446G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286115 | |||||||
| chr4:8286142 | C | G | 1 | a0005c0009t0001g0345 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.486-419C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286142 | |||||||
| chr4:8286206 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.486-355G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286206 | |||||||
| chr4:8286264 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.486-297G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286264 | |||||||
| chr4:8286301 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.486-260G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286301 | |||||||
| chr4:8286381 | C | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0353 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.486-180C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286381 | |||||||
| chr4:8286499 | C | G | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.486-62C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 2/8 | chr4 | 8286499 | |||||||
| chr4:8286794 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.708+11G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286794 | |||||||
| chr4:8286807 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0005g0122 |
2 | HG02965.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.708+24C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286807 | |||||||
| chr4:8286854 | A | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.708+71A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286854 | |||||||
| chr4:8286885 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.708+102A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286885 | |||||||
| chr4:8286943 | T | C | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.708+160T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286943 | |||||||
| chr4:8286980 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.708+197T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286980 | |||||||
| chr4:8286986 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.708+203G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8286986 | |||||||
| chr4:8287094 | G | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0185 a0001c0001t0001g0195 |
3 | HG01261.hp2 HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.708+311G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287094 | |||||||
| chr4:8287188 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.708+405A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287188 | |||||||
| chr4:8287231 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG00642.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.708+448C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287231 | |||||||
| chr4:8287270 | C | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.708+487C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287270 | |||||||
| chr4:8287428 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.708+645A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287428 | |||||||
| chr4:8287480 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.708+697G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287480 | |||||||
| chr4:8287526 | G | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(256): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.708+743G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287526 | |||||||
| chr4:8287529 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.708+746A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287529 | |||||||
| chr4:8287561 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.708+778G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287561 | |||||||
| chr4:8287595 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0003g0183 |
2 | HG01109.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.708+812C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287595 | |||||||
| chr4:8287626 | C | G | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.708+843C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287626 | |||||||
| chr4:8287685 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.708+902C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287685 | |||||||
| chr4:8287707 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.708+924A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287707 | |||||||
| chr4:8287713 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.708+930T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287713 | |||||||
| chr4:8287722 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0001g0169 a0001c0001t0002g0038 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.708+939C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287722 | |||||||
| chr4:8287772 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.708+989C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287772 | |||||||
| chr4:8287784 | G | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0284 a0001c0001t0001g0286 others(1): Show |
4 | HG00438.hp1 HG02165.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+1001G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287784 | |||||||
| chr4:8287816 | C | T | 2 | a0001c0001t0001g0075 a0001c0011t0001g0050 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.708+1033C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287816 | |||||||
| chr4:8287819 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0353 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.708+1036C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287819 | |||||||
| chr4:8287909 | T | G | 2 | a0001c0001t0003g0346 a0001c0001t0007g0177 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.708+1126T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287909 | |||||||
| chr4:8287990 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1207G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287990 | |||||||
| chr4:8287991 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1208A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8287991 | |||||||
| chr4:8288080 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.708+1297A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288080 | |||||||
| chr4:8288082 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.708+1299C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288082 | |||||||
| chr4:8288170 | T | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.708+1387T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288170 | |||||||
| chr4:8288177 | A | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.708+1394A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288177 | |||||||
| chr4:8288188 | T | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0085 others(2): Show |
7 | HG01070.hp2 HG01168.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+1405T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288188 | |||||||
| chr4:8288190 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.708+1407G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288190 | |||||||
| chr4:8288231 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.708+1448G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288231 | |||||||
| chr4:8288261 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.708+1478G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288261 | |||||||
| chr4:8288310 | G | T | 1 | a0001c0001t0001g0329 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.708+1527G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288310 | |||||||
| chr4:8288313 | G | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
25 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.708+1530G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288313 | |||||||
| chr4:8288329 | A | C | 1 | a0001c0001t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.708+1546A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288329 | |||||||
| chr4:8288386 | G | GCCTCAGC others(36): Show |
1 | a0001c0001t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.708+1605_708+1647d others(45): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288386 | ||||||
| chr4:8288574 | C | CT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0126 a0001c0001t0001g0168 others(5): Show |
10 | HG00558.hp1 HG01175.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.708+1807dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | ||||||
| chr4:8288574 | CT | C | 7 | a0001c0001t0001g0053 a0001c0001t0001g0074 a0001c0001t0001g0141 others(4): Show |
7 | HG01167.hp2 HG01934.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+1807delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | ||||||
| chr4:8288574 | CTT | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.708+1806_708+1807d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | ||||||
| chr4:8288574 | CTTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(8): Show |
12 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.708+1805_708+1807d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288574 | ||||||
| chr4:8288614 | C | T | 2 | a0001c0001t0010g0037 a0001c0001t0015g0133 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.708+1831C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288614 | |||||||
| chr4:8288707 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+1924T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288707 | |||||||
| chr4:8288853 | G | A | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | NA18962.hp2 NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.708+2070G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288853 | |||||||
| chr4:8288864 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.708+2081C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288864 | |||||||
| chr4:8288878 | T | TTTCC | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(24): Show |
29 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.708+2108_708+2111d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288878 | T | TTTCCTTC others(1): Show |
34 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0029 others(31): Show |
37 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.708+2104_708+2111d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288878 | T | TTTCCTTC others(5): Show |
31 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0057 others(28): Show |
32 | HG00544.hp1 HG01433.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.708+2100_708+2111d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288878 | T | TTTCCTTC others(9): Show |
24 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0062 others(21): Show |
24 | HG00323.hp1 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+2096_708+2111d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288878 | T | TTTCCTTC others(13): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG01074.hp2 HG02055.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.708+2111_708+2112i others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288878 | T | TTTCCTTC others(17): Show |
1 | a0001c0001t0001g0007 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.708+2111_708+2112i others(26): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288878 | ||||||
| chr4:8288883 | TTCCTTCC others(9): Show |
T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0264 |
2 | HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.708+2112_708+2127d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288883 | ||||||
| chr4:8288887 | TTCCTTCC others(5): Show |
T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
16 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+2112_708+2123d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288887 | ||||||
| chr4:8288891 | TTCCG | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(76): Show |
86 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.708+2116_708+2119d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288891 | ||||||
| chr4:8288891 | TTCCGTCC others(1): Show |
T | 24 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0023 others(21): Show |
26 | HG00408.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.708+2112_708+2119d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288891 | ||||||
| chr4:8288895 | G | T | 144 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(141): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.708+2112G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288895 | |||||||
| chr4:8288899 | G | GTCCT | 5 | a0001c0001t0001g0162 a0001c0001t0001g0292 a0001c0001t0001g0306 others(2): Show |
5 | HG00423.hp2 HG02647.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+2149_708+2152d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | ||||||
| chr4:8288899 | G | GTCCTTCC others(1): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0089 others(4): Show |
8 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.708+2145_708+2152d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | ||||||
| chr4:8288899 | G | GTCCTTCC others(5): Show |
3 | a0001c0001t0001g0034 a0001c0001t0001g0184 a0001c0001t0001g0186 |
3 | HG02257.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.708+2141_708+2152d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | ||||||
| chr4:8288899 | G | GTCCTTCC others(9): Show |
2 | a0001c0001t0002g0038 a0001c0001t0004g0188 |
2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.708+2137_708+2152d others(18): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | ||||||
| chr4:8288899 | G | GTCCTTCC others(13): Show |
2 | a0001c0001t0001g0150 a0001c0001t0004g0178 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.708+2133_708+2152d others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8288899 | ||||||
| chr4:8288899 | G | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(219): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.708+2116G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288899 | |||||||
| chr4:8288932 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.708+2149T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288932 | |||||||
| chr4:8288935 | T | TTCCTTCC others(3): Show |
1 | a0001c0001t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.708+2152_708+2153i others(12): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288935 | |||||||
| chr4:8288936 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
5 | NA18947.hp1 NA18948.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.708+2153C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288936 | |||||||
| chr4:8288937 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.708+2154C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288937 | |||||||
| chr4:8288945 | C | T | 2 | a0001c0001t0010g0037 a0001c0001t0015g0133 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.708+2162C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288945 | |||||||
| chr4:8288949 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.708+2166T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288949 | |||||||
| chr4:8288951 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.708+2168T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288951 | |||||||
| chr4:8288981 | G | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.708+2198G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8288981 | |||||||
| chr4:8289031 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.708+2248C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289031 | |||||||
| chr4:8289037 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.708+2254A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289037 | |||||||
| chr4:8289056 | C | T | 1 | a0001c0001t0001g0348 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.708+2273C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289056 | |||||||
| chr4:8289176 | G | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
228 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.709-2194G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289176 | |||||||
| chr4:8289268 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.709-2102C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289268 | |||||||
| chr4:8289348 | C | G | 1 | a0002c0002t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.709-2022C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289348 | |||||||
| chr4:8289358 | A | T | 1 | a0001c0005t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.709-2012A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289358 | |||||||
| chr4:8289375 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(168): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.709-1995C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289375 | |||||||
| chr4:8289458 | C | T | 5 | a0001c0001t0001g0196 a0001c0001t0001g0353 a0001c0001t0003g0183 others(2): Show |
5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-1912C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289458 | |||||||
| chr4:8289460 | T | C | 5 | a0001c0001t0001g0196 a0001c0001t0001g0353 a0001c0001t0003g0183 others(2): Show |
5 | HG01109.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.709-1910T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289460 | |||||||
| chr4:8289652 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0072 |
3 | HG02056.hp1 NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.709-1718C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289652 | |||||||
| chr4:8289707 | G | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.709-1663G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289707 | |||||||
| chr4:8289794 | A | ACCCTCCT others(112): Show |
21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-1551_709-1433d others(121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8289794 | ||||||
| chr4:8289898 | TGGCCTCA others(53): Show |
T | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.709-1457_709-1398d others(62): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 8289898 | ||||||
| chr4:8289954 | T | C | 6 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG00423.hp2 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-1416T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289954 | |||||||
| chr4:8289958 | C | T | 6 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
6 | HG00423.hp2 HG02074.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-1412C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289958 | |||||||
| chr4:8289973 | A | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
23 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.709-1397A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289973 | |||||||
| chr4:8289996 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0004g0178 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.709-1374C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8289996 | |||||||
| chr4:8290039 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
17 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.709-1331C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290039 | |||||||
| chr4:8290060 | C | T | 32 | a0001c0001t0001g0041 a0001c0001t0001g0045 a0001c0001t0001g0060 others(29): Show |
34 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.709-1310C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290060 | |||||||
| chr4:8290061 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0347 |
2 | HG02965.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.709-1309G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290061 | |||||||
| chr4:8290124 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.709-1246C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290124 | |||||||
| chr4:8290176 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.709-1194G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290176 | |||||||
| chr4:8290183 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.709-1187G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290183 | |||||||
| chr4:8290191 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.709-1179T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290191 | |||||||
| chr4:8290254 | T | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(74): Show |
83 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.709-1116T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290254 | |||||||
| chr4:8290352 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.709-1018C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290352 | |||||||
| chr4:8290466 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
7 | HG01433.hp2 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.709-904G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290466 | |||||||
| chr4:8290475 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0034 others(10): Show |
15 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.709-895C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290475 | |||||||
| chr4:8290513 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
6 | HG01433.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-857C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290513 | |||||||
| chr4:8290534 | C | T | 1 | a0001c0001t0004g0188 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.709-836C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290534 | |||||||
| chr4:8290637 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.709-733C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290637 | |||||||
| chr4:8290819 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
17 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.709-551G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290819 | |||||||
| chr4:8290830 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(275): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.709-540T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290830 | |||||||
| chr4:8290875 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(15): Show |
19 | HG01243.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.709-495G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290875 | |||||||
| chr4:8290886 | C | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0015 others(120): Show |
136 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.709-484C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290886 | |||||||
| chr4:8290906 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.709-464G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290906 | |||||||
| chr4:8290950 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-420A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290950 | |||||||
| chr4:8290974 | A | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(18): Show |
24 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-396A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8290974 | |||||||
| chr4:8291100 | A | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.709-270A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291100 | |||||||
| chr4:8291150 | A | G | 1 | a0001c0001t0015g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.709-220A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291150 | |||||||
| chr4:8291263 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.709-107G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291263 | |||||||
| chr4:8291315 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.709-55G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291315 | |||||||
| chr4:8291321 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
6 | HG01433.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-49G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 3/8 | chr4 | 8291321 | |||||||
| chr4:8291629 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.903+65G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291629 | |||||||
| chr4:8291652 | C | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.903+88C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291652 | |||||||
| chr4:8291653 | T | C | 49 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(46): Show |
51 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.903+89T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291653 | |||||||
| chr4:8291671 | C | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.903+107C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291671 | |||||||
| chr4:8291675 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.903+111C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291675 | |||||||
| chr4:8291691 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.903+127T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291691 | |||||||
| chr4:8291716 | T | C | 43 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(40): Show |
45 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.903+152T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291716 | |||||||
| chr4:8291829 | C | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(329): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.903+265C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291829 | |||||||
| chr4:8291866 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG01243.hp1 HG02572.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+302T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291866 | |||||||
| chr4:8291956 | C | G | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.904-365C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8291956 | |||||||
| chr4:8292004 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.904-317G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292004 | |||||||
| chr4:8292008 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0342 a0001c0001t0011g0343 others(2): Show |
6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-313C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292008 | |||||||
| chr4:8292063 | CTGCCTGG others(15): Show |
C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0126 |
2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.904-253_904-232del others(22): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 8292063 | ||||||
| chr4:8292072 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904-249C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292072 | |||||||
| chr4:8292075 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.904-246C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292075 | |||||||
| chr4:8292247 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.904-74C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 4/8 | chr4 | 8292247 | |||||||
| chr4:8292443 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+90A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292443 | |||||||
| chr4:8292469 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(96): Show |
106 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.936+116C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292469 | |||||||
| chr4:8292524 | C | T | 1 | a0001c0001t0001g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.936+171C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292524 | |||||||
| chr4:8292567 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.936+214C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292567 | |||||||
| chr4:8292602 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG00558.hp2 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+249C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292602 | |||||||
| chr4:8292612 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.936+259G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292612 | |||||||
| chr4:8292688 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.936+335C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292688 | |||||||
| chr4:8292822 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
102 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.936+469C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292822 | |||||||
| chr4:8292823 | G | A | 18 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): Show |
18 | HG02080.hp1 HG02109.hp2 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.936+470G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292823 | |||||||
| chr4:8292824 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.936+471G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8292824 | |||||||
| chr4:8293020 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.936+667C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293020 | |||||||
| chr4:8293152 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.936+799C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293152 | |||||||
| chr4:8293283 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.937-804G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293283 | |||||||
| chr4:8293293 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.937-794C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293293 | |||||||
| chr4:8293330 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.937-757G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293330 | |||||||
| chr4:8293403 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.937-684C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293403 | |||||||
| chr4:8293559 | T | A | 1 | a0004c0008t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.937-528T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293559 | |||||||
| chr4:8293607 | G | A | 1 | a0001c0001t0001g0017 | 2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.937-480G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293607 | |||||||
| chr4:8293696 | G | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0002g0038 others(1): Show |
4 | HG00741.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.937-391G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293696 | |||||||
| chr4:8293844 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.937-243G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293844 | |||||||
| chr4:8293878 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.937-209A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8293878 | |||||||
| chr4:8294054 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0124 a0001c0001t0001g0131 others(7): Show |
11 | HG02258.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.937-33C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 5/8 | chr4 | 8294054 | |||||||
| chr4:8294222 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0152 others(2): Show |
7 | HG01884.hp1 HG02280.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+21G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294222 | |||||||
| chr4:8294415 | G | A | 92 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(89): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1051+214G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294415 | |||||||
| chr4:8294570 | G | A | 3 | a0001c0001t0004g0188 a0001c0001t0010g0037 a0002c0002t0001g0069 |
3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+369G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294570 | |||||||
| chr4:8294574 | G | A | 1 | a0001c0005t0001g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1051+373G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294574 | |||||||
| chr4:8294578 | G | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0051 others(17): Show |
22 | HG00423.hp1 HG01261.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1051+377G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294578 | |||||||
| chr4:8294582 | G | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1051+381G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294582 | |||||||
| chr4:8294612 | C | CCATCCAT others(1108): Show |
1 | a0001c0001t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294612 | ||||||
| chr4:8294614 | A | ACCCACCC others(149): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0181 |
2 | HG00733.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051+413_1051+414i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294614 | |||||||
| chr4:8294614 | A | ACCCACCC others(153): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0131 |
2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1051+413_1051+414i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294614 | |||||||
| chr4:8294614 | A | ATCCACCC others(149): Show |
1 | a0001c0001t0001g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294614 | ||||||
| chr4:8294615 | T | TCCACCCA others(129): Show |
1 | a0001c0001t0001g0168 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1051+417_1051+418i others(138): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | ||||||
| chr4:8294615 | T | TCCACCCA others(133): Show |
9 | a0001c0001t0001g0034 a0001c0001t0001g0089 a0001c0001t0001g0097 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | ||||||
| chr4:8294615 | T | TCCACCCA others(25): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0119 others(6): Show |
11 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(34): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | ||||||
| chr4:8294615 | T | TCCACCCA others(37): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0195 a0001c0001t0001g0258 |
3 | HG01261.hp2 HG01891.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(46): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294615 | ||||||
| chr4:8294616 | C | CCACCCAC others(141): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0154 |
5 | HG02145.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(33): Show |
1 | a0004c0008t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(1053): Show |
1 | a0001c0001t0001g0251 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(1062): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(1096): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(4): Show |
10 | HG01192.hp1 HG01255.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0015g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1051+417_1051+418i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(137): Show |
7 | a0001c0001t0001g0035 a0001c0001t0001g0092 a0001c0001t0001g0121 others(4): Show |
7 | HG01175.hp2 HG02040.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(141): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0026 others(49): Show |
59 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(145): Show |
15 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0041 others(12): Show |
16 | HG02523.hp1 HG02735.hp2 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(137): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0134 others(3): Show |
6 | HG00741.hp1 HG01243.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCACCCAC others(141): Show |
2 | a0001c0001t0002g0038 a0001c0001t0002g0098 |
2 | HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294616 | C | CCATCCAT others(1104): Show |
1 | a0001c0001t0001g0288 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294616 | ||||||
| chr4:8294618 | A | ACCCACCC others(141): Show |
2 | a0001c0001t0001g0164 a0001c0001t0014g0207 |
2 | HG00642.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | |||||||
| chr4:8294618 | A | ACCCACCC others(145): Show |
65 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(62): Show |
71 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | |||||||
| chr4:8294618 | A | ACCCACCC others(149): Show |
26 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0031 others(23): Show |
28 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1051+417_1051+418i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | |||||||
| chr4:8294618 | A | ACCCACCC others(153): Show |
2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1051+417_1051+418i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | |||||||
| chr4:8294618 | A | ACCCACCC others(141): Show |
1 | a0001c0001t0001g0115 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1051+417_1051+418i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294618 | |||||||
| chr4:8294618 | A | ATCCACCC others(145): Show |
1 | a0002c0002t0001g0127 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | ||||||
| chr4:8294618 | A | ATCCACCC others(149): Show |
3 | a0001c0001t0001g0064 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG01884.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | ||||||
| chr4:8294618 | A | ATCCACCC others(153): Show |
1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | ||||||
| chr4:8294618 | A | ATCCATCC others(153): Show |
1 | a0001c0001t0010g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294618 | ||||||
| chr4:8294619 | T | C | 1 | a0004c0008t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+418T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294619 | |||||||
| chr4:8294619 | T | TCCACCCA others(37): Show |
1 | a0001c0001t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(46): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294619 | ||||||
| chr4:8294619 | T | TCCACCCA others(33): Show |
1 | a0001c0001t0001g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294619 | ||||||
| chr4:8294620 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0108 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(33): Show |
5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0159 others(2): Show |
5 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(42): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(133): Show |
1 | a0001c0001t0001g0341 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(1084): Show |
1 | a0001c0001t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1093): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(1096): Show |
27 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0106 others(24): Show |
29 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0003g0161 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1051+421_1051+422i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(1104): Show |
2 | a0001c0001t0003g0346 a0001c0001t0007g0177 |
2 | HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCACCCAC others(141): Show |
1 | a0001c0001t0003g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+421_1051+422i others(150): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCATCCAC others(1100): Show |
16 | a0001c0001t0001g0022 a0001c0001t0001g0156 a0001c0001t0001g0206 others(13): Show |
17 | HG00738.hp2 HG01192.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCATCCAC others(1104): Show |
1 | a0001c0001t0001g0310 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294620 | C | CCATCCAC others(1096): Show |
1 | a0008c0012t0001g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294620 | ||||||
| chr4:8294622 | A | ACCCACCC others(145): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0074 others(1): Show |
6 | HG01167.hp2 HG02280.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+421_1051+422i others(154): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294622 | |||||||
| chr4:8294622 | A | ACCCACCC others(149): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0302 |
2 | HG00609.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1051+421_1051+422i others(158): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294622 | |||||||
| chr4:8294623 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0159 others(2): Show |
5 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051+422T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294623 | |||||||
| chr4:8294624 | C | CCACCCAC others(133): Show |
1 | a0001c0001t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(142): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1096): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0232 |
2 | HG00438.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1096): Show |
43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(40): Show |
47 | HG00408.hp1 HG01071.hp2 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0311 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0143 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1096): Show |
1 | a0001c0001t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1105): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1100): Show |
1 | a0001c0001t0001g0289 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1097): Show |
1 | a0001c0001t0001g0351 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1106): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1092): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0238 |
3 | HG00280.hp2 HG00544.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(1101): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCACCCAC others(1104): Show |
1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1051+425_1051+426i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCATCCAC others(1100): Show |
1 | a0001c0001t0001g0268 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1051+429_1051+430i others(1109): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | CCATCCAT others(1104): Show |
1 | a0001c0001t0001g0261 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1051+433_1051+434i others(1113): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294624 | ||||||
| chr4:8294624 | C | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0034 others(16): Show |
21 | HG00423.hp1 HG01891.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1051+423C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294624 | |||||||
| chr4:8294626 | A | ACCCACCC others(153): Show |
2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+425_1051+426i others(162): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294626 | |||||||
| chr4:8294626 | A | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
89 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.1051+425A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294626 | |||||||
| chr4:8294627 | T | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0119 others(6): Show |
11 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051+426T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294627 | |||||||
| chr4:8294630 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+429A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294630 | |||||||
| chr4:8294631 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1051+430T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294631 | |||||||
| chr4:8294634 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+433A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294634 | |||||||
| chr4:8294659 | T | TCCA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0169 others(8): Show |
15 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1051+459_1051+461d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294659 | ||||||
| chr4:8294659 | T | TCCACCAT others(85): Show |
1 | a0001c0001t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294659 | ||||||
| chr4:8294662 | A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0124 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | |||||||
| chr4:8294662 | A | ACTTATCC others(1008): Show |
5 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG02080.hp1 HG02886.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | |||||||
| chr4:8294662 | A | ACTTATCC others(1012): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0164 |
2 | HG00609.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | |||||||
| chr4:8294662 | A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1051+461_1051+462i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | |||||||
| chr4:8294662 | A | ACTTATCC others(1008): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0154 |
3 | HG02559.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1051+461_1051+462i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294662 | |||||||
| chr4:8294663 | T | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0083 others(8): Show |
13 | HG00609.hp2 HG00733.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1051+462T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294663 | |||||||
| chr4:8294663 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+462T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294663 | |||||||
| chr4:8294663 | T | TCCACCAT others(85): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0140 a0001c0001t0001g0206 others(2): Show |
6 | HG00738.hp2 HG01192.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1008): Show |
1 | a0001c0001t0001g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0131 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1015): Show |
1 | a0001c0001t0013g0114 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1024): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1016): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0063 others(4): Show |
9 | HG00642.hp2 HG01515.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1020): Show |
1 | a0001c0001t0001g0179 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294663 | T | TCCACTTA others(1020): Show |
1 | a0001c0001t0010g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294663 | ||||||
| chr4:8294664 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1051+463C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294664 | |||||||
| chr4:8294666 | A | ACCATCCA others(81): Show |
28 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0076 others(25): Show |
30 | HG00408.hp2 HG00558.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(90): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1049): Show |
1 | a0001c0001t0001g0247 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1058): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1005): Show |
1 | a0001c0001t0001g0330 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1014): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(989): Show |
1 | a0001c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(998): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1004): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0185 |
2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1013): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
1 | a0001c0001t0003g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
12 | a0001c0001t0001g0029 a0001c0001t0001g0090 a0001c0001t0001g0230 others(9): Show |
13 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
1 | a0001c0001t0001g0129 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0107 others(2): Show |
5 | HG00140.hp2 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1012): Show |
37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(34): Show |
40 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1016): Show |
1 | a0001c0001t0001g0062 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1012): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0171 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1012): Show |
1 | a0001c0001t0001g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
1 | a0001c0001t0001g0332 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294666 | A | ACTTATCC others(1008): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0153 |
3 | HG01891.hp1 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1051+465_1051+466i others(1017): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294666 | |||||||
| chr4:8294667 | T | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(94): Show |
104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1051+466T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | |||||||
| chr4:8294667 | T | TACATCTG others(1137): Show |
1 | a0001c0001t0001g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1051+466_1051+467i others(1146): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | |||||||
| chr4:8294667 | T | TACATCTG others(1112): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1051+466_1051+467i others(1121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294667 | |||||||
| chr4:8294667 | T | TCCACCAT others(85): Show |
73 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0023 others(70): Show |
77 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(94): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACCCA others(74): Show |
12 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0169 others(9): Show |
16 | HG00280.hp1 HG00639.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(83): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(993): Show |
1 | a0001c0001t0001g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1002): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1044): Show |
1 | a0001c0001t0001g0236 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1053): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1048): Show |
1 | a0001c0001t0001g0341 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1057): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1012): Show |
66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(63): Show |
73 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1012): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG00741.hp2 HG01167.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1016): Show |
17 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
20 | HG00639.hp2 HG01261.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0074 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1020): Show |
2 | a0001c0001t0001g0196 a0001c0001t0001g0285 |
2 | HG02155.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1029): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1012): Show |
9 | a0001c0001t0001g0028 a0001c0001t0001g0125 a0001c0001t0001g0276 others(6): Show |
10 | NA18942.hp1 NA18953.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1012): Show |
8 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0158 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCCACTTA others(1013): Show |
1 | a0001c0001t0001g0317 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(1022): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294667 | T | TCTGTCCA others(1108): Show |
1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1051+467_1051+468i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294667 | ||||||
| chr4:8294668 | C | A | 1 | a0004c0008t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+467C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294668 | |||||||
| chr4:8294670 | A | ACCATCCA others(81): Show |
1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1051+469_1051+470i others(90): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294670 | |||||||
| chr4:8294670 | A | ACTTATCC others(1012): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0147 a0001c0001t0001g0162 |
3 | HG01074.hp2 HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1051+469_1051+470i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294670 | |||||||
| chr4:8294671 | T | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0147 a0001c0001t0001g0162 others(1): Show |
4 | HG01074.hp2 HG02647.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051+470T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294671 | |||||||
| chr4:8294671 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+470T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294671 | |||||||
| chr4:8294671 | T | TCCACTTA others(1012): Show |
2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+473_1051+474i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | ||||||
| chr4:8294671 | T | TCCACTTA others(1016): Show |
1 | a0001c0001t0001g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1051+473_1051+474i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | ||||||
| chr4:8294671 | T | TCTGTCCA others(1108): Show |
1 | a0004c0008t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1051+471_1051+472i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294671 | ||||||
| chr4:8294672 | C | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0119 others(5): Show |
8 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1051+471C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294672 | |||||||
| chr4:8294674 | A | ACTTATCC others(1016): Show |
1 | a0001c0001t0001g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1051+473_1051+474i others(1025): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294674 | |||||||
| chr4:8294675 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1051+474T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | |||||||
| chr4:8294675 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+474T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | |||||||
| chr4:8294675 | T | TACATCTG others(1111): Show |
1 | a0001c0001t0001g0119 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1051+474_1051+475i others(1120): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | |||||||
| chr4:8294675 | T | TACATCTG others(1112): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0120 others(4): Show |
9 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051+474_1051+475i others(1121): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | |||||||
| chr4:8294675 | T | TACATCTG others(1116): Show |
1 | a0001c0001t0001g0271 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1051+474_1051+475i others(1125): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294675 | |||||||
| chr4:8294675 | T | TCTGTCCA others(1108): Show |
6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0159 others(3): Show |
6 | HG01433.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+475_1051+476i others(1117): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294675 | ||||||
| chr4:8294678 | A | ACTTATCC others(1012): Show |
1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+477_1051+478i others(1021): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294678 | |||||||
| chr4:8294679 | T | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+478T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294679 | |||||||
| chr4:8294683 | T | TCTATCCA others(972): Show |
1 | a0001c0001t0001g0258 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1051+483_1051+484i others(981): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294683 | ||||||
| chr4:8294716 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1051+515T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294716 | |||||||
| chr4:8294770 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0342 a0001c0001t0011g0343 others(2): Show |
6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+569C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8294770 | |||||||
| chr4:8294801 | T | TCCAC | 131 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1051+612_1051+615d others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8294801 | ||||||
| chr4:8295055 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1051+854A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295055 | |||||||
| chr4:8295194 | C | T | 3 | a0001c0001t0004g0188 a0001c0001t0010g0037 a0002c0002t0001g0069 |
3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+993C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295194 | |||||||
| chr4:8295334 | G | T | 3 | a0001c0001t0004g0188 a0001c0001t0010g0037 a0002c0002t0001g0069 |
3 | HG02451.hp1 HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+1133G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295334 | |||||||
| chr4:8295433 | G | A | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+1232G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295433 | |||||||
| chr4:8295843 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051+1642G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8295843 | |||||||
| chr4:8296043 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
104 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1051+1842A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296043 | |||||||
| chr4:8296120 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1051+1919G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296120 | |||||||
| chr4:8296143 | A | G | 1 | a0001c0001t0010g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1051+1942A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296143 | |||||||
| chr4:8296152 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1051+1951G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296152 | |||||||
| chr4:8296219 | G | A | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+2018G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296219 | |||||||
| chr4:8296269 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1051+2068A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296269 | |||||||
| chr4:8296330 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0085 others(1): Show |
6 | HG01070.hp2 HG01255.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1051+2129C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296330 | |||||||
| chr4:8296357 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+2156C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296357 | |||||||
| chr4:8296557 | G | T | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+2356G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296557 | |||||||
| chr4:8296562 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1051+2361T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296562 | |||||||
| chr4:8296563 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+2362G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296563 | |||||||
| chr4:8296589 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0004g0188 a0001c0001t0016g0088 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051+2388T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296589 | |||||||
| chr4:8296891 | T | C | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+2690T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296891 | |||||||
| chr4:8296897 | A | T | 2 | a0001c0001t0001g0187 a0002c0002t0009g0061 |
2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1051+2696A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296897 | |||||||
| chr4:8296977 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051+2776T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296977 | |||||||
| chr4:8296993 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01361.hp2 HG03490.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051+2792G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8296993 | |||||||
| chr4:8297170 | G | A | 16 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0051 others(13): Show |
18 | HG00423.hp1 HG01433.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1051+2969G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297170 | |||||||
| chr4:8297171 | C | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0051 others(13): Show |
18 | HG00423.hp1 HG01433.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.1051+2970C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297171 | |||||||
| chr4:8297227 | G | A | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+3026G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297227 | |||||||
| chr4:8297382 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1051+3181G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297382 | |||||||
| chr4:8297435 | T | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
97 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1051+3234T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297435 | |||||||
| chr4:8297440 | GCCAGAGG others(9): Show |
G | 1 | a0001c0001t0001g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1051+3242_1051+325 others(20): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8297440 | ||||||
| chr4:8297495 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02135.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1051+3294G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297495 | |||||||
| chr4:8297563 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0340 a0001c0001t0001g0348 |
3 | NA18948.hp1 NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1051+3362G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297563 | |||||||
| chr4:8297587 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0063 |
2 | HG00642.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1051+3386G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297587 | |||||||
| chr4:8297619 | C | T | 2 | a0001c0001t0006g0333 a0001c0001t0006g0334 |
2 | NA18967.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1051+3418C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297619 | |||||||
| chr4:8297740 | C | A | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1051+3539C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297740 | |||||||
| chr4:8297840 | C | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(11): Show |
16 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1051+3639C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297840 | |||||||
| chr4:8297849 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1051+3648G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297849 | |||||||
| chr4:8297856 | G | A | 1 | a0003c0007t0001g0326 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1051+3655G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297856 | |||||||
| chr4:8297869 | A | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(10): Show |
15 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1051+3668A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297869 | |||||||
| chr4:8297892 | T | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1051+3691T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297892 | |||||||
| chr4:8297913 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(10): Show |
15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1051+3712C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297913 | |||||||
| chr4:8297993 | C | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
269 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1051+3792C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8297993 | |||||||
| chr4:8298000 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(16): Show |
20 | HG00423.hp1 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051+3799A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298000 | |||||||
| chr4:8298078 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1051+3877C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298078 | |||||||
| chr4:8298134 | A | G | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1051+3933A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298134 | |||||||
| chr4:8298138 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(9): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051+3937T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298138 | |||||||
| chr4:8298181 | C | T | 1 | a0001c0001t0018g0249 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1051+3980C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298181 | |||||||
| chr4:8298310 | T | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1051+4109T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298310 | |||||||
| chr4:8298474 | T | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3989T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298474 | |||||||
| chr4:8298519 | G | GT | 239 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
258 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1052-3933dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8298519 | ||||||
| chr4:8298709 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | NA18973.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1052-3754G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298709 | |||||||
| chr4:8298788 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0329 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1052-3675G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298788 | |||||||
| chr4:8298792 | C | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0132 others(3): Show |
6 | HG02818.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1052-3671C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298792 | |||||||
| chr4:8298850 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1052-3613T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298850 | |||||||
| chr4:8298866 | C | T | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3597C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8298866 | |||||||
| chr4:8299069 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1052-3394T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299069 | |||||||
| chr4:8299182 | G | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3281G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299182 | |||||||
| chr4:8299264 | T | G | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3199T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299264 | |||||||
| chr4:8299303 | T | G | 1 | a0001c0001t0001g0020 | 2 | HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.1052-3160T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299303 | |||||||
| chr4:8299364 | T | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-3099T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299364 | |||||||
| chr4:8299397 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1052-3066T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299397 | |||||||
| chr4:8299548 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1052-2915G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299548 | |||||||
| chr4:8299619 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
255 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1052-2844A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299619 | |||||||
| chr4:8299654 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1052-2809T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299654 | |||||||
| chr4:8299749 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1052-2714G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299749 | |||||||
| chr4:8299841 | C | CA | 130 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0020 others(127): Show |
137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1052-2622_1052-262 others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299841 | |||||||
| chr4:8299841 | C | CAT | 4 | a0001c0001t0001g0024 a0001c0001t0001g0259 a0001c0001t0001g0312 others(1): Show |
5 | HG02135.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-2622_1052-262 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299841 | |||||||
| chr4:8299841 | C | CT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
105 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1052-2606dupT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8299841 | ||||||
| chr4:8299842 | T | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0341 a0001c0001t0003g0161 others(4): Show |
7 | HG01109.hp2 HG02257.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1052-2621T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299842 | |||||||
| chr4:8299843 | T | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-2620T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299843 | |||||||
| chr4:8299913 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(10): Show |
15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1052-2550C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299913 | |||||||
| chr4:8299926 | A | G | 134 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0020 others(131): Show |
142 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1052-2537A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299926 | |||||||
| chr4:8299966 | C | T | 5 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0201 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-2497C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8299966 | |||||||
| chr4:8300021 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0182 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-2442G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300021 | |||||||
| chr4:8300263 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1052-2200G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300263 | |||||||
| chr4:8300414 | T | C | 1 | a0001c0001t0010g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1052-2049T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300414 | |||||||
| chr4:8300437 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0258 a0001c0001t0001g0276 others(4): Show |
7 | NA18942.hp1 NA18951.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052-2026T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300437 | |||||||
| chr4:8300509 | C | T | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1954C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300509 | |||||||
| chr4:8300516 | A | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1947A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300516 | |||||||
| chr4:8300542 | T | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
110 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.1052-1921T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300542 | |||||||
| chr4:8300547 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1052-1916C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300547 | |||||||
| chr4:8300602 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1052-1861T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300602 | |||||||
| chr4:8300671 | CTTTA | C | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0008c0012t0001g0244 |
3 | HG02135.hp2 NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1052-1788_1052-178 others(8): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300671 | ||||||
| chr4:8300744 | CATTG | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0001g0120 others(5): Show |
9 | HG00423.hp1 HG02015.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1052-1715_1052-171 others(8): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300744 | ||||||
| chr4:8300827 | C | T | 2 | a0001c0001t0001g0279 a0002c0002t0001g0127 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1052-1636C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300827 | |||||||
| chr4:8300852 | C | T | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1611C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300852 | |||||||
| chr4:8300895 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0194 a0001c0001t0001g0269 others(1): Show |
4 | HG01109.hp1 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052-1568T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8300895 | |||||||
| chr4:8300985 | A | ATTATTGA others(13): Show |
1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1452_1052-143 others(24): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8300985 | ||||||
| chr4:8301037 | TCA | T | 140 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(137): Show |
149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1052-1422_1052-142 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301037 | ||||||
| chr4:8301131 | ACT | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(14): Show |
19 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1052-1329_1052-132 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301131 | ||||||
| chr4:8301165 | A | ACT | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(314): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1052-1297_1052-129 others(6): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301165 | ||||||
| chr4:8301165 | A | T | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1052-1298A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301165 | |||||||
| chr4:8301168 | T | C | 2 | a0001c0001t0001g0279 a0002c0002t0009g0061 |
2 | HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1052-1295T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301168 | |||||||
| chr4:8301186 | TTTA | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0110 a0001c0001t0001g0121 others(1): Show |
5 | HG01361.hp2 HG03490.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1052-1274_1052-127 others(7): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301186 | ||||||
| chr4:8301234 | ATTATTGA others(13): Show |
A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
124 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1052-1211_1052-119 others(24): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301234 | ||||||
| chr4:8301238 | T | A | 138 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(135): Show |
147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.1052-1225T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301238 | |||||||
| chr4:8301254 | T | G | 4 | a0001c0001t0001g0341 a0001c0001t0003g0161 a0001c0001t0003g0346 others(1): Show |
4 | HG02257.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-1209T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301254 | |||||||
| chr4:8301257 | A | T | 4 | a0001c0001t0001g0341 a0001c0001t0003g0161 a0001c0001t0003g0346 others(1): Show |
4 | HG02257.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1052-1206A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301257 | |||||||
| chr4:8301262 | TTCACACT others(16): Show |
T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0165 |
2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1052-1178_1052-115 others(27): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301262 | ||||||
| chr4:8301285 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1052-1178G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301285 | |||||||
| chr4:8301285 | GTCACACT others(16): Show |
G | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-1155_1052-113 others(27): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 8301285 | ||||||
| chr4:8301412 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
125 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.1052-1051A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301412 | |||||||
| chr4:8301489 | T | G | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1052-974T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301489 | |||||||
| chr4:8301615 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0005g0122 a0001c0001t0005g0321 |
3 | HG02738.hp1 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1052-848C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301615 | |||||||
| chr4:8301632 | G | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052-831G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301632 | |||||||
| chr4:8301830 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(249): Show |
273 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1052-633G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301830 | |||||||
| chr4:8301872 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1052-591A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301872 | |||||||
| chr4:8301877 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1052-586A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8301877 | |||||||
| chr4:8302014 | C | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0351 |
2 | NA18972.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1052-449C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302014 | |||||||
| chr4:8302311 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(292): Show |
319 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.1052-152T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302311 | |||||||
| chr4:8302325 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1052-138A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302325 | |||||||
| chr4:8302370 | G | T | 138 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(135): Show |
148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1052-93G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302370 | |||||||
| chr4:8302387 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0286 |
2 | HG00438.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1052-76C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302387 | |||||||
| chr4:8302407 | A | G | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1052-56A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302407 | |||||||
| chr4:8302408 | G | A | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1052-55G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302408 | |||||||
| chr4:8302410 | G | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
98 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1052-53G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302410 | |||||||
| chr4:8302436 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0251 |
2 | HG02293.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1052-27C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302436 | |||||||
| chr4:8302444 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1052-19C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 6/8 | chr4 | 8302444 | |||||||
| chr4:8302670 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1100+159C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302670 | |||||||
| chr4:8302810 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0351 a0002c0002t0001g0127 |
3 | HG02922.hp2 NA18972.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1100+299G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302810 | |||||||
| chr4:8302929 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0348 |
2 | NA18948.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1100+418T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302929 | |||||||
| chr4:8302943 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(279): Show |
306 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.1100+432A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8302943 | |||||||
| chr4:8303087 | A | T | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1100+576A>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303087 | |||||||
| chr4:8303137 | G | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1100+626G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303137 | |||||||
| chr4:8303172 | C | T | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1100+661C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303172 | |||||||
| chr4:8303266 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0002g0038 a0001c0001t0002g0098 |
3 | HG03486.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1100+755C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303266 | |||||||
| chr4:8303318 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG01515.hp2 HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1100+807G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303318 | |||||||
| chr4:8303378 | G | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1101-806G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303378 | |||||||
| chr4:8303485 | G | A | 140 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(137): Show |
150 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1101-699G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303485 | |||||||
| chr4:8303512 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1101-672C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303512 | |||||||
| chr4:8303537 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-647T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303537 | |||||||
| chr4:8303742 | TTG | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(10): Show |
15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1101-440_1101-439d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303742 | ||||||
| chr4:8303776 | CCGTTCCG others(19): Show |
C | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1101-382_1101-357d others(28): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303776 | ||||||
| chr4:8303777 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-407C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303777 | |||||||
| chr4:8303802 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1101-382A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303802 | |||||||
| chr4:8303805 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-379T>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303805 | |||||||
| chr4:8303827 | TCC | T | 142 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(139): Show |
152 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1101-356_1101-355d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303827 | |||||||
| chr4:8303835 | A | G | 142 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(139): Show |
152 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1101-349A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303835 | |||||||
| chr4:8303900 | T | C | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1101-284T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8303900 | |||||||
| chr4:8303900 | T | TCATCCAT others(1): Show |
4 | a0001c0001t0001g0341 a0001c0001t0003g0161 a0001c0001t0003g0183 others(1): Show |
4 | HG01109.hp2 HG02257.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1101-262_1101-255d others(10): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 8303900 | ||||||
| chr4:8304054 | G | T | 138 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(135): Show |
148 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1101-130G>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 7/8 | chr4 | 8304054 | |||||||
| chr4:8304301 | C | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(141): Show |
155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1196+22C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304301 | |||||||
| chr4:8304319 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0034 others(10): Show |
15 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+40G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304319 | |||||||
| chr4:8304339 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1196+60G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304339 | |||||||
| chr4:8304364 | T | C | 144 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(141): Show |
155 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1196+85T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304364 | |||||||
| chr4:8304369 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1196+90C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304369 | |||||||
| chr4:8304414 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1196+135T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304414 | |||||||
| chr4:8304437 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0104 |
3 | HG01358.hp2 HG01943.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1196+158A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304437 | |||||||
| chr4:8304534 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1196+255A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304534 | |||||||
| chr4:8304572 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG01515.hp2 HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1196+293G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304572 | |||||||
| chr4:8304608 | T | C | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+329T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304608 | |||||||
| chr4:8304610 | C | T | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+331C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304610 | |||||||
| chr4:8304622 | G | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(142): Show |
156 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1196+343G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304622 | |||||||
| chr4:8304643 | GT | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
86 | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(83): Show |
intron_variant | MODIFIER | c.1196+395delT | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTT | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(78): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1196+394_1196+395d others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTTT | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0119 a0001c0001t0001g0123 others(8): Show |
12 | HG00423.hp1 HG02027.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1196+393_1196+395d others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0314 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1196+384_1196+395d others(14): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02572.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1196+383_1196+395d others(15): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0003g0161 a0001c0001t0007g0177 |
2 | HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1196+382_1196+395d others(16): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304643 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+381_1196+395d others(17): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304643 | ||||||
| chr4:8304648 | T | TTG | 48 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
54 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(4): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 8304648 | ||||||
| chr4:8304649 | T | TG | 78 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(75): Show |
83 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(3): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304649 | |||||||
| chr4:8304649 | T | TGTG | 13 | a0001c0001t0001g0103 a0001c0001t0001g0193 a0001c0001t0001g0202 others(10): Show |
13 | HG00408.hp2 HG00558.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.1196+370_1196+371i others(5): Show |
HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304649 | |||||||
| chr4:8304650 | T | G | 52 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(49): Show |
58 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1196+371T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304650 | |||||||
| chr4:8304651 | T | G | 79 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(76): Show |
84 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(81): Show |
intron_variant | MODIFIER | c.1196+372T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304651 | |||||||
| chr4:8304652 | T | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0141 a0001c0001t0001g0206 others(1): Show |
4 | HG00323.hp1 HG03654.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+373T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304652 | |||||||
| chr4:8304653 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1196+374T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304653 | |||||||
| chr4:8304654 | T | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0316 |
2 | HG00738.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1196+375T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304654 | |||||||
| chr4:8304655 | T | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
30 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(27): Show |
intron_variant | MODIFIER | c.1196+376T>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304655 | |||||||
| chr4:8304701 | C | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(175): Show |
193 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1196+422C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304701 | |||||||
| chr4:8304791 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1196+512G>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304791 | |||||||
| chr4:8304896 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1196+617C>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8304896 | |||||||
| chr4:8305026 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1196+747A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305026 | |||||||
| chr4:8305055 | A | C | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+776A>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305055 | |||||||
| chr4:8305056 | C | A | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1196+777C>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305056 | |||||||
| chr4:8305061 | T | C | 149 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(146): Show |
160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1196+782T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305061 | |||||||
| chr4:8305221 | G | A | 2 | a0001c0001t0004g0188 a0002c0002t0001g0069 |
2 | HG02451.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1197-750G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305221 | |||||||
| chr4:8305247 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0182 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-724G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305247 | |||||||
| chr4:8305292 | G | A | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-679G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305292 | |||||||
| chr4:8305331 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1197-640A>G | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305331 | |||||||
| chr4:8305357 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0216 |
2 | NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1197-614C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305357 | |||||||
| chr4:8305364 | C | T | 1 | a0001c0001t0016g0088 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1197-607C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305364 | |||||||
| chr4:8305394 | C | T | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-577C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305394 | |||||||
| chr4:8305513 | T | C | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1197-458T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305513 | |||||||
| chr4:8305515 | C | T | 1 | a0001c0001t0003g0346 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1197-456C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305515 | |||||||
| chr4:8305580 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1197-391C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305580 | |||||||
| chr4:8305596 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1197-375C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305596 | |||||||
| chr4:8305650 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1197-321C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305650 | |||||||
| chr4:8305674 | T | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | NA18949.hp2 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197-297T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305674 | |||||||
| chr4:8305753 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01934.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1197-218C>T | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305753 | |||||||
| chr4:8305777 | G | A | 135 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(132): Show |
145 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1197-194G>A | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305777 | |||||||
| chr4:8305811 | T | C | 1 | a0002c0002t0009g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-160T>C | HTRA3 | ENSG00000170801.10 | transcript | ENST00000307358.7 | protein_coding | 8/8 | chr4 | 8305811 |