Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1842 |
| ensemblid | ENSG00000106823.13 |
| hgncid | 3154 |
| symbol | ECM2 |
| name | extracellular matrix protein 2 |
| refseq_nuc | NM_001393.4 |
| refseq_prot | NP_001384.1 |
| ensembl_nuc | ENST00000344604.10 |
| ensembl_prot | ENSP00000344758.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 92495315 |
| end | 92535990 |
| strand | - |
| ver | v1.2 |
| region | chr9:92495315-92535990 |
| region5000 | chr9:92490315-92540990 |
| regionname0 | ECM2_chr9_92495315_92535990 |
| regionname5000 | ECM2_chr9_92490315_92540990 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 699 | 269 | 71 | 45 | 117 | 11 | 24 | 93 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0002 | 1/0 | 699 | 96 | 5 | 25 | 50 | 4 | 11 | 44 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0003 | 0/0 | 699 | 20 | 1 | 1 | 13 | 1 | 4 | 11 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0004 | 0/0 | 699 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0005 | 0/0 | 699 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0006 | 0/0 | 699 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0007 | 0/0 | 699 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0008 | 0/0 | 699 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0009 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0010 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0011 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| a0012 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | MKIAV others(694): Show |
chr9 | 92490315 | 92540990 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2097 | 129 | 6 | 25 | 80 | 4 | 13 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0002 | 0/0 | 2097 | 111 | 49 | 15 | 37 | 7 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0005 | 0/0 | 2097 | 9 | 7 | 2 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0006 | 0/0 | 2097 | 6 | 1 | 2 | 0 | 0 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0008 | 0/0 | 2097 | 4 | 0 | 0 | 0 | 0 | 4 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0009 | 0/0 | 2097 | 4 | 3 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0011 | 0/0 | 2097 | 3 | 3 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0017 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0018 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0001c0023 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0002c0003 | 1/0 | 2097 | 88 | 0 | 25 | 47 | 4 | 11 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0002c0007 | 0/0 | 2097 | 5 | 5 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0002c0010 | 0/0 | 2097 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0003c0004 | 0/0 | 2097 | 20 | 1 | 1 | 13 | 1 | 4 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0004c0015 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0004c0024 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0005c0014 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0006c0012 | 0/0 | 2097 | 2 | 0 | 0 | 0 | 2 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0007c0013 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0008c0020 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0008c0025 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0009c0021 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0010c0022 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0011c0019 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 | ||
| a0012c0016 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATGAA others(2092): Show |
chr9 | 92490315 | 92540990 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3185 | 129 | 6 | 25 | 80 | 4 | 13 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0002t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0002t0002 | 0/0 | 3185 | 108 | 46 | 15 | 37 | 7 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0002t0004 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0002t0005 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0005t0001 | 0/0 | 3185 | 9 | 7 | 2 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0006t0001 | 0/0 | 3185 | 6 | 1 | 2 | 0 | 0 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0008t0002 | 0/0 | 3185 | 4 | 0 | 0 | 0 | 0 | 4 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0009t0002 | 0/0 | 3185 | 4 | 3 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0011t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0017t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0018t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0001c0023t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0002c0003t0001 | 1/0 | 3185 | 88 | 0 | 25 | 47 | 4 | 11 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0002c0007t0001 | 0/0 | 3185 | 5 | 5 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0002c0010t0002 | 0/0 | 3185 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0003c0004t0002 | 0/0 | 3185 | 19 | 1 | 1 | 13 | 1 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0003c0004t0007 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0004c0015t0003 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0004c0024t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0005c0014t0002 | 0/0 | 3185 | 2 | 0 | 2 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0006c0012t0001 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 2 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0007c0013t0002 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0008c0020t0002 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0008c0025t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0009c0021t0006 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0010c0022t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0011c0019t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| a0012c0016t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | ATTTT others(3180): Show |
chr9 | 92490315 | 92540990 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 1 | 13 | 25 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 5 | 5 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 2 | 0 | 4 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0049 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0008 | 0/0 | 5 | 0 | 2 | 1 | 2 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0002t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0005t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0006t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0006t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0006t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0008t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0008t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0008t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0009t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0009t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0011t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0011t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0017t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0018t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0001c0023t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0002 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0005 | 1/0 | 10 | 0 | 5 | 1 | 0 | 3 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0007 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0007t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0007t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0010t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0010t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0002c0010t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0016 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0003c0004t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0004c0015t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0004c0015t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0004c0024t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0005c0014t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0005c0014t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0006c0012t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0007c0013t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0007c0013t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0008c0020t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0008c0025t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0009c0021t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0010c0022t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0011c0019t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| a0012c0016t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0030 | EUR | GBR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0142 | EUR | GBR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00280 | hp1 | a0003 | c0004 | t0002 | g0016 | EUR | FIN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0002 | EUR | FIN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0029 | EUR | FIN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00642 | hp1 | a0009 | c0021 | t0006 | g0073 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0189 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0170 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0179 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0162 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01081 | hp1 | a0001 | c0005 | t0001 | g0050 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01081 | hp2 | a0001 | c0009 | t0002 | g0139 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0175 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01168 | hp1 | a0005 | c0014 | t0002 | g0053 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01169 | hp2 | a0005 | c0014 | t0002 | g0052 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01255 | hp2 | a0001 | c0005 | t0001 | g0021 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0157 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0079 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0158 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0177 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01346 | hp1 | a0003 | c0004 | t0002 | g0026 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0178 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01358 | hp1 | a0001 | c0006 | t0001 | g0028 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01361 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01515 | hp1 | a0006 | c0012 | t0001 | g0043 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0037 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0082 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01517 | hp1 | a0006 | c0012 | t0001 | g0043 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0008 | EUR | IBS | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0151 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0150 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0192 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02015 | hp1 | a0003 | c0004 | t0002 | g0070 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02055 | hp1 | a0004 | c0015 | t0003 | g0076 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0166 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02165 | hp1 | a0003 | c0004 | t0002 | g0067 | EAS | CDX | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02257 | hp1 | a0004 | c0015 | t0003 | g0077 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02257 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02300 | hp2 | a0001 | c0006 | t0001 | g0028 | AMR | PEL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02615 | hp2 | a0002 | c0007 | t0001 | g0232 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02622 | hp1 | a0007 | c0013 | t0002 | g0096 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0153 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0005 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02698 | hp1 | a0001 | c0008 | t0002 | g0036 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02717 | hp2 | a0001 | c0009 | t0002 | g0018 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02723 | hp1 | a0001 | c0023 | t0001 | g0211 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02723 | hp2 | a0007 | c0013 | t0002 | g0097 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02735 | hp2 | a0001 | c0008 | t0002 | g0036 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0135 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0106 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0156 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02886 | hp1 | a0002 | c0007 | t0001 | g0015 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02895 | hp1 | a0001 | c0005 | t0001 | g0041 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02895 | hp2 | a0001 | c0009 | t0002 | g0018 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0114 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0041 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0103 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0155 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03017 | hp2 | a0004 | c0024 | t0001 | g0223 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03130 | hp2 | a0008 | c0025 | t0001 | g0121 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03139 | hp1 | a0010 | c0022 | t0001 | g0111 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0088 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03195 | hp1 | a0011 | c0019 | t0001 | g0101 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03225 | hp1 | a0002 | c0007 | t0001 | g0015 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0107 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03453 | hp2 | a0001 | c0017 | t0001 | g0143 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0134 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0002 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03490 | hp2 | a0001 | c0006 | t0001 | g0027 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03492 | hp1 | a0001 | c0006 | t0001 | g0027 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03540 | hp1 | a0001 | c0009 | t0002 | g0018 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0119 | AFR | GWD | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0110 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0108 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0045 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03688 | hp2 | a0001 | c0008 | t0002 | g0138 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0190 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03710 | hp1 | a0003 | c0004 | t0007 | g0054 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03831 | hp1 | a0003 | c0004 | t0002 | g0066 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0005 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0005 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03942 | hp2 | a0003 | c0004 | t0002 | g0056 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04115 | hp1 | a0001 | c0006 | t0001 | g0071 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04115 | hp2 | a0003 | c0004 | t0002 | g0060 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04184 | hp1 | a0001 | c0008 | t0002 | g0128 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04184 | hp2 | a0001 | c0018 | t0001 | g0090 | SAS | BEB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG04228 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | STU | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18522 | hp2 | a0002 | c0007 | t0001 | g0015 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18906 | hp1 | a0001 | c0011 | t0001 | g0032 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18906 | hp2 | a0002 | c0007 | t0001 | g0015 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18943 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0167 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18948 | hp1 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18951 | hp1 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0174 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0185 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0176 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18963 | hp2 | a0003 | c0004 | t0002 | g0055 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18973 | hp2 | a0003 | c0004 | t0002 | g0057 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18975 | hp2 | a0008 | c0020 | t0002 | g0131 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18977 | hp1 | a0002 | c0010 | t0002 | g0169 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18980 | hp2 | a0003 | c0004 | t0002 | g0062 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18984 | hp1 | a0003 | c0004 | t0002 | g0064 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0161 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18985 | hp1 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18992 | hp2 | a0012 | c0016 | t0001 | g0172 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18993 | hp2 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18995 | hp2 | a0003 | c0004 | t0002 | g0016 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19001 | hp2 | a0003 | c0004 | t0002 | g0016 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19012 | hp2 | a0002 | c0010 | t0002 | g0168 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19030 | hp2 | a0001 | c0011 | t0001 | g0102 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0072 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19055 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19056 | hp1 | a0002 | c0010 | t0002 | g0160 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19059 | hp2 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19075 | hp1 | a0003 | c0004 | t0002 | g0069 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19075 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19078 | hp2 | a0003 | c0004 | t0002 | g0061 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19084 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19091 | hp2 | a0003 | c0004 | t0002 | g0026 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0154 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0100 | AFR | ASW | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0045 | EUR | TSI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0022 | EUR | TSI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0171 | EUR | TSI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | GIH | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0005 | AMR | CLM | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02486 | hp1 | a0003 | c0004 | t0002 | g0058 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG02486 | hp2 | a0001 | c0011 | t0001 | g0032 | AFR | ACB | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | MSL | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0074 | AFR | USA | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | USA | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | USA | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0137 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | LWK | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0005 | REF | REF | ECM2_chr9_92490315_92540990 | ECM2 | chr9 | 92490315 | 92540990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92496352 | T | C | 1 | a0012 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.2063A>G | p.Tyr688Cys | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 2148/3185 | 2063/2100 | 688/699 | chr9 | 92496352 | |||
| chr9:92496457 | T | C | 1 | a0009 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1958A>G | p.Asn653Ser | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 2043/3185 | 1958/2100 | 653/699 | chr9 | 92496457 | |||
| chr9:92502596 | A | T | 1 | a0011 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1521T>A | p.His507Gln | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/10 | 1606/3185 | 1521/2100 | 507/699 | chr9 | 92502596 | |||
| chr9:92509932 | T | G | 1 | a0007 | 2 | HG02622.hp1 HG02723.hp2 |
missense_variant | MODERATE | c.1273A>C | p.Asn425His | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/10 | 1358/3185 | 1273/2100 | 425/699 | chr9 | 92509932 | |||
| chr9:92510015 | C | T | 2 | a0004 a0006 |
5 | HG01515.hp1 HG01517.hp1 HG02055.hp1 others(2): Show |
missense_variant | MODERATE | c.1190G>A | p.Arg397His | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/10 | 1275/3185 | 1190/2100 | 397/699 | chr9 | 92510015 | |||
| chr9:92510019 | T | A | 1 | a0005 | 2 | HG01168.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.1186A>T | p.Met396Leu | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/10 | 1271/3185 | 1186/2100 | 396/699 | chr9 | 92510019 | |||
| chr9:92514742 | G | A | 1 | a0008 | 2 | HG03130.hp2 NA18975.hp2 |
missense_variant | MODERATE | c.943C>T | p.Arg315Cys | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/10 | 1028/3185 | 943/2100 | 315/699 | chr9 | 92514742 | |||
| chr9:92514865 | C | G | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.820G>C | p.Asp274His | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/10 | 905/3185 | 820/2100 | 274/699 | chr9 | 92514865 | |||
| chr9:92515021 | C | T | 1 | a0010 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.664G>A | p.Glu222Lys | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/10 | 749/3185 | 664/2100 | 222/699 | chr9 | 92515021 | |||
| chr9:92515074 | C | T | 3 | a0003 a0005 a0009 |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
missense_variant | MODERATE | c.611G>A | p.Arg204Gln | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/10 | 696/3185 | 611/2100 | 204/699 | chr9 | 92515074 | |||
| chr9:92522700 | T | G | 9 | a0001 a0003 a0004 others(6): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.167A>C | p.Gln56Pro | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/10 | 252/3185 | 167/2100 | 56/699 | chr9 | 92522700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92505656 | T | C | 3 | a0001c0005 a0001c0011 a0011c0019 |
13 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(10): Show |
synonymous_variant | LOW | c.1341A>G | p.Gly447Gly | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/10 | 1426/3185 | 1341/2100 | 447/699 | chr9 | 92505656 | |||
| chr9:92509918 | G | A | 1 | a0001c0009 | 4 | HG01081.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
synonymous_variant | LOW | c.1287C>T | p.Ile429Ile | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/10 | 1372/3185 | 1287/2100 | 429/699 | chr9 | 92509918 | |||
| chr9:92512056 | A | G | 12 | a0001c0002 a0001c0006 a0001c0008 others(9): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
synonymous_variant | LOW | c.1125T>C | p.Ser375Ser | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/10 | 1210/3185 | 1125/2100 | 375/699 | chr9 | 92512056 | |||
| chr9:92512059 | C | T | 2 | a0001c0017 a0001c0023 |
2 | HG02723.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.1122G>A | p.Leu374Leu | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/10 | 1207/3185 | 1122/2100 | 374/699 | chr9 | 92512059 | |||
| chr9:92514863 | A | G | 1 | a0002c0007 | 5 | HG02615.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
synonymous_variant | LOW | c.822T>C | p.Asp274Asp | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/10 | 907/3185 | 822/2100 | 274/699 | chr9 | 92514863 | |||
| chr9:92517688 | A | G | 1 | a0001c0008 | 4 | HG02698.hp1 HG02735.hp2 HG03688.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.480T>C | p.Thr160Thr | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/10 | 565/3185 | 480/2100 | 160/699 | chr9 | 92517688 | |||
| chr9:92517703 | C | A | 9 | a0001c0002 a0001c0008 a0001c0009 others(6): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
synonymous_variant | LOW | c.465G>T | p.Pro155Pro | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/10 | 550/3185 | 465/2100 | 155/699 | chr9 | 92517703 | |||
| chr9:92522591 | A | G | 9 | a0001c0002 a0001c0008 a0001c0009 others(6): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
synonymous_variant | LOW | c.276T>C | p.Ser92Ser | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/10 | 361/3185 | 276/2100 | 92/699 | chr9 | 92522591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92495746 | G | A | 1 | a0003c0004t0007 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 569 | chr9 | 92495746 | ||||||
| chr9:92495770 | A | G | 1 | a0001c0002t0004 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 545 | chr9 | 92495770 | ||||||
| chr9:92495837 | A | G | 13 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0005 others(10): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*478T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 478 | chr9 | 92495837 | ||||||
| chr9:92495904 | T | C | 1 | a0004c0015t0003 | 2 | HG02055.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*411A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 411 | chr9 | 92495904 | ||||||
| chr9:92496149 | C | T | 1 | a0009c0021t0006 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*166G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 166 | chr9 | 92496149 | ||||||
| chr9:92496159 | A | G | 2 | a0001c0002t0004 a0001c0002t0005 |
2 | HG03486.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*156T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 10/10 | 156 | chr9 | 92496159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:92496632 | C | A | 1 | a0001c0002t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1932-149G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92496632 | |||||||
| chr9:92496815 | CTT | C | 2 | a0001c0002t0002g0017 a0001c0002t0002g0118 |
4 | HG02145.hp1 HG02647.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-334_1932-333d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92496815 | |||||||
| chr9:92496940 | C | CA | 29 | a0001c0001t0001g0204 a0001c0001t0001g0233 a0001c0001t0001g0234 others(26): Show |
33 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1932-458dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92496940 | |||||||
| chr9:92497003 | A | G | 1 | a0001c0002t0002g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1932-520T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497003 | |||||||
| chr9:92497211 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1932-728A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497211 | |||||||
| chr9:92497297 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1932-814A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497297 | |||||||
| chr9:92497321 | T | C | 1 | a0001c0002t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1932-838A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497321 | |||||||
| chr9:92497350 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1932-867G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497350 | |||||||
| chr9:92497457 | T | C | 1 | a0001c0002t0002g0133 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1932-974A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497457 | |||||||
| chr9:92497583 | C | T | 2 | a0003c0004t0002g0057 a0003c0004t0002g0061 |
2 | NA18973.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1932-1100G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497583 | |||||||
| chr9:92497584 | G | A | 1 | a0002c0007t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1932-1101C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497584 | |||||||
| chr9:92497624 | C | CA | 10 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0083 others(7): Show |
15 | HG00597.hp1 HG02896.hp1 HG03453.hp1 others(12): Show |
intron_variant | MODIFIER | c.1932-1142dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497624 | |||||||
| chr9:92497719 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1932-1236T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497719 | |||||||
| chr9:92497734 | C | A | 20 | a0003c0004t0002g0016 a0003c0004t0002g0026 a0003c0004t0002g0055 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1932-1251G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497734 | |||||||
| chr9:92497874 | TA | T | 27 | a0001c0001t0001g0047 a0001c0001t0001g0194 a0001c0001t0001g0233 others(24): Show |
34 | HG01070.hp2 HG01074.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.1932-1392delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497874 | |||||||
| chr9:92497874 | TAA | T | 103 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(100): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1932-1393_1932-139 others(6): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497874 | |||||||
| chr9:92497874 | TAAA | T | 8 | a0001c0002t0002g0114 a0001c0002t0002g0132 a0001c0002t0002g0135 others(5): Show |
8 | HG01168.hp1 HG02809.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1932-1394_1932-139 others(7): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497874 | |||||||
| chr9:92497961 | C | G | 2 | a0001c0002t0002g0135 a0001c0002t0002g0136 |
2 | HG00733.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1932-1478G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497961 | |||||||
| chr9:92497988 | T | C | 1 | a0001c0002t0002g0087 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1932-1505A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92497988 | |||||||
| chr9:92498735 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1931+1992C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92498735 | |||||||
| chr9:92498738 | T | C | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1931+1989A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92498738 | |||||||
| chr9:92498822 | C | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0047 others(43): Show |
98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1931+1905G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92498822 | |||||||
| chr9:92498876 | T | G | 1 | a0001c0002t0002g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1931+1851A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92498876 | |||||||
| chr9:92498981 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1931+1746A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92498981 | |||||||
| chr9:92499045 | A | G | 111 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(108): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1931+1682T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499045 | |||||||
| chr9:92499195 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(27): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1931+1532A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499195 | |||||||
| chr9:92499202 | C | T | 1 | a0008c0025t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1931+1525G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499202 | |||||||
| chr9:92499322 | T | A | 1 | a0001c0002t0002g0030 | 2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1931+1405A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499322 | |||||||
| chr9:92499407 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1931+1320A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499407 | |||||||
| chr9:92499422 | T | C | 1 | a0001c0002t0002g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1931+1305A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499422 | |||||||
| chr9:92499685 | C | G | 4 | a0001c0002t0002g0040 a0001c0008t0002g0036 a0001c0008t0002g0128 others(1): Show |
6 | HG00639.hp2 HG02698.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1931+1042G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499685 | |||||||
| chr9:92499763 | G | T | 1 | a0003c0004t0002g0069 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1931+964C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499763 | |||||||
| chr9:92499825 | C | T | 49 | a0001c0002t0002g0010 a0001c0002t0002g0029 a0001c0002t0002g0030 others(46): Show |
57 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1931+902G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499825 | |||||||
| chr9:92499827 | A | G | 1 | a0003c0004t0002g0069 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1931+900T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499827 | |||||||
| chr9:92499829 | G | T | 1 | a0003c0004t0002g0069 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1931+898C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499829 | |||||||
| chr9:92499842 | T | C | 1 | a0003c0004t0002g0069 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1931+885A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92499842 | |||||||
| chr9:92500060 | C | G | 120 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(117): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1931+667G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500060 | |||||||
| chr9:92500339 | C | G | 3 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02622.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1931+388G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500339 | |||||||
| chr9:92500364 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1931+363C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500364 | |||||||
| chr9:92500465 | G | C | 9 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(6): Show |
13 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1931+262C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500465 | |||||||
| chr9:92500541 | A | G | 1 | a0001c0006t0001g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1931+186T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500541 | |||||||
| chr9:92500631 | C | A | 1 | a0001c0001t0001g0048 | 2 | NA18963.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1931+96G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500631 | |||||||
| chr9:92500654 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1931+73G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500654 | |||||||
| chr9:92500660 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1931+67T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 9/9 | chr9 | 92500660 | |||||||
| chr9:92501091 | A | G | 1 | a0002c0003t0001g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1605-38T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92501091 | |||||||
| chr9:92501125 | G | C | 1 | a0002c0003t0001g0007 | 6 | HG00639.hp1 HG01069.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605-72C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92501125 | |||||||
| chr9:92501224 | A | C | 1 | a0001c0002t0002g0084 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1605-171T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92501224 | |||||||
| chr9:92501231 | T | C | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1605-178A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92501231 | |||||||
| chr9:92501798 | A | G | 1 | a0002c0003t0001g0171 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1604+715T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92501798 | |||||||
| chr9:92502056 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1604+457T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92502056 | |||||||
| chr9:92502082 | A | G | 1 | a0001c0002t0002g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1604+431T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92502082 | |||||||
| chr9:92502162 | T | A | 5 | a0001c0002t0001g0120 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
7 | HG01358.hp1 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1604+351A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92502162 | |||||||
| chr9:92502213 | G | A | 5 | a0001c0002t0001g0120 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
7 | HG01358.hp1 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1604+300C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92502213 | |||||||
| chr9:92502411 | G | A | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1604+102C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 8/9 | chr9 | 92502411 | |||||||
| chr9:92502804 | C | CT | 9 | a0001c0001t0001g0024 a0001c0001t0001g0219 a0001c0001t0001g0228 others(6): Show |
17 | HG00099.hp1 HG00741.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1465-153dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92502804 | |||||||
| chr9:92502804 | CT | C | 20 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0001g0229 others(17): Show |
25 | HG01074.hp1 HG01168.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.1465-153delA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92502804 | |||||||
| chr9:92502804 | CTT | C | 86 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(83): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1465-154_1465-153d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92502804 | |||||||
| chr9:92502846 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1465-194A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92502846 | |||||||
| chr9:92503059 | C | T | 3 | a0001c0011t0001g0032 a0001c0011t0001g0102 a0011c0019t0001g0101 |
4 | HG02486.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-407G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503059 | |||||||
| chr9:92503083 | C | T | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1465-431G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503083 | |||||||
| chr9:92503276 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1465-624G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503276 | |||||||
| chr9:92503298 | A | T | 111 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(108): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1465-646T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503298 | |||||||
| chr9:92503403 | G | C | 9 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(6): Show |
13 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1465-751C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503403 | |||||||
| chr9:92503602 | T | A | 2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1465-950A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503602 | |||||||
| chr9:92503726 | A | T | 1 | a0002c0003t0001g0022 | 3 | HG01433.hp1 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1465-1074T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92503726 | |||||||
| chr9:92504184 | T | TAAAAA | 20 | a0003c0004t0002g0016 a0003c0004t0002g0026 a0003c0004t0002g0055 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1464+1348_1464+134 others(9): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504184 | |||||||
| chr9:92504185 | C | A | 20 | a0003c0004t0002g0016 a0003c0004t0002g0026 a0003c0004t0002g0055 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1464+1348G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504185 | |||||||
| chr9:92504302 | C | G | 2 | a0002c0003t0001g0161 a0002c0003t0001g0165 |
2 | NA18980.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1464+1231G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504302 | |||||||
| chr9:92504320 | G | A | 20 | a0003c0004t0002g0016 a0003c0004t0002g0026 a0003c0004t0002g0055 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1464+1213C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504320 | |||||||
| chr9:92504485 | C | T | 3 | a0001c0002t0002g0017 a0001c0002t0002g0118 a0001c0002t0002g0119 |
5 | HG02145.hp1 HG02647.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464+1048G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504485 | |||||||
| chr9:92504530 | A | G | 113 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(110): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1464+1003T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504530 | |||||||
| chr9:92504769 | C | T | 1 | a0001c0002t0002g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1464+764G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504769 | |||||||
| chr9:92504830 | C | T | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1464+703G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504830 | |||||||
| chr9:92504855 | G | A | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1464+678C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504855 | |||||||
| chr9:92504869 | G | A | 1 | a0001c0002t0002g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1464+664C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504869 | |||||||
| chr9:92504875 | A | T | 1 | a0001c0002t0002g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1464+658T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92504875 | |||||||
| chr9:92505078 | A | G | 1 | a0003c0004t0002g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1464+455T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92505078 | |||||||
| chr9:92505278 | A | C | 120 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(117): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1464+255T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92505278 | |||||||
| chr9:92505424 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1464+109T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 7/9 | chr9 | 92505424 | |||||||
| chr9:92505829 | A | G | 1 | a0001c0002t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1307-139T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92505829 | |||||||
| chr9:92505912 | C | T | 1 | a0009c0021t0006g0073 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1307-222G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92505912 | |||||||
| chr9:92506299 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0198 a0001c0001t0001g0210 others(4): Show |
13 | HG00738.hp2 HG01361.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1307-609C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92506299 | |||||||
| chr9:92506325 | T | C | 1 | a0001c0002t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1307-635A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92506325 | |||||||
| chr9:92506385 | A | AT | 20 | a0003c0004t0002g0016 a0003c0004t0002g0026 a0003c0004t0002g0055 others(17): Show |
23 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-696dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92506385 | |||||||
| chr9:92506553 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1307-863G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92506553 | |||||||
| chr9:92507038 | T | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1307-1348A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507038 | |||||||
| chr9:92507110 | C | G | 1 | a0001c0002t0002g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1307-1420G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507110 | |||||||
| chr9:92507424 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1307-1734T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507424 | |||||||
| chr9:92507462 | A | G | 5 | a0001c0002t0001g0120 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
7 | HG01358.hp1 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-1772T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507462 | |||||||
| chr9:92507823 | G | A | 1 | a0001c0002t0002g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1306+2076C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507823 | |||||||
| chr9:92507850 | C | T | 1 | a0001c0002t0002g0146 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1306+2049G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92507850 | |||||||
| chr9:92508077 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1306+1822A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508077 | |||||||
| chr9:92508172 | T | C | 3 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02622.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1306+1727A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508172 | |||||||
| chr9:92508174 | C | T | 3 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02622.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1306+1725G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508174 | |||||||
| chr9:92508254 | G | A | 1 | a0001c0018t0001g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1306+1645C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508254 | |||||||
| chr9:92508268 | G | A | 9 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0123 others(6): Show |
14 | HG00597.hp1 NA18944.hp1 NA18947.hp2 others(11): Show |
intron_variant | MODIFIER | c.1306+1631C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508268 | |||||||
| chr9:92508499 | A | G | 91 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(88): Show |
124 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1306+1400T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92508499 | |||||||
| chr9:92509579 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1306+320A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 6/9 | chr9 | 92509579 | |||||||
| chr9:92510222 | A | G | 1 | a0002c0003t0001g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1171-188T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92510222 | |||||||
| chr9:92510717 | A | C | 5 | a0001c0002t0002g0034 a0001c0002t0002g0074 a0001c0002t0002g0113 others(2): Show |
6 | HG02145.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1171-683T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92510717 | |||||||
| chr9:92510731 | A | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(27): Show |
76 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1171-697T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92510731 | |||||||
| chr9:92510866 | A | G | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1171-832T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92510866 | |||||||
| chr9:92510946 | T | C | 2 | a0002c0007t0001g0015 a0002c0007t0001g0232 |
5 | HG02615.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1171-912A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92510946 | |||||||
| chr9:92511056 | T | G | 1 | a0003c0004t0002g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1170+955A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511056 | |||||||
| chr9:92511211 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1170+800G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511211 | |||||||
| chr9:92511212 | G | A | 1 | a0001c0002t0002g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1170+799C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511212 | |||||||
| chr9:92511368 | G | GC | 91 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(88): Show |
124 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1170+642dupG | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511368 | |||||||
| chr9:92511426 | GT | G | 21 | a0001c0002t0002g0118 a0003c0004t0002g0016 a0003c0004t0002g0026 others(18): Show |
24 | HG00280.hp1 HG00642.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1170+584delA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511426 | |||||||
| chr9:92511426 | GTT | G | 90 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(87): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1170+583_1170+584d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511426 | |||||||
| chr9:92511536 | A | C | 1 | a0001c0002t0002g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1170+475T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511536 | |||||||
| chr9:92511803 | T | C | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 |
5 | HG01358.hp1 HG02300.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+208A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511803 | |||||||
| chr9:92511979 | A | G | 111 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(108): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1170+32T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 5/9 | chr9 | 92511979 | |||||||
| chr9:92512182 | A | G | 1 | a0001c0002t0002g0116 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1055-56T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512182 | |||||||
| chr9:92512244 | C | G | 5 | a0001c0002t0001g0120 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
7 | HG01358.hp1 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055-118G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512244 | |||||||
| chr9:92512525 | G | A | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1055-399C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512525 | |||||||
| chr9:92512568 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1055-442G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512568 | |||||||
| chr9:92512742 | G | A | 119 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(116): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1055-616C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512742 | |||||||
| chr9:92512782 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0068 |
2 | HG00735.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1055-656C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92512782 | |||||||
| chr9:92513025 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1055-899G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92513025 | |||||||
| chr9:92513069 | G | C | 1 | a0002c0003t0001g0045 | 2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1055-943C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92513069 | |||||||
| chr9:92513886 | A | G | 1 | a0001c0002t0002g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1054+745T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92513886 | |||||||
| chr9:92513946 | G | A | 1 | a0001c0002t0002g0039 | 2 | NA18955.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.1054+685C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92513946 | |||||||
| chr9:92514001 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1054+630C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514001 | |||||||
| chr9:92514002 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1054+629G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514002 | |||||||
| chr9:92514124 | C | CT | 7 | a0001c0001t0001g0227 a0001c0011t0001g0032 a0001c0011t0001g0102 others(4): Show |
8 | HG02083.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1054+506dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514124 | |||||||
| chr9:92514124 | CT | C | 101 | a0001c0001t0001g0194 a0001c0001t0001g0208 a0001c0001t0001g0209 others(98): Show |
136 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1054+506delA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514124 | |||||||
| chr9:92514274 | C | CT | 13 | a0001c0001t0001g0210 a0001c0001t0001g0222 a0001c0002t0002g0011 others(10): Show |
18 | HG00597.hp1 HG01081.hp1 HG03492.hp2 others(15): Show |
intron_variant | MODIFIER | c.1054+356dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514274 | |||||||
| chr9:92514305 | C | T | 42 | a0001c0002t0002g0010 a0001c0002t0002g0029 a0001c0002t0002g0030 others(39): Show |
50 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1054+326G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514305 | |||||||
| chr9:92514555 | G | C | 4 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(1): Show |
6 | HG01358.hp1 HG02300.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1054+76C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514555 | |||||||
| chr9:92514603 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1054+28T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 4/9 | chr9 | 92514603 | |||||||
| chr9:92515232 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.482-29C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92515232 | |||||||
| chr9:92515375 | A | G | 1 | a0002c0003t0001g0167 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.482-172T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92515375 | |||||||
| chr9:92515747 | C | T | 1 | a0008c0025t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.482-544G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92515747 | |||||||
| chr9:92515839 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0196 |
4 | HG00609.hp1 HG02602.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-636T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92515839 | |||||||
| chr9:92515854 | G | C | 2 | a0001c0002t0004g0134 a0001c0002t0005g0108 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.482-651C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92515854 | |||||||
| chr9:92516067 | T | C | 1 | a0001c0006t0001g0028 | 2 | HG01358.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.482-864A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516067 | |||||||
| chr9:92516068 | T | C | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-865A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516068 | |||||||
| chr9:92516069 | T | C | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-866A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516069 | |||||||
| chr9:92516070 | T | C | 6 | a0001c0001t0001g0209 a0001c0006t0001g0027 a0001c0006t0001g0028 others(3): Show |
8 | HG00323.hp1 HG00642.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-867A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516070 | |||||||
| chr9:92516071 | T | C | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-868A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516071 | |||||||
| chr9:92516072 | T | C | 9 | a0001c0001t0001g0214 a0001c0006t0001g0027 a0001c0006t0001g0028 others(6): Show |
12 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.482-869A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516072 | |||||||
| chr9:92516072 | T | G | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.482-869A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516072 | |||||||
| chr9:92516072 | TC | T | 16 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0002c0003t0001g0190 others(13): Show |
19 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.482-870delG | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516072 | |||||||
| chr9:92516079 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.482-876G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516079 | |||||||
| chr9:92516086 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(24): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.482-883G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516086 | |||||||
| chr9:92516102 | C | G | 2 | a0002c0003t0001g0178 a0002c0003t0001g0192 |
2 | HG01346.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.482-899G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516102 | |||||||
| chr9:92516353 | G | A | 40 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(37): Show |
63 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.482-1150C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516353 | |||||||
| chr9:92516402 | A | G | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.482-1199T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516402 | |||||||
| chr9:92516432 | CTATA | C | 4 | a0001c0002t0004g0134 a0001c0009t0002g0018 a0001c0009t0002g0139 others(1): Show |
6 | HG01081.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-1233_482-1230d others(6): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516432 | |||||||
| chr9:92516603 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.481+1084T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516603 | |||||||
| chr9:92516707 | G | A | 1 | a0002c0003t0001g0184 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.481+980C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516707 | |||||||
| chr9:92516790 | A | C | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.481+897T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516790 | |||||||
| chr9:92516938 | T | C | 1 | a0001c0002t0002g0106 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.481+749A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516938 | |||||||
| chr9:92516980 | G | A | 2 | a0001c0002t0004g0134 a0001c0017t0001g0143 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.481+707C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92516980 | |||||||
| chr9:92517000 | G | T | 1 | a0002c0003t0001g0166 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.481+687C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517000 | |||||||
| chr9:92517014 | CAGA | C | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.481+670_481+672del others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517014 | |||||||
| chr9:92517088 | GA | G | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.481+598delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517088 | |||||||
| chr9:92517132 | T | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02027.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.481+555A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517132 | |||||||
| chr9:92517250 | G | C | 1 | a0001c0002t0002g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.481+437C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517250 | |||||||
| chr9:92517306 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.481+381T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 3/9 | chr9 | 92517306 | |||||||
| chr9:92518022 | A | G | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.293-147T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518022 | |||||||
| chr9:92518069 | C | T | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(42): Show |
70 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.293-194G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518069 | |||||||
| chr9:92518300 | G | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-425C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518300 | |||||||
| chr9:92518325 | A | G | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(42): Show |
70 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.293-450T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518325 | |||||||
| chr9:92518426 | G | A | 1 | a0001c0002t0002g0142 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.293-551C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518426 | |||||||
| chr9:92518624 | C | T | 49 | a0001c0002t0001g0120 a0001c0002t0002g0010 a0001c0002t0002g0029 others(46): Show |
58 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.293-749G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518624 | |||||||
| chr9:92518746 | G | A | 1 | a0008c0025t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.293-871C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518746 | |||||||
| chr9:92518960 | T | C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0136 |
2 | HG00733.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.293-1085A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92518960 | |||||||
| chr9:92519079 | T | C | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-1204A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92519079 | |||||||
| chr9:92519177 | A | G | 115 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(112): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.293-1302T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92519177 | |||||||
| chr9:92519192 | C | T | 1 | a0001c0002t0002g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-1317G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92519192 | |||||||
| chr9:92519196 | T | C | 1 | a0001c0002t0002g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-1321A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92519196 | |||||||
| chr9:92519948 | C | T | 3 | a0003c0004t0002g0057 a0003c0004t0002g0061 a0003c0004t0002g0062 |
3 | NA18973.hp2 NA18980.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.293-2073G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92519948 | |||||||
| chr9:92520049 | A | G | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.293-2174T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520049 | |||||||
| chr9:92520052 | A | AGGGAAGA others(304): Show |
1 | a0001c0002t0002g0033 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.293-2178_293-2177i others(313): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(309): Show |
1 | a0001c0017t0001g0143 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-2178_293-2177i others(318): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(315): Show |
2 | a0001c0002t0002g0082 a0001c0002t0002g0098 |
2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.293-2178_293-2177i others(324): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(316): Show |
47 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(44): Show |
68 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.293-2178_293-2177i others(325): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(316): Show |
1 | a0001c0002t0002g0035 | 2 | NA18942.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.293-2178_293-2177i others(325): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(317): Show |
1 | a0001c0002t0002g0099 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.293-2178_293-2177i others(326): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(317): Show |
30 | a0001c0002t0002g0010 a0001c0002t0002g0011 a0001c0002t0002g0020 others(27): Show |
41 | HG00597.hp1 HG00733.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.293-2178_293-2177i others(326): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520052 | A | AGGGAAGA others(318): Show |
11 | a0001c0002t0002g0086 a0001c0002t0002g0087 a0001c0002t0002g0091 others(8): Show |
11 | HG00735.hp2 HG01168.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-2178_293-2177i others(327): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520052 | |||||||
| chr9:92520245 | C | T | 2 | a0002c0003t0001g0161 a0002c0003t0001g0165 |
2 | NA18980.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.292+2330G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520245 | |||||||
| chr9:92520275 | C | T | 6 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(3): Show |
9 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+2300G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520275 | |||||||
| chr9:92520281 | T | C | 17 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(14): Show |
20 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.292+2294A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520281 | |||||||
| chr9:92520371 | C | T | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.292+2204G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520371 | |||||||
| chr9:92520624 | T | C | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.292+1951A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520624 | |||||||
| chr9:92520745 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.292+1830A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92520745 | |||||||
| chr9:92521260 | A | C | 3 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02622.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.292+1315T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521260 | |||||||
| chr9:92521260 | A | G | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.292+1315T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521260 | |||||||
| chr9:92521426 | G | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.292+1149C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521426 | |||||||
| chr9:92521529 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.292+1046T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521529 | |||||||
| chr9:92521605 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.292+970T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521605 | |||||||
| chr9:92521680 | T | G | 17 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(14): Show |
20 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.292+895A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521680 | |||||||
| chr9:92521930 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(47): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.292+645T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92521930 | |||||||
| chr9:92522065 | GTTGTTTT others(3): Show |
G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0002c0003t0001g0178 |
3 | HG01346.hp2 HG02027.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.292+500_292+509del others(10): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522065 | |||||||
| chr9:92522107 | G | T | 3 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02622.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.292+468C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522107 | |||||||
| chr9:92522109 | C | T | 1 | a0001c0018t0001g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.292+466G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522109 | |||||||
| chr9:92522110 | G | A | 1 | a0001c0002t0002g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.292+465C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522110 | |||||||
| chr9:92522146 | G | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0217 |
2 | HG02129.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.292+429C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522146 | |||||||
| chr9:92522148 | G | A | 2 | a0002c0003t0001g0023 a0002c0003t0001g0183 |
4 | NA18979.hp1 NA19075.hp2 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+427C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522148 | |||||||
| chr9:92522334 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.292+241G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522334 | |||||||
| chr9:92522381 | T | C | 1 | a0002c0003t0001g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.292+194A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522381 | |||||||
| chr9:92522410 | G | A | 1 | a0003c0004t0002g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.292+165C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522410 | |||||||
| chr9:92522493 | C | G | 1 | a0001c0002t0005g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.292+82G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 2/9 | chr9 | 92522493 | |||||||
| chr9:92522924 | G | T | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-31C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92522924 | |||||||
| chr9:92522940 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-27-47A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92522940 | |||||||
| chr9:92523050 | T | G | 1 | a0002c0003t0001g0184 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-27-157A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523050 | |||||||
| chr9:92523079 | C | CT | 8 | a0001c0001t0001g0197 a0001c0002t0002g0103 a0001c0006t0001g0027 others(5): Show |
10 | HG00642.hp1 HG01358.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27-187dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523079 | |||||||
| chr9:92523126 | G | A | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-27-233C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523126 | |||||||
| chr9:92523329 | G | T | 1 | a0001c0002t0002g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-27-436C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523329 | |||||||
| chr9:92523331 | G | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-27-438C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523331 | |||||||
| chr9:92523558 | C | T | 2 | a0002c0003t0001g0163 a0002c0003t0001g0186 |
2 | NA18948.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-27-665G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523558 | |||||||
| chr9:92523574 | A | G | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-27-681T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523574 | |||||||
| chr9:92523659 | G | C | 1 | a0001c0002t0002g0033 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-27-766C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523659 | |||||||
| chr9:92523725 | G | A | 1 | a0001c0002t0002g0100 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-27-832C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523725 | |||||||
| chr9:92523825 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-27-932G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523825 | |||||||
| chr9:92523847 | C | T | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-27-954G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523847 | |||||||
| chr9:92523897 | C | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-27-1004G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523897 | |||||||
| chr9:92523904 | T | C | 1 | a0003c0004t0002g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-27-1011A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523904 | |||||||
| chr9:92523922 | A | G | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(42): Show |
70 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.-27-1029T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523922 | |||||||
| chr9:92523940 | A | G | 1 | a0001c0002t0002g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-27-1047T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92523940 | |||||||
| chr9:92524034 | C | T | 1 | a0003c0004t0002g0063 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-27-1141G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92524034 | |||||||
| chr9:92524430 | C | T | 3 | a0002c0003t0001g0022 a0002c0003t0001g0162 a0006c0012t0001g0043 |
6 | HG01074.hp1 HG01433.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-1537G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92524430 | |||||||
| chr9:92524570 | A | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-27-1677T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92524570 | |||||||
| chr9:92524680 | C | T | 1 | a0001c0005t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27-1787G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92524680 | |||||||
| chr9:92524825 | T | C | 2 | a0002c0003t0001g0178 a0002c0003t0001g0192 |
2 | HG01346.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-27-1932A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92524825 | |||||||
| chr9:92525065 | C | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0217 |
2 | HG02129.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-27-2172G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525065 | |||||||
| chr9:92525185 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0196 |
4 | HG00609.hp1 HG02602.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-2292C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525185 | |||||||
| chr9:92525209 | TCAGGAGG others(6): Show |
T | 7 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0122 others(4): Show |
13 | NA18940.hp1 NA18951.hp2 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.-27-2329_-27-2317d others(15): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525209 | |||||||
| chr9:92525310 | T | C | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-27-2417A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525310 | |||||||
| chr9:92525313 | G | A | 1 | a0002c0003t0001g0179 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-27-2420C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525313 | |||||||
| chr9:92525317 | C | CA | 6 | a0001c0002t0002g0033 a0001c0011t0001g0032 a0001c0011t0001g0102 others(3): Show |
8 | HG02486.hp2 HG02976.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-2425dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525317 | |||||||
| chr9:92525356 | G | T | 2 | a0001c0002t0002g0126 a0001c0002t0002g0127 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-27-2463C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525356 | |||||||
| chr9:92525472 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-27-2579T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525472 | |||||||
| chr9:92525594 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-27-2701A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525594 | |||||||
| chr9:92525595 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-27-2702T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525595 | |||||||
| chr9:92525596 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-27-2703T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525596 | |||||||
| chr9:92525617 | G | A | 1 | a0003c0004t0002g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-27-2724C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525617 | |||||||
| chr9:92525735 | A | G | 42 | a0001c0002t0001g0120 a0001c0002t0002g0010 a0001c0002t0002g0029 others(39): Show |
51 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.-27-2842T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525735 | |||||||
| chr9:92525815 | G | A | 4 | a0003c0004t0002g0055 a0003c0004t0002g0063 a0003c0004t0002g0064 others(1): Show |
4 | NA18951.hp1 NA18963.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-2922C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525815 | |||||||
| chr9:92525837 | T | C | 1 | a0001c0002t0002g0105 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-27-2944A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525837 | |||||||
| chr9:92525871 | G | A | 9 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0005t0001g0021 others(6): Show |
12 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-27-2978C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525871 | |||||||
| chr9:92525893 | C | CA | 29 | a0001c0001t0001g0014 a0001c0001t0001g0218 a0001c0001t0001g0221 others(26): Show |
36 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-27-3001dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525893 | |||||||
| chr9:92525893 | CA | C | 7 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0002t0002g0087 others(4): Show |
7 | HG01168.hp2 HG02109.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-3001delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525893 | |||||||
| chr9:92525904 | A | G | 1 | a0002c0003t0001g0042 | 2 | NA18983.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-27-3011T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525904 | |||||||
| chr9:92525916 | G | A | 1 | a0010c0022t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-27-3023C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525916 | |||||||
| chr9:92525925 | A | T | 1 | a0001c0002t0005g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-27-3032T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92525925 | |||||||
| chr9:92526041 | C | A | 117 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(114): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-27-3148G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92526041 | |||||||
| chr9:92526055 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-27-3162C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92526055 | |||||||
| chr9:92526070 | G | A | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-27-3177C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92526070 | |||||||
| chr9:92526284 | C | T | 8 | a0001c0001t0001g0049 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
11 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-27-3391G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92526284 | |||||||
| chr9:92526514 | G | A | 8 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0122 others(5): Show |
14 | HG03579.hp2 NA18940.hp1 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27-3621C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92526514 | |||||||
| chr9:92527003 | A | ATTAT | 4 | a0001c0002t0002g0075 a0001c0002t0002g0084 a0001c0002t0002g0085 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-4114_-27-4111d others(6): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527003 | |||||||
| chr9:92527134 | G | C | 1 | a0001c0002t0002g0033 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-27-4241C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527134 | |||||||
| chr9:92527250 | A | T | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-27-4357T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527250 | |||||||
| chr9:92527259 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-27-4366G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527259 | |||||||
| chr9:92527492 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-27-4599G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527492 | |||||||
| chr9:92527618 | T | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
18 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.-27-4725A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527618 | |||||||
| chr9:92527658 | A | C | 117 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(114): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-27-4765T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527658 | |||||||
| chr9:92527736 | TATTGTGA others(34): Show |
T | 1 | a0001c0006t0001g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-27-4884_-27-4844d others(43): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527736 | |||||||
| chr9:92527749 | T | G | 1 | a0002c0003t0001g0002 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-27-4856A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527749 | |||||||
| chr9:92527949 | T | A | 1 | a0001c0002t0002g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-27-5056A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92527949 | |||||||
| chr9:92528138 | C | T | 5 | a0001c0002t0002g0034 a0001c0002t0002g0074 a0001c0002t0002g0113 others(2): Show |
6 | HG02145.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-5245G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528138 | |||||||
| chr9:92528139 | G | A | 1 | a0002c0003t0001g0186 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-27-5246C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528139 | |||||||
| chr9:92528174 | G | A | 115 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(112): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-27-5281C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528174 | |||||||
| chr9:92528241 | G | A | 1 | a0002c0003t0001g0187 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-27-5348C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528241 | |||||||
| chr9:92528372 | G | C | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-27-5479C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528372 | |||||||
| chr9:92528378 | CAA | C | 17 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(14): Show |
20 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27-5487_-27-5486d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528378 | |||||||
| chr9:92528547 | ACAAAG | A | 92 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(89): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-27-5659_-27-5655d others(7): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528547 | |||||||
| chr9:92528548 | C | G | 1 | a0001c0002t0002g0109 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-27-5655G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528548 | |||||||
| chr9:92528552 | G | A | 23 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0002g0109 others(20): Show |
26 | HG00280.hp1 HG00735.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-27-5659C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528552 | |||||||
| chr9:92528558 | CAAAACAA others(67): Show |
C | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-27-5739_-27-5666d others(76): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528558 | |||||||
| chr9:92528614 | CCACCAGT | C | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-5728_-27-5722d others(9): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528614 | |||||||
| chr9:92528694 | A | T | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-27-5801T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528694 | |||||||
| chr9:92528766 | AT | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-27-5874delA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528766 | |||||||
| chr9:92528848 | C | A | 3 | a0001c0002t0002g0017 a0001c0002t0002g0118 a0001c0002t0002g0119 |
5 | HG02145.hp1 HG02647.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-5955G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528848 | |||||||
| chr9:92528865 | T | C | 1 | a0002c0003t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-27-5972A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528865 | |||||||
| chr9:92528877 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-27-5984C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528877 | |||||||
| chr9:92528886 | C | A | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-27-5993G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92528886 | |||||||
| chr9:92529232 | A | T | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-27-6339T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529232 | |||||||
| chr9:92529358 | G | A | 1 | a0001c0002t0002g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-27-6465C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529358 | |||||||
| chr9:92529469 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-28+6464T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529469 | |||||||
| chr9:92529627 | A | G | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-28+6306T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529627 | |||||||
| chr9:92529775 | T | C | 1 | a0002c0003t0001g0190 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-28+6158A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529775 | |||||||
| chr9:92529797 | C | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+6136G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529797 | |||||||
| chr9:92529836 | G | T | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+6097C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529836 | |||||||
| chr9:92529883 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0047 others(14): Show |
41 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.-28+6050C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529883 | |||||||
| chr9:92529926 | A | G | 2 | a0002c0007t0001g0015 a0002c0007t0001g0232 |
5 | HG02615.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+6007T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529926 | |||||||
| chr9:92529981 | T | A | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+5952A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92529981 | |||||||
| chr9:92530135 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-28+5798C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530135 | |||||||
| chr9:92530173 | C | A | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+5760G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530173 | |||||||
| chr9:92530175 | A | G | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+5758T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530175 | |||||||
| chr9:92530212 | C | T | 1 | a0001c0002t0002g0030 | 2 | HG00099.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-28+5721G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530212 | |||||||
| chr9:92530268 | A | C | 5 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0154 others(2): Show |
8 | HG01255.hp2 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+5665T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530268 | |||||||
| chr9:92530525 | A | G | 1 | a0002c0003t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-28+5408T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530525 | |||||||
| chr9:92530623 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-28+5310C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530623 | |||||||
| chr9:92530634 | T | C | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+5299A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530634 | |||||||
| chr9:92530817 | G | A | 1 | a0003c0004t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-28+5116C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530817 | |||||||
| chr9:92530862 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-28+5071G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92530862 | |||||||
| chr9:92531114 | T | G | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+4819A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531114 | |||||||
| chr9:92531251 | T | G | 6 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(3): Show |
9 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+4682A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531251 | |||||||
| chr9:92531359 | C | G | 94 | a0001c0002t0001g0120 a0001c0002t0002g0008 a0001c0002t0002g0009 others(91): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-28+4574G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531359 | |||||||
| chr9:92531452 | C | T | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+4481G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531452 | |||||||
| chr9:92531920 | A | AT | 2 | a0002c0007t0001g0015 a0002c0007t0001g0232 |
5 | HG02615.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+4012dupA | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531920 | |||||||
| chr9:92531974 | C | G | 1 | a0002c0007t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-28+3959G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92531974 | |||||||
| chr9:92532000 | C | T | 1 | a0001c0002t0002g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-28+3933G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532000 | |||||||
| chr9:92532005 | TTTATTTA others(22): Show |
T | 1 | a0001c0002t0002g0123 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-28+3899_-28+3927d others(31): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532005 | |||||||
| chr9:92532015 | G | GTTT | 30 | a0001c0002t0002g0010 a0001c0002t0002g0029 a0001c0002t0002g0031 others(27): Show |
35 | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-28+3915_-28+3917d others(5): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTT | 11 | a0001c0002t0002g0033 a0001c0002t0002g0083 a0001c0002t0002g0095 others(8): Show |
11 | HG01109.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28+3914_-28+3917d others(6): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTT | 6 | a0001c0002t0002g0010 a0001c0002t0002g0030 a0001c0002t0002g0093 others(3): Show |
6 | HG01074.hp2 HG01433.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+3913_-28+3917d others(7): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(13): Show |
1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(3): Show |
9 | a0001c0002t0002g0008 a0001c0002t0002g0037 a0001c0002t0002g0125 others(6): Show |
11 | HG00140.hp2 HG00733.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28+3908_-28+3917d others(12): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(4): Show |
9 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0085 others(6): Show |
10 | HG00597.hp1 HG00642.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+3907_-28+3917d others(13): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(5): Show |
14 | a0001c0002t0002g0008 a0001c0002t0002g0011 a0001c0002t0002g0019 others(11): Show |
16 | HG01358.hp1 HG01952.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-28+3906_-28+3917d others(14): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(6): Show |
5 | a0001c0002t0002g0035 a0001c0002t0002g0038 a0001c0002t0002g0039 others(2): Show |
5 | HG00639.hp2 HG00673.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+3905_-28+3917d others(15): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(7): Show |
6 | a0001c0002t0002g0040 a0001c0002t0002g0084 a0001c0002t0002g0124 others(3): Show |
6 | HG01243.hp1 HG02886.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(8): Show |
1 | a0003c0004t0002g0065 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(17): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(9): Show |
1 | a0001c0002t0002g0019 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(18): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(10): Show |
4 | a0001c0002t0002g0009 a0001c0002t0002g0017 a0001c0002t0002g0119 others(1): Show |
5 | HG02647.hp2 HG03540.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(11): Show |
4 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0118 others(1): Show |
5 | HG02145.hp1 NA18940.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(12): Show |
2 | a0001c0002t0002g0020 a0001c0002t0002g0147 |
2 | NA18957.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(21): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(13): Show |
7 | a0001c0001t0001g0059 a0001c0002t0002g0017 a0001c0002t0002g0075 others(4): Show |
8 | HG00280.hp1 HG00735.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(14): Show |
1 | a0003c0004t0002g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(23): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(15): Show |
1 | a0001c0002t0002g0009 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(24): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(16): Show |
2 | a0001c0001t0001g0068 a0003c0004t0002g0066 |
2 | HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(25): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(18): Show |
1 | a0003c0004t0002g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(27): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(20): Show |
2 | a0003c0004t0002g0016 a0003c0004t0002g0063 |
2 | NA18951.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-28+3917_-28+3918i others(29): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(22): Show |
1 | a0001c0002t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(31): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532015 | G | GTTTTTTT others(23): Show |
1 | a0003c0004t0002g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-28+3917_-28+3918i others(32): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532015 | |||||||
| chr9:92532016 | T | TTTTTTTT others(4): Show |
4 | a0001c0002t0004g0134 a0001c0009t0002g0018 a0001c0009t0002g0139 others(1): Show |
6 | HG01081.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+3916_-28+3917i others(13): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532016 | |||||||
| chr9:92532020 | TTTTTTTT others(7): Show |
T | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-28+3899_-28+3912d others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532020 | |||||||
| chr9:92532025 | T | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(48): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-28+3908A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532025 | |||||||
| chr9:92532025 | T | C | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+3908A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532025 | |||||||
| chr9:92532028 | TA | T | 4 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0005t0001g0041 others(1): Show |
4 | HG02895.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+3904delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532028 | |||||||
| chr9:92532029 | A | T | 125 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(122): Show |
165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-28+3904T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532029 | |||||||
| chr9:92532033 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0024 others(5): Show |
9 | HG00609.hp2 HG02015.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+3900A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532033 | |||||||
| chr9:92532034 | A | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.-28+3899T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532034 | |||||||
| chr9:92532039 | T | A | 1 | a0002c0003t0001g0191 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-28+3894A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532039 | |||||||
| chr9:92532061 | A | G | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+3872T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532061 | |||||||
| chr9:92532264 | G | T | 1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+3669C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532264 | |||||||
| chr9:92532304 | T | TCACTCTG others(31): Show |
1 | a0001c0002t0002g0149 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-28+3591_-28+3628d others(40): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532304 | |||||||
| chr9:92532519 | G | A | 1 | a0001c0002t0002g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-28+3414C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532519 | |||||||
| chr9:92532532 | G | A | 3 | a0001c0002t0002g0017 a0001c0002t0002g0118 a0001c0002t0002g0119 |
5 | HG02145.hp1 HG02647.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+3401C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532532 | |||||||
| chr9:92532587 | T | C | 5 | a0001c0002t0002g0034 a0001c0002t0002g0074 a0001c0002t0002g0113 others(2): Show |
6 | HG02145.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+3346A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532587 | |||||||
| chr9:92532694 | T | G | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+3239A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532694 | |||||||
| chr9:92532829 | T | C | 1 | a0002c0003t0001g0192 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-28+3104A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92532829 | |||||||
| chr9:92533073 | C | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+2860G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533073 | |||||||
| chr9:92533074 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-28+2859C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533074 | |||||||
| chr9:92533142 | C | CA | 4 | a0001c0001t0001g0049 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
5 | HG00099.hp1 HG00140.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+2790dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533142 | |||||||
| chr9:92533171 | G | A | 1 | a0001c0002t0002g0150 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-28+2762C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533171 | |||||||
| chr9:92533173 | G | A | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-28+2760C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533173 | |||||||
| chr9:92533197 | A | G | 123 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(120): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-28+2736T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533197 | |||||||
| chr9:92533210 | G | T | 2 | a0002c0003t0001g0157 a0002c0003t0001g0158 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-28+2723C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533210 | |||||||
| chr9:92533225 | G | A | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-28+2708C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533225 | |||||||
| chr9:92533228 | A | AG | 6 | a0001c0002t0002g0029 a0001c0002t0002g0078 a0001c0002t0002g0079 others(3): Show |
7 | HG00323.hp2 HG00733.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+2704dupC | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533228 | |||||||
| chr9:92533269 | C | A | 2 | a0001c0002t0002g0116 a0001c0002t0002g0117 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28+2664G>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533269 | |||||||
| chr9:92533298 | T | TCAAA | 6 | a0001c0001t0001g0068 a0003c0004t0002g0016 a0003c0004t0002g0056 others(3): Show |
8 | HG00280.hp1 HG02015.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+2631_-28+2634d others(6): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533298 | |||||||
| chr9:92533303 | C | CA | 5 | a0002c0003t0001g0002 a0002c0003t0001g0005 a0002c0003t0001g0007 others(2): Show |
11 | HG00639.hp1 HG01361.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28+2629dupT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533303 | |||||||
| chr9:92533303 | CA | C | 20 | a0001c0002t0002g0008 a0001c0002t0002g0010 a0001c0002t0002g0037 others(17): Show |
22 | HG00140.hp2 HG01070.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28+2629delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533303 | |||||||
| chr9:92533303 | CAA | C | 7 | a0001c0002t0002g0008 a0001c0002t0002g0031 a0001c0002t0002g0105 others(4): Show |
7 | HG00733.hp2 HG01515.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+2628_-28+2629d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533303 | |||||||
| chr9:92533303 | CAAA | C | 19 | a0001c0002t0001g0120 a0001c0002t0002g0010 a0001c0002t0002g0030 others(16): Show |
23 | HG00099.hp2 HG00642.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-28+2627_-28+2629d others(5): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533303 | |||||||
| chr9:92533303 | CAAAAA | C | 5 | a0001c0002t0002g0040 a0001c0006t0001g0027 a0001c0006t0001g0071 others(2): Show |
8 | HG00639.hp2 HG02698.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+2625_-28+2629d others(7): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533303 | |||||||
| chr9:92533307 | A | C | 7 | a0001c0002t0002g0078 a0001c0002t0002g0079 a0003c0004t0002g0055 others(4): Show |
7 | HG00733.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+2626T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533307 | |||||||
| chr9:92533311 | A | C | 1 | a0001c0006t0001g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-28+2622T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533311 | |||||||
| chr9:92533312 | A | AATATATA others(7): Show |
1 | a0001c0005t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28+2620_-28+2621i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533312 | |||||||
| chr9:92533312 | A | T | 1 | a0001c0005t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-28+2621T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533312 | |||||||
| chr9:92533314 | A | AATATATA others(7): Show |
1 | a0001c0005t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+2618_-28+2619i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533314 | |||||||
| chr9:92533314 | A | C | 1 | a0001c0006t0001g0071 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-28+2619T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533314 | |||||||
| chr9:92533314 | A | T | 3 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0154 |
6 | HG01255.hp2 HG02257.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+2619T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533314 | |||||||
| chr9:92533315 | AAAAAAAA others(18): Show |
A | 1 | a0001c0005t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-28+2593_-28+2617d others(27): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533315 | |||||||
| chr9:92533316 | A | T | 4 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0154 others(1): Show |
7 | HG01255.hp2 HG02257.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+2617T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533316 | |||||||
| chr9:92533317 | AAAAAAAA others(6): Show |
A | 4 | a0001c0002t0002g0029 a0001c0002t0002g0079 a0001c0002t0002g0080 others(1): Show |
5 | HG00323.hp2 HG01257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+2603_-28+2615d others(15): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533317 | |||||||
| chr9:92533318 | A | AT | 3 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0148 |
3 | NA19003.hp1 NA19011.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-28+2614_-28+2615i others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533318 | |||||||
| chr9:92533318 | A | T | 5 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0154 others(2): Show |
8 | HG01255.hp2 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+2615T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533318 | |||||||
| chr9:92533319 | AAAAAAAA others(6): Show |
A | 2 | a0001c0002t0002g0078 a0001c0002t0002g0082 |
2 | HG00733.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-28+2601_-28+2613d others(15): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533319 | |||||||
| chr9:92533320 | A | AATATATA others(11): Show |
1 | a0001c0002t0002g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-28+2612_-28+2613i others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533320 | |||||||
| chr9:92533320 | A | AT | 6 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0122 others(3): Show |
7 | HG03540.hp1 NA18951.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+2612_-28+2613i others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533320 | |||||||
| chr9:92533320 | A | T | 8 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0148 others(5): Show |
12 | HG01255.hp2 HG02257.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-28+2613T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533320 | |||||||
| chr9:92533322 | A | ATATATAT | 3 | a0001c0002t0002g0017 a0001c0002t0002g0039 a0001c0002t0002g0133 |
4 | HG03471.hp1 NA18955.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+2610_-28+2611i others(9): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533322 | |||||||
| chr9:92533322 | A | ATATATAT others(8): Show |
1 | a0001c0002t0002g0008 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-28+2610_-28+2611i others(17): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533322 | |||||||
| chr9:92533322 | A | ATATATAT others(10): Show |
2 | a0001c0002t0002g0038 a0001c0002t0002g0149 |
2 | NA18950.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-28+2610_-28+2611i others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533322 | |||||||
| chr9:92533322 | A | T | 17 | a0001c0002t0002g0009 a0001c0002t0002g0020 a0001c0002t0002g0038 others(14): Show |
25 | HG00642.hp1 HG00673.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+2611T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533322 | |||||||
| chr9:92533324 | A | AT | 7 | a0001c0002t0002g0011 a0001c0002t0002g0019 a0001c0002t0002g0123 others(4): Show |
7 | NA18947.hp2 NA18960.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+2608_-28+2609i others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533324 | |||||||
| chr9:92533324 | A | ATATATAT others(4): Show |
1 | a0001c0002t0002g0118 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-28+2608_-28+2609i others(13): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533324 | |||||||
| chr9:92533324 | A | T | 29 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(26): Show |
45 | HG00642.hp1 HG00673.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+2609T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533324 | |||||||
| chr9:92533326 | A | AT | 4 | a0001c0002t0002g0011 a0001c0002t0002g0087 a0001c0011t0001g0032 others(1): Show |
6 | HG00280.hp2 HG01168.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+2606_-28+2607i others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533326 | |||||||
| chr9:92533326 | A | T | 52 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(49): Show |
75 | HG00597.hp1 HG00642.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.-28+2607T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533326 | |||||||
| chr9:92533328 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0006 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(21): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0004 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(18): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0006 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0004 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0004 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(24): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(10): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0221 |
2 | HG02071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0212 |
2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(23): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0003 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0210 a0001c0001t0001g0214 |
2 | HG03017.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(18): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0006 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0049 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(44): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAT others(8): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0047 |
3 | HG00597.hp2 HG02523.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(17): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0001g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(23): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(3): Show |
1 | a0001c0001t0001g0006 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(12): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(14): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(7): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0222 |
4 | HG02129.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(11): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0220 |
4 | HG00408.hp2 HG01069.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(13): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0048 others(1): Show |
5 | HG00423.hp2 HG00558.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(22): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(17): Show |
2 | a0001c0001t0001g0003 a0002c0007t0001g0232 |
2 | HG02615.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(26): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAAATA others(25): Show |
1 | a0001c0001t0001g0049 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(34): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(4): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0224 |
2 | HG02027.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(13): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0213 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0003 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(17): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0004 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(12): Show |
1 | a0001c0001t0001g0004 | 2 | NA18944.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(21): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(18): Show |
1 | a0002c0007t0001g0015 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(27): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAAATAT others(54): Show |
1 | a0001c0001t0001g0229 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(63): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(16): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAATATA others(9): Show |
1 | a0002c0007t0001g0015 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(18): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0004 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAATATA others(17): Show |
1 | a0002c0007t0001g0015 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(26): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAAATATA others(25): Show |
1 | a0001c0001t0001g0228 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-28+2604_-28+2605i others(34): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AAT | 6 | a0001c0002t0002g0008 a0002c0003t0001g0002 a0002c0003t0001g0042 others(3): Show |
9 | HG00438.hp2 HG01169.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+2603_-28+2604d others(4): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0004 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-28+2595_-28+2604d others(12): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AATATATA others(17): Show |
1 | a0002c0007t0001g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+2581_-28+2604d others(26): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | AT | 5 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0002t0002g0110 others(2): Show |
5 | HG01167.hp1 HG01255.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+2604_-28+2605i others(3): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | A | T | 80 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0010 others(77): Show |
113 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.-28+2605T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | AATATATA others(1): Show |
A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(22): Show |
59 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-28+2597_-28+2604d others(10): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0014 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-28+2595_-28+2604d others(12): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533328 | AATATATA others(11): Show |
A | 1 | a0008c0025t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-28+2587_-28+2604d others(20): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533328 | |||||||
| chr9:92533329 | ATATATAT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
10 | HG00408.hp1 HG02027.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+2597_-28+2603d others(9): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533329 | |||||||
| chr9:92533329 | ATATATAT others(2): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0204 others(1): Show |
6 | HG01256.hp2 NA18946.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+2595_-28+2603d others(11): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533329 | |||||||
| chr9:92533330 | T | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0068 others(32): Show |
46 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.-28+2603A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533330 | |||||||
| chr9:92533332 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0002c0003t0001g0002 others(11): Show |
17 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28+2601A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533332 | |||||||
| chr9:92533334 | T | A | 6 | a0001c0001t0001g0006 a0002c0003t0001g0177 a0002c0003t0001g0189 others(3): Show |
6 | HG00642.hp2 HG01261.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+2599A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533334 | |||||||
| chr9:92533336 | T | A | 4 | a0001c0001t0001g0006 a0001c0002t0002g0104 a0004c0015t0003g0076 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+2597A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533336 | |||||||
| chr9:92533338 | T | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(24): Show |
63 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-28+2595A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533338 | |||||||
| chr9:92533340 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0200 others(2): Show |
10 | HG01243.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+2593A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533340 | |||||||
| chr9:92533342 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-28+2591A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533342 | |||||||
| chr9:92533344 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-28+2589A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533344 | |||||||
| chr9:92533346 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-28+2587A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533346 | |||||||
| chr9:92533348 | T | A | 2 | a0001c0001t0001g0230 a0008c0025t0001g0121 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-28+2585A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533348 | |||||||
| chr9:92533350 | T | A | 1 | a0008c0025t0001g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-28+2583A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533350 | |||||||
| chr9:92533353 | A | G | 1 | a0001c0002t0002g0122 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-28+2580T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533353 | |||||||
| chr9:92533358 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0231 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-28+2574_-28+2575i others(28): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533358 | |||||||
| chr9:92533443 | C | T | 2 | a0004c0015t0003g0076 a0004c0015t0003g0077 |
2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-28+2490G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533443 | |||||||
| chr9:92533776 | G | A | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(42): Show |
70 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.-28+2157C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533776 | |||||||
| chr9:92533853 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.-28+2080G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533853 | |||||||
| chr9:92533986 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-28+1947A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92533986 | |||||||
| chr9:92534157 | G | C | 1 | a0001c0002t0002g0151 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-28+1776C>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534157 | |||||||
| chr9:92534357 | C | T | 6 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(3): Show |
9 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+1576G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534357 | |||||||
| chr9:92534358 | T | G | 9 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0005t0001g0021 others(6): Show |
12 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-28+1575A>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534358 | |||||||
| chr9:92534389 | A | G | 6 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0050 others(3): Show |
9 | HG01081.hp1 HG01255.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+1544T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534389 | |||||||
| chr9:92534474 | G | A | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+1459C>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534474 | |||||||
| chr9:92534491 | G | T | 1 | a0001c0002t0002g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-28+1442C>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534491 | |||||||
| chr9:92534559 | A | AACTTTTT others(27): Show |
1 | a0002c0003t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-28+1340_-28+1373d others(36): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534559 | |||||||
| chr9:92534620 | A | C | 1 | a0002c0003t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-28+1313T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534620 | |||||||
| chr9:92534795 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-28+1138A>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534795 | |||||||
| chr9:92534823 | C | T | 5 | a0001c0005t0001g0021 a0001c0005t0001g0041 a0001c0005t0001g0154 others(2): Show |
8 | HG01255.hp2 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+1110G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534823 | |||||||
| chr9:92534828 | A | G | 1 | a0002c0003t0001g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-28+1105T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92534828 | |||||||
| chr9:92535054 | C | G | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+879G>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535054 | |||||||
| chr9:92535086 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-28+847G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535086 | |||||||
| chr9:92535132 | G | GTA | 42 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(39): Show |
65 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-28+800_-28+801ins others(2): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535132 | |||||||
| chr9:92535136 | T | TAGATACT others(12): Show |
42 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0011 others(39): Show |
65 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.-28+796_-28+797ins others(19): Show |
ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535136 | |||||||
| chr9:92535309 | C | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+624G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535309 | |||||||
| chr9:92535319 | A | C | 1 | a0001c0002t0002g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-28+614T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535319 | |||||||
| chr9:92535497 | T | A | 1 | a0002c0003t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-28+436A>T | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535497 | |||||||
| chr9:92535563 | A | G | 5 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0071 others(2): Show |
7 | HG00642.hp1 HG01358.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+370T>C | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535563 | |||||||
| chr9:92535589 | A | C | 124 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0002t0001g0120 others(121): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-28+344T>G | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535589 | |||||||
| chr9:92535655 | TA | T | 21 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0003c0004t0002g0016 others(18): Show |
24 | HG00280.hp1 HG00735.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-28+277delT | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535655 | |||||||
| chr9:92535714 | A | T | 1 | a0002c0003t0001g0051 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-28+219T>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535714 | |||||||
| chr9:92535810 | C | T | 1 | a0001c0005t0001g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-28+123G>A | ECM2 | ENSG00000106823.13 | transcript | ENST00000344604.10 | protein_coding | 1/9 | chr9 | 92535810 |