Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11316 |
| ensemblid | ENSG00000105669.14 |
| hgncid | 2234 |
| symbol | COPE |
| name | COPI coat complex subunit epsilon |
| refseq_nuc | NM_007263.4 |
| refseq_prot | NP_009194.2 |
| ensembl_nuc | ENST00000262812.9 |
| ensembl_prot | ENSP00000262812.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 18899514 |
| end | 18919387 |
| strand | - |
| ver | v1.2 |
| region | chr19:18899514-18919387 |
| region5000 | chr19:18894514-18924387 |
| regionname0 | COPE_chr19_18899514_18919387 |
| regionname5000 | COPE_chr19_18894514_18924387 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 308 | 215 | 19 | 44 | 103 | 13 | 34 | 73 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0002 | 0/0 | 308 | 75 | 36 | 11 | 17 | 1 | 10 | 15 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0003 | 0/0 | 308 | 33 | 33 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0004 | 0/0 | 308 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0005 | 0/0 | 308 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0006 | 0/0 | 308 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| a0007 | 0/0 | 308 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | MAPPA others(303): Show |
chr19 | 18894514 | 18924387 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 924 | 116 | 12 | 17 | 61 | 6 | 19 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0001c0002 | 0/1 | 924 | 93 | 6 | 26 | 39 | 7 | 14 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0001c0009 | 0/0 | 924 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0001c0010 | 0/0 | 924 | 2 | 1 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0001c0012 | 0/0 | 924 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0002c0003 | 0/0 | 924 | 72 | 36 | 11 | 14 | 1 | 10 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0002c0007 | 0/0 | 924 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0004 | 0/0 | 924 | 17 | 17 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0005 | 0/0 | 924 | 7 | 7 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0008 | 0/0 | 924 | 3 | 3 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0011 | 0/0 | 924 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0016 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0017 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0018 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0003c0019 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0004c0006 | 0/0 | 924 | 4 | 4 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0005c0014 | 0/0 | 924 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0006c0013 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 | ||
| a0007c0015 | 0/0 | 924 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | ATGGC others(919): Show |
chr19 | 18894514 | 18924387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1131 | 116 | 12 | 17 | 61 | 6 | 19 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0001c0002t0001 | 0/1 | 1131 | 93 | 6 | 26 | 39 | 7 | 14 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0001c0009t0001 | 0/0 | 1131 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0001c0010t0001 | 0/0 | 1131 | 2 | 1 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0001c0012t0001 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0002c0003t0001 | 0/0 | 1131 | 72 | 36 | 11 | 14 | 1 | 10 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0002c0007t0001 | 0/0 | 1131 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0004t0001 | 0/0 | 1131 | 17 | 17 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0005t0001 | 0/0 | 1131 | 7 | 7 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0008t0001 | 0/0 | 1131 | 3 | 3 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0011t0001 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0016t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0017t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0018t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0003c0019t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0004c0006t0001 | 0/0 | 1131 | 4 | 4 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0005c0014t0001 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0006c0013t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| a0007c0015t0001 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | GTGTC others(1126): Show |
chr19 | 18894514 | 18924387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0002 | 1/0 | 6 | 0 | 1 | 4 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0002t0001g0261 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0009t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0009t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0009t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0010t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0010t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0001c0012t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0003t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0007t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0002c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0008t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0008t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0011t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0011t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0016t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0017t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0018t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0003c0019t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0004c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0004c0006t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0004c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0004c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0005c0014t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0006c0013t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| a0007c0015t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0136 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0223 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0221 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0100 | EUR | FIN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00609 | hp1 | a0002 | c0007 | t0001 | g0135 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00738 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01070 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0129 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01109 | hp2 | a0002 | c0003 | t0001 | g0192 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0113 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0137 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0169 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0045 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0147 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01496 | hp2 | a0001 | c0010 | t0001 | g0036 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0244 | EUR | IBS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0291 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0126 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01928 | hp2 | a0005 | c0014 | t0001 | g0097 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02055 | hp1 | a0003 | c0008 | t0001 | g0277 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02055 | hp2 | a0003 | c0005 | t0001 | g0274 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0253 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02145 | hp2 | a0003 | c0005 | t0001 | g0272 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | CDX | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0121 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0148 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0287 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0154 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02280 | hp1 | a0004 | c0006 | t0001 | g0038 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0157 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0193 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0266 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02572 | hp1 | a0003 | c0011 | t0001 | g0275 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02572 | hp2 | a0007 | c0015 | t0001 | g0292 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0138 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0144 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0204 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0203 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02630 | hp1 | a0003 | c0017 | t0001 | g0283 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0042 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0127 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0125 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02723 | hp1 | a0003 | c0005 | t0001 | g0271 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0040 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0146 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0152 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0202 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0259 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0018 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0248 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0019 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0019 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0145 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0130 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0280 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0159 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0143 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02970 | hp2 | a0003 | c0016 | t0001 | g0276 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0254 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03041 | hp1 | a0003 | c0004 | t0001 | g0284 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03041 | hp2 | a0003 | c0019 | t0001 | g0286 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03098 | hp1 | a0003 | c0004 | t0001 | g0285 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0200 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03130 | hp1 | a0003 | c0005 | t0001 | g0268 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0201 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0194 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03195 | hp2 | a0003 | c0018 | t0001 | g0282 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0188 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0273 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0289 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03453 | hp1 | a0004 | c0006 | t0001 | g0122 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0196 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0191 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03516 | hp1 | a0003 | c0008 | t0001 | g0279 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0155 | AFR | ESN | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0290 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0263 | AFR | GWD | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03579 | hp1 | a0004 | c0006 | t0001 | g0142 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0264 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0120 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0039 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0041 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03927 | hp2 | a0002 | c0003 | t0001 | g0153 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0251 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04115 | hp2 | a0002 | c0003 | t0001 | g0123 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04184 | hp1 | a0001 | c0012 | t0001 | g0028 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0198 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0210 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | STU | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0195 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18522 | hp2 | a0003 | c0005 | t0001 | g0269 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18612 | hp2 | a0001 | c0009 | t0001 | g0295 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0249 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18959 | hp1 | a0002 | c0007 | t0001 | g0140 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19004 | hp2 | a0002 | c0007 | t0001 | g0134 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19043 | hp2 | a0003 | c0004 | t0001 | g0265 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19057 | hp2 | a0001 | c0009 | t0001 | g0294 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19068 | hp2 | a0001 | c0009 | t0001 | g0293 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19074 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0281 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0288 | AFR | YRI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ASW | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ASW | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | GIH | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0270 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0252 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02486 | hp2 | a0006 | c0013 | t0001 | g0250 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02559 | hp1 | a0003 | c0011 | t0001 | g0267 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG02559 | hp2 | a0003 | c0008 | t0001 | g0278 | AFR | ACB | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0197 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0189 | AFR | MSL | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0158 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA20300 | hp2 | a0001 | c0010 | t0001 | g0141 | AFR | USA | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA21309 | hp1 | a0004 | c0006 | t0001 | g0114 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0261 | REF | REF | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | COPE_chr19_18894514_18924387 | COPE | chr19 | 18894514 | 18924387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18899880 | T | C | 1 | a0005 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.872A>G | p.Gln291Arg | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 9/10 | 911/1131 | 872/927 | 291/308 | chr19 | 18899880 | |||
| chr19:18899893 | T | G | 1 | a0005 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.859A>C | p.Ile287Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 9/10 | 898/1131 | 859/927 | 287/308 | chr19 | 18899893 | |||
| chr19:18907024 | A | G | 1 | a0006 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.379T>C | p.Tyr127His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 418/1131 | 379/927 | 127/308 | chr19 | 18907024 | |||
| chr19:18907053 | G | A | 3 | a0002 a0006 a0007 |
77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 389/1131 | 350/927 | 117/308 | chr19 | 18907053 | |||
| chr19:18911007 | C | T | 1 | a0004 | 4 | HG02280.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.254G>A | p.Arg85His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/10 | 293/1131 | 254/927 | 85/308 | chr19 | 18911007 | |||
| chr19:18919311 | G | C | 2 | a0003 a0007 |
34 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(31): Show |
missense_variant | MODERATE | c.38C>G | p.Ser13Cys | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/10 | 77/1131 | 38/927 | 13/308 | chr19 | 18919311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18900435 | T | C | 9 | a0001c0002 a0001c0010 a0003c0004 others(6): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
synonymous_variant | LOW | c.750A>G | p.Pro250Pro | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/10 | 789/1131 | 750/927 | 250/308 | chr19 | 18900435 | |||
| chr19:18904798 | G | A | 1 | a0002c0007 | 3 | HG00609.hp1 NA18959.hp1 NA19004.hp2 |
synonymous_variant | LOW | c.552C>T | p.Leu184Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/10 | 591/1131 | 552/927 | 184/308 | chr19 | 18904798 | |||
| chr19:18906968 | G | A | 1 | a0003c0019 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.435C>T | p.Ser145Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 474/1131 | 435/927 | 145/308 | chr19 | 18906968 | |||
| chr19:18906986 | C | T | 1 | a0003c0017 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.417G>A | p.Ala139Ala | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 456/1131 | 417/927 | 139/308 | chr19 | 18906986 | |||
| chr19:18907016 | G | A | 1 | a0001c0012 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.387C>T | p.His129His | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 426/1131 | 387/927 | 129/308 | chr19 | 18907016 | |||
| chr19:18907019 | G | T | 1 | a0006c0013 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.384C>A | p.Leu128Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/10 | 423/1131 | 384/927 | 128/308 | chr19 | 18907019 | |||
| chr19:18911033 | G | A | 2 | a0003c0008 a0003c0016 |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.228C>T | p.Ser76Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/10 | 267/1131 | 228/927 | 76/308 | chr19 | 18911033 | |||
| chr19:18912987 | C | T | 1 | a0003c0016 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.186G>A | p.Ala62Ala | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/10 | 225/1131 | 186/927 | 62/308 | chr19 | 18912987 | |||
| chr19:18913044 | T | C | 8 | a0001c0002 a0003c0004 a0003c0008 others(5): Show |
117 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(114): Show |
splice_region_variant&synonymous_variant | LOW | c.129A>G | p.Leu43Leu | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/10 | 168/1131 | 129/927 | 43/308 | chr19 | 18913044 | |||
| chr19:18919319 | G | A | 1 | a0001c0009 | 3 | NA18612.hp2 NA19057.hp2 NA19068.hp2 |
synonymous_variant | LOW | c.30C>T | p.Ser10Ser | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/10 | 69/1131 | 30/927 | 10/308 | chr19 | 18919319 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18900094 | C | G | 3 | a0002c0007t0001g0134 a0002c0007t0001g0135 a0002c0007t0001g0140 |
3 | HG00609.hp1 NA18959.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.805-147G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900094 | |||||||
| chr19:18900104 | G | C | 20 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(17): Show |
21 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.805-157C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900104 | |||||||
| chr19:18900117 | TG | T | 3 | a0001c0001t0001g0084 a0001c0002t0001g0176 a0005c0014t0001g0097 |
3 | HG01928.hp2 HG03491.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.805-171delC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900117 | |||||||
| chr19:18900124 | GC | G | 90 | a0001c0001t0001g0084 a0001c0001t0001g0112 a0001c0001t0001g0115 others(87): Show |
93 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.805-178delG | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900124 | |||||||
| chr19:18900139 | G | A | 22 | a0002c0003t0001g0113 a0002c0003t0001g0137 a0002c0003t0001g0188 others(19): Show |
22 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.805-192C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900139 | |||||||
| chr19:18900164 | ATGGTGGG others(10): Show |
A | 1 | a0002c0003t0001g0193 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.804+200_804+216del others(17): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 8/9 | chr19 | 18900164 | |||||||
| chr19:18900575 | G | A | 7 | a0003c0004t0001g0018 a0003c0004t0001g0263 a0003c0004t0001g0281 others(4): Show |
8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-126C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900575 | |||||||
| chr19:18900706 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.736-257A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900706 | |||||||
| chr19:18900965 | G | C | 204 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(201): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.736-516C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900965 | |||||||
| chr19:18900970 | T | C | 13 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(10): Show |
14 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.736-521A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900970 | |||||||
| chr19:18900983 | C | T | 1 | a0001c0009t0001g0293 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.736-534G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18900983 | |||||||
| chr19:18901056 | T | C | 75 | a0002c0003t0001g0005 a0002c0003t0001g0016 a0002c0003t0001g0039 others(72): Show |
78 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.736-607A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901056 | |||||||
| chr19:18901076 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.736-627G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901076 | |||||||
| chr19:18901117 | GGGGGACC others(9): Show |
G | 1 | a0002c0003t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.736-684_736-669del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901117 | |||||||
| chr19:18901250 | T | C | 6 | a0002c0003t0001g0113 a0002c0003t0001g0137 a0002c0003t0001g0202 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.736-801A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901250 | |||||||
| chr19:18901413 | C | T | 7 | a0003c0004t0001g0018 a0003c0004t0001g0263 a0003c0004t0001g0281 others(4): Show |
8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.736-964G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901413 | |||||||
| chr19:18901444 | A | G | 4 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0004t0001g0288 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-995T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901444 | |||||||
| chr19:18901498 | AGCAGTAC others(3): Show |
A | 1 | a0001c0002t0001g0218 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.736-1059_736-1050d others(12): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901498 | |||||||
| chr19:18901549 | G | A | 85 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(82): Show |
88 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(85): Show |
intron_variant | MODIFIER | c.736-1100C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901549 | |||||||
| chr19:18901682 | A | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0164 others(1): Show |
5 | HG00140.hp2 HG01981.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-1233T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901682 | |||||||
| chr19:18901796 | G | A | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901796 | |||||||
| chr19:18901806 | G | A | 2 | a0001c0002t0001g0180 a0001c0002t0001g0235 |
2 | NA19009.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.736-1357C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901806 | |||||||
| chr19:18901841 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.736-1392C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901841 | |||||||
| chr19:18901906 | C | T | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1362G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18901906 | |||||||
| chr19:18902179 | C | CA | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
42 | HG00597.hp2 HG00673.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.735+1088dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | |||||||
| chr19:18902179 | C | CAA | 73 | a0001c0001t0001g0054 a0001c0001t0001g0112 a0001c0001t0001g0115 others(70): Show |
76 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.735+1087_735+1088d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | |||||||
| chr19:18902179 | C | CAAA | 13 | a0002c0003t0001g0043 a0002c0003t0001g0079 a0002c0003t0001g0094 others(10): Show |
13 | HG00609.hp1 HG01175.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.735+1086_735+1088d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | |||||||
| chr19:18902179 | CA | C | 74 | a0001c0001t0001g0069 a0001c0002t0001g0031 a0001c0002t0001g0032 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.735+1088delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | |||||||
| chr19:18902179 | CAAAA | C | 20 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 others(17): Show |
21 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+1085_735+1088d others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902179 | |||||||
| chr19:18902282 | G | A | 7 | a0003c0004t0001g0018 a0003c0004t0001g0263 a0003c0004t0001g0281 others(4): Show |
8 | HG02258.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.735+986C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902282 | |||||||
| chr19:18902324 | C | T | 1 | a0002c0003t0001g0131 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.735+944G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902324 | |||||||
| chr19:18902391 | G | A | 1 | a0003c0004t0001g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+877C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902391 | |||||||
| chr19:18902607 | T | G | 21 | a0003c0004t0001g0018 a0003c0004t0001g0019 a0003c0004t0001g0263 others(18): Show |
23 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.735+661A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902607 | |||||||
| chr19:18902664 | CA | C | 185 | a0001c0001t0001g0034 a0001c0001t0001g0066 a0001c0001t0001g0084 others(182): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.735+603delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902664 | |||||||
| chr19:18902707 | AAAGGAAG others(11): Show |
A | 1 | a0001c0002t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.735+543_735+560del others(18): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902707 | |||||||
| chr19:18902714 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.735+554C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902714 | |||||||
| chr19:18902716 | A | AAAGG | 56 | a0001c0002t0001g0168 a0001c0002t0001g0175 a0001c0002t0001g0181 others(53): Show |
58 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.735+548_735+551dup others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | |||||||
| chr19:18902716 | A | AAAGGAAG others(6): Show |
37 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(34): Show |
37 | HG00642.hp1 HG00741.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.735+551_735+552ins others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | |||||||
| chr19:18902716 | A | AAAGGAAG others(24): Show |
1 | a0001c0002t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735+551_735+552ins others(31): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | |||||||
| chr19:18902716 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.735+552T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | |||||||
| chr19:18902716 | AAAGGAAA others(2): Show |
A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
23 | HG00597.hp2 HG00673.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.735+543_735+551del others(9): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902716 | |||||||
| chr19:18902720 | GA | G | 73 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(70): Show |
74 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(71): Show |
intron_variant | MODIFIER | c.735+547delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902720 | |||||||
| chr19:18902721 | A | AAGGAAAG others(10): Show |
2 | a0003c0011t0001g0267 a0003c0011t0001g0275 |
2 | HG02559.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.735+546_735+547ins others(17): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902721 | |||||||
| chr19:18902723 | A | G | 7 | a0002c0003t0001g0005 a0002c0003t0001g0039 a0002c0003t0001g0040 others(4): Show |
9 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+545T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902723 | |||||||
| chr19:18902723 | A | T | 1 | a0002c0003t0001g0150 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.735+545T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902723 | |||||||
| chr19:18902725 | G | A | 7 | a0002c0003t0001g0005 a0002c0003t0001g0039 a0002c0003t0001g0040 others(4): Show |
9 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+543C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902725 | |||||||
| chr19:18902728 | G | A | 61 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(58): Show |
62 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.735+540C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902728 | |||||||
| chr19:18902728 | G | GGAA | 6 | a0002c0003t0001g0005 a0002c0003t0001g0039 a0002c0003t0001g0040 others(3): Show |
8 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+537_735+539dup others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902728 | |||||||
| chr19:18902730 | A | AAGG | 13 | a0002c0003t0001g0043 a0002c0003t0001g0126 a0003c0004t0001g0019 others(10): Show |
14 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.735+537_735+538ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902730 | |||||||
| chr19:18902730 | A | G | 61 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(58): Show |
62 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.735+538T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902730 | |||||||
| chr19:18902738 | GA | G | 19 | a0001c0001t0001g0112 a0001c0010t0001g0141 a0002c0003t0001g0005 others(16): Show |
21 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.735+529delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902738 | |||||||
| chr19:18902741 | A | G | 1 | a0002c0003t0001g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+527T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902741 | |||||||
| chr19:18902743 | G | A | 1 | a0002c0003t0001g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+525C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902743 | |||||||
| chr19:18902747 | GA | G | 33 | a0001c0001t0001g0112 a0001c0010t0001g0141 a0002c0003t0001g0005 others(30): Show |
37 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.735+520delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902747 | |||||||
| chr19:18902748 | A | AAGG | 53 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(50): Show |
53 | HG00609.hp1 HG01109.hp2 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.735+519_735+520ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902748 | |||||||
| chr19:18902752 | G | A | 2 | a0002c0003t0001g0043 a0002c0003t0001g0126 |
2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.735+516C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902752 | |||||||
| chr19:18902752 | G | GAAGGA | 20 | a0001c0002t0001g0168 a0001c0002t0001g0205 a0001c0002t0001g0206 others(17): Show |
20 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.735+511_735+515dup others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902752 | |||||||
| chr19:18902756 | G | GA | 12 | a0001c0002t0001g0014 a0001c0002t0001g0099 a0001c0002t0001g0106 others(9): Show |
13 | HG01167.hp1 HG01175.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.735+511dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | |||||||
| chr19:18902756 | G | GAAAGGAA others(3): Show |
1 | a0001c0002t0001g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.735+511_735+512ins others(10): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | |||||||
| chr19:18902756 | G | GAAAGGAA others(21): Show |
7 | a0001c0002t0001g0044 a0001c0002t0001g0100 a0001c0002t0001g0101 others(4): Show |
7 | HG00099.hp2 HG00323.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+511_735+512ins others(28): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902756 | |||||||
| chr19:18902757 | AAGG | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 others(4): Show |
7 | HG00323.hp1 HG02451.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+508_735+510del others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902757 | |||||||
| chr19:18902757 | AAGGAAGG others(9): Show |
A | 1 | a0001c0002t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.735+495_735+510del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902757 | |||||||
| chr19:18902760 | G | A | 2 | a0002c0003t0001g0043 a0002c0003t0001g0126 |
2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.735+508C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902760 | |||||||
| chr19:18902763 | G | A | 5 | a0001c0002t0001g0219 a0002c0003t0001g0129 a0002c0003t0001g0136 others(2): Show |
5 | HG00099.hp1 HG01081.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+505C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902763 | |||||||
| chr19:18902765 | A | G | 1 | a0001c0002t0001g0219 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735+503T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902765 | |||||||
| chr19:18902767 | G | A | 90 | a0001c0001t0001g0112 a0001c0002t0001g0014 a0001c0002t0001g0031 others(87): Show |
94 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.735+501C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | |||||||
| chr19:18902767 | G | GGAA | 4 | a0003c0004t0001g0265 a0003c0011t0001g0267 a0003c0011t0001g0275 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+500_735+501ins others(3): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | |||||||
| chr19:18902767 | G | GGAAAGAA others(86): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0004c0006t0001g0114 |
3 | HG01123.hp2 HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.735+500_735+501ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | |||||||
| chr19:18902767 | G | GGAAAGAA others(86): Show |
1 | a0001c0001t0001g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.735+500_735+501ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | |||||||
| chr19:18902767 | G | GGAAGGAA others(90): Show |
1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.735+500_735+501ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902767 | |||||||
| chr19:18902768 | G | GAAAGAAA others(95): Show |
2 | a0002c0003t0001g0060 a0002c0003t0001g0159 |
2 | HG02965.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(99): Show |
3 | a0002c0003t0001g0077 a0002c0003t0001g0121 a0002c0003t0001g0145 |
3 | HG02040.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(70): Show |
1 | a0002c0003t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(77): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(74): Show |
1 | a0002c0003t0001g0123 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(78): Show |
1 | a0002c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(82): Show |
1 | a0002c0003t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(86): Show |
20 | a0002c0003t0001g0016 a0002c0003t0001g0041 a0002c0003t0001g0042 others(17): Show |
21 | HG00609.hp1 HG01346.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(90): Show |
3 | a0002c0003t0001g0189 a0002c0003t0001g0204 a0002c0007t0001g0140 |
3 | HG02622.hp1 HG03471.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(94): Show |
1 | a0002c0003t0001g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(102): Show |
1 | a0002c0003t0001g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(65): Show |
1 | a0002c0003t0001g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(72): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(77): Show |
4 | a0002c0003t0001g0080 a0002c0003t0001g0131 a0002c0003t0001g0196 others(1): Show |
4 | HG02486.hp2 HG03453.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(84): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(81): Show |
3 | a0002c0003t0001g0146 a0002c0003t0001g0149 a0002c0003t0001g0151 |
3 | HG02809.hp1 NA19060.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(85): Show |
1 | a0002c0003t0001g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(89): Show |
4 | a0002c0003t0001g0124 a0002c0003t0001g0132 a0002c0003t0001g0139 others(1): Show |
4 | HG02818.hp1 NA18941.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+499_735+500ins others(96): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(93): Show |
2 | a0002c0003t0001g0133 a0002c0003t0001g0201 |
2 | HG03130.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(100): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(97): Show |
2 | a0002c0003t0001g0192 a0002c0003t0001g0252 |
2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(104): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(101): Show |
2 | a0002c0003t0001g0113 a0002c0003t0001g0137 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.735+499_735+500ins others(108): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(105): Show |
1 | a0002c0003t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(112): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(113): Show |
1 | a0002c0003t0001g0253 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(120): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(81): Show |
1 | a0001c0001t0001g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGAAA others(94): Show |
1 | a0002c0003t0001g0150 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(91): Show |
1 | a0002c0003t0001g0005 | 3 | HG00738.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(74): Show |
2 | a0002c0003t0001g0125 a0002c0003t0001g0143 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(94): Show |
1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(106): Show |
1 | a0002c0003t0001g0040 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(113): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(74): Show |
1 | a0002c0003t0001g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(78): Show |
1 | a0002c0003t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(86): Show |
2 | a0002c0003t0001g0144 a0002c0003t0001g0147 |
2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(77): Show |
1 | a0002c0003t0001g0130 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(84): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(81): Show |
1 | a0002c0003t0001g0078 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(88): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(60): Show |
1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(67): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(64): Show |
1 | a0002c0003t0001g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(71): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(76): Show |
1 | a0002c0003t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(83): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAAGGAA others(71): Show |
1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(78): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAGGAAA others(99): Show |
1 | a0002c0003t0001g0248 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAGGAAA others(85): Show |
1 | a0002c0003t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GAAGGAAG others(85): Show |
1 | a0002c0003t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(92): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GGAAAGAA others(74): Show |
1 | a0002c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.735+499_735+500ins others(81): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GGAAAGAA others(78): Show |
1 | a0004c0006t0001g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.735+499_735+500ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902768 | G | GGAAAGAA others(82): Show |
2 | a0002c0003t0001g0136 a0002c0003t0001g0198 |
2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+499_735+500ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902768 | |||||||
| chr19:18902769 | G | A | 42 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 others(39): Show |
43 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.735+499C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902769 | |||||||
| chr19:18902771 | A | G | 6 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0004t0001g0288 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+497T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902771 | |||||||
| chr19:18902772 | A | AGAAG | 9 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0068 others(6): Show |
10 | HG01433.hp1 HG02074.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.735+492_735+495dup others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | A | G | 116 | a0001c0001t0001g0067 a0001c0001t0001g0156 a0001c0001t0001g0160 others(113): Show |
119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.735+496T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | AGAAG | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(35): Show |
57 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.735+492_735+495del others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | AGAAGGAA others(1): Show |
A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0034 others(4): Show |
8 | HG01070.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+488_735+495del others(8): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | AGAAGGAA others(5): Show |
A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0088 |
3 | HG02523.hp1 HG02602.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.735+484_735+495del others(12): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | AGAAGGAA others(9): Show |
A | 7 | a0001c0001t0001g0074 a0003c0005t0001g0268 a0003c0005t0001g0269 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+480_735+495del others(16): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902772 | AGAAGGAA others(13): Show |
A | 1 | a0003c0005t0001g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.735+476_735+495del others(20): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902772 | |||||||
| chr19:18902773 | G | A | 6 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0004t0001g0288 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+495C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902773 | |||||||
| chr19:18902773 | G | GA | 8 | a0001c0002t0001g0044 a0001c0002t0001g0100 a0001c0002t0001g0101 others(5): Show |
8 | HG00099.hp2 HG00323.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+494dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902773 | |||||||
| chr19:18902775 | A | AAGGAAGG others(26): Show |
3 | a0001c0002t0001g0014 a0001c0002t0001g0163 a0001c0002t0001g0214 |
4 | HG02132.hp1 HG02155.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+492_735+493ins others(33): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902775 | |||||||
| chr19:18902775 | A | AAGGAAGG others(35): Show |
1 | a0001c0002t0001g0099 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.735+492_735+493ins others(42): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902775 | |||||||
| chr19:18902776 | G | A | 33 | a0001c0001t0001g0066 a0002c0003t0001g0005 a0002c0003t0001g0016 others(30): Show |
36 | HG00609.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.735+492C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902776 | |||||||
| chr19:18902777 | G | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0099 a0001c0002t0001g0106 others(2): Show |
6 | HG01167.hp1 HG02132.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+491C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902777 | |||||||
| chr19:18902778 | AAGGAAGG | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0002t0001g0098 others(1): Show |
4 | HG02615.hp2 HG03239.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+483_735+489del others(7): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902778 | |||||||
| chr19:18902778 | AAGGAAGG others(8): Show |
A | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.735+475_735+489del others(15): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902778 | |||||||
| chr19:18902780 | G | A | 20 | a0002c0003t0001g0016 a0002c0003t0001g0078 a0002c0003t0001g0079 others(17): Show |
21 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.735+488C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902780 | |||||||
| chr19:18902781 | G | GA | 6 | a0001c0002t0001g0100 a0001c0002t0001g0101 a0001c0002t0001g0162 others(3): Show |
6 | HG00323.hp2 HG01192.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+486dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902781 | |||||||
| chr19:18902784 | G | A | 6 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0125 others(3): Show |
6 | HG01891.hp2 HG02602.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+484C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902784 | |||||||
| chr19:18902785 | G | A | 1 | a0001c0002t0001g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.735+483C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902785 | |||||||
| chr19:18902792 | G | A | 1 | a0001c0010t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.735+476C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902792 | |||||||
| chr19:18902801 | G | GAAAGAAA others(75): Show |
2 | a0003c0008t0001g0277 a0003c0008t0001g0279 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.735+466_735+467ins others(82): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902801 | |||||||
| chr19:18902805 | G | A | 2 | a0003c0008t0001g0277 a0003c0008t0001g0279 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.735+463C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | |||||||
| chr19:18902805 | G | GAAAGAAA others(83): Show |
1 | a0003c0016t0001g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+462_735+463ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | |||||||
| chr19:18902805 | G | GAAAGAAA others(67): Show |
1 | a0003c0008t0001g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.735+462_735+463ins others(74): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902805 | |||||||
| chr19:18902809 | G | A | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+459C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902809 | |||||||
| chr19:18902809 | G | GA | 20 | a0001c0002t0001g0032 a0001c0002t0001g0109 a0001c0002t0001g0111 others(17): Show |
20 | HG01346.hp1 HG01433.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+458dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902809 | |||||||
| chr19:18902812 | G | A | 2 | a0002c0003t0001g0136 a0002c0003t0001g0198 |
2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+456C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902812 | |||||||
| chr19:18902813 | G | A | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+455C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | |||||||
| chr19:18902813 | G | GA | 11 | a0001c0002t0001g0169 a0001c0002t0001g0171 a0001c0002t0001g0173 others(8): Show |
11 | HG01071.hp2 HG01261.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+454dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | |||||||
| chr19:18902813 | G | GAAGAAAG others(40): Show |
2 | a0003c0004t0001g0018 a0003c0004t0001g0281 |
3 | HG02723.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.735+454_735+455ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902813 | |||||||
| chr19:18902816 | G | A | 2 | a0002c0003t0001g0136 a0002c0003t0001g0198 |
2 | HG00099.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.735+452C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902816 | |||||||
| chr19:18902817 | G | A | 6 | a0003c0004t0001g0018 a0003c0004t0001g0281 a0003c0008t0001g0277 others(3): Show |
7 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+451C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902817 | G | GA | 4 | a0001c0002t0001g0233 a0001c0002t0001g0239 a0001c0002t0001g0243 others(1): Show |
4 | HG01255.hp1 HG03239.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+450dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902817 | G | GAAAGAAA others(38): Show |
1 | a0003c0004t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(45): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902817 | G | GAAAGCAA others(105): Show |
3 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0019t0001g0286 |
3 | HG02258.hp1 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.735+450_735+451ins others(112): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902817 | G | GAAAGCAA others(109): Show |
1 | a0003c0004t0001g0288 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(116): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902817 | G | GAAGAAAG others(44): Show |
1 | a0003c0004t0001g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.735+450_735+451ins others(51): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902817 | |||||||
| chr19:18902820 | G | A | 48 | a0001c0001t0001g0112 a0002c0003t0001g0005 a0002c0003t0001g0016 others(45): Show |
51 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.735+448C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902820 | |||||||
| chr19:18902821 | G | A | 12 | a0003c0004t0001g0018 a0003c0004t0001g0263 a0003c0004t0001g0264 others(9): Show |
13 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.735+447C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGAAA others(18): Show |
1 | a0003c0004t0001g0291 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(25): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(100): Show |
1 | a0001c0002t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(108): Show |
1 | a0001c0002t0001g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(112): Show |
1 | a0001c0002t0001g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(104): Show |
1 | a0001c0002t0001g0223 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(108): Show |
2 | a0001c0002t0001g0205 a0001c0002t0001g0236 |
2 | HG00609.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(112): Show |
1 | a0001c0002t0001g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(140): Show |
1 | a0001c0002t0001g0255 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.735+446_735+447ins others(147): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(104): Show |
2 | a0001c0002t0001g0208 a0001c0002t0001g0217 |
2 | HG00408.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.735+446_735+447ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(108): Show |
1 | a0001c0002t0001g0232 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(132): Show |
1 | a0001c0002t0001g0245 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(139): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(148): Show |
1 | a0001c0002t0001g0247 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(155): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(112): Show |
1 | a0001c0002t0001g0258 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(119): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(128): Show |
1 | a0001c0002t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(135): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(99): Show |
1 | a0001c0002t0001g0168 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902821 | G | GAAAGGAA others(111): Show |
1 | a0001c0002t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.735+446_735+447ins others(118): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902821 | |||||||
| chr19:18902824 | G | A | 61 | a0001c0001t0001g0112 a0002c0003t0001g0005 a0002c0003t0001g0016 others(58): Show |
64 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.735+444C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902824 | |||||||
| chr19:18902825 | G | A | 30 | a0001c0002t0001g0168 a0001c0002t0001g0205 a0001c0002t0001g0206 others(27): Show |
31 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.735+443C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAAAGA others(33): Show |
9 | a0002c0003t0001g0125 a0002c0003t0001g0126 a0002c0003t0001g0143 others(6): Show |
9 | HG01891.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(40): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAAAGA others(38): Show |
31 | a0002c0003t0001g0016 a0002c0003t0001g0041 a0002c0003t0001g0042 others(28): Show |
32 | HG00609.hp1 HG01346.hp2 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(45): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAAAGA others(43): Show |
2 | a0002c0003t0001g0005 a0002c0003t0001g0259 |
4 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(50): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(32): Show |
2 | a0002c0003t0001g0129 a0002c0003t0001g0130 |
2 | HG01081.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(37): Show |
5 | a0002c0003t0001g0194 a0002c0003t0001g0196 a0002c0003t0001g0197 others(2): Show |
5 | HG02896.hp1 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(44): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(42): Show |
1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(49): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(47): Show |
3 | a0002c0003t0001g0192 a0002c0003t0001g0201 a0002c0003t0001g0202 |
3 | HG01109.hp2 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(54): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(56): Show |
1 | a0002c0003t0001g0113 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(63): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(24): Show |
4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0002c0003t0001g0136 others(1): Show |
4 | HG00099.hp1 HG02895.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(31): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(41): Show |
1 | a0002c0003t0001g0203 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(48): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(46): Show |
2 | a0002c0003t0001g0040 a0002c0003t0001g0077 |
2 | HG02040.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(53): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(51): Show |
5 | a0002c0003t0001g0043 a0002c0003t0001g0251 a0002c0003t0001g0252 others(2): Show |
5 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(58): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(32): Show |
3 | a0002c0003t0001g0121 a0002c0003t0001g0146 a0002c0003t0001g0204 |
3 | HG02257.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(31): Show |
1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(38): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(36): Show |
1 | a0002c0003t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(43): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(35): Show |
2 | a0004c0006t0001g0122 a0004c0006t0001g0142 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(42): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGAAA others(78): Show |
1 | a0003c0004t0001g0280 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(100): Show |
1 | a0001c0002t0001g0220 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(104): Show |
1 | a0001c0002t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(111): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(108): Show |
2 | a0001c0002t0001g0222 a0001c0002t0001g0240 |
2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(116): Show |
1 | a0001c0002t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(123): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(91): Show |
1 | a0001c0002t0001g0215 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAAGGAA others(83): Show |
1 | a0001c0002t0001g0241 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGAAAG others(59): Show |
1 | a0002c0003t0001g0137 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(66): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(28): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG01123.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(35): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(50): Show |
1 | a0002c0003t0001g0193 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(57): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(40): Show |
1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(108): Show |
1 | a0001c0002t0001g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(115): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(128): Show |
1 | a0001c0002t0001g0244 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(135): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(166): Show |
1 | a0001c0002t0001g0176 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(173): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(95): Show |
1 | a0001c0002t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(91): Show |
1 | a0001c0002t0001g0209 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(155): Show |
1 | a0001c0002t0001g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(162): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(107): Show |
1 | a0001c0002t0001g0227 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(114): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(99): Show |
1 | a0001c0002t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(106): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAA others(155): Show |
1 | a0001c0002t0001g0032 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(162): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(32): Show |
1 | a0004c0006t0001g0114 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(39): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(49): Show |
1 | a0002c0003t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(56): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(54): Show |
1 | a0002c0003t0001g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(61): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(58): Show |
1 | a0003c0004t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(65): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(87): Show |
1 | a0003c0004t0001g0284 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(94): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(91): Show |
1 | a0001c0002t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(98): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(131): Show |
1 | a0001c0002t0001g0225 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(138): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(95): Show |
1 | a0001c0002t0001g0219 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(137): Show |
1 | a0001c0002t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(144): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(58): Show |
2 | a0002c0003t0001g0144 a0002c0003t0001g0147 |
2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(65): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(71): Show |
1 | a0003c0004t0001g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(78): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(83): Show |
1 | a0003c0004t0001g0290 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(90): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(111): Show |
1 | a0001c0002t0001g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(118): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(119): Show |
1 | a0001c0002t0001g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(126): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(115): Show |
1 | a0001c0002t0001g0243 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(122): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(79): Show |
1 | a0003c0004t0001g0019 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(86): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0003c0018t0001g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(40): Show |
1 | a0001c0001t0001g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(47): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0001c0002t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(95): Show |
1 | a0003c0017t0001g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(102): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(79): Show |
1 | a0001c0002t0001g0175 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(86): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(78): Show |
1 | a0001c0002t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(85): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(127): Show |
1 | a0001c0002t0001g0246 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(134): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(88): Show |
1 | a0001c0002t0001g0181 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(95): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(82): Show |
3 | a0001c0002t0001g0166 a0001c0002t0001g0169 a0001c0002t0001g0182 |
3 | HG01261.hp1 HG01993.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(89): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(90): Show |
1 | a0001c0002t0001g0216 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(98): Show |
1 | a0001c0002t0001g0185 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(105): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(86): Show |
2 | a0001c0002t0001g0165 a0001c0002t0001g0183 |
2 | HG01981.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(93): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(90): Show |
5 | a0001c0002t0001g0111 a0001c0002t0001g0170 a0001c0002t0001g0177 others(2): Show |
5 | HG01361.hp2 NA18954.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(94): Show |
1 | a0001c0002t0001g0109 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(102): Show |
1 | a0001c0002t0001g0172 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(90): Show |
2 | a0001c0002t0001g0187 a0001c0002t0001g0235 |
2 | NA18980.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(97): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(94): Show |
2 | a0001c0002t0001g0228 a0001c0002t0001g0231 |
2 | HG01109.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(102): Show |
2 | a0001c0002t0001g0171 a0001c0002t0001g0178 |
2 | NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(114): Show |
1 | a0001c0002t0001g0173 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(121): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(93): Show |
1 | a0001c0002t0001g0180 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(100): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(102): Show |
2 | a0001c0002t0001g0179 a0001c0002t0001g0237 |
2 | NA18995.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.735+442_735+443ins others(109): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(97): Show |
1 | a0001c0002t0001g0233 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.735+442_735+443ins others(104): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(94): Show |
1 | a0001c0002t0001g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(101): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGAAG others(106): Show |
1 | a0001c0002t0001g0218 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(113): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902825 | G | GAAGGGAA others(189): Show |
1 | a0001c0002t0001g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.735+442_735+443ins others(196): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902825 | |||||||
| chr19:18902826 | A | AAAGAAAG others(46): Show |
1 | a0003c0011t0001g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.735+441_735+442ins others(53): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | |||||||
| chr19:18902826 | A | AAAGAAAG others(50): Show |
1 | a0003c0011t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.735+441_735+442ins others(57): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | |||||||
| chr19:18902826 | A | AAGGAAAG others(54): Show |
1 | a0001c0010t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.735+441_735+442ins others(61): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902826 | |||||||
| chr19:18902828 | G | GGAAGGAA others(100): Show |
1 | a0001c0002t0001g0186 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.735+439_735+440ins others(107): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902828 | |||||||
| chr19:18902830 | A | C | 7 | a0003c0004t0001g0019 a0003c0004t0001g0280 a0003c0004t0001g0284 others(4): Show |
8 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.735+438T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902830 | |||||||
| chr19:18902836 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.735+432A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902836 | |||||||
| chr19:18902996 | G | A | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.735+272C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 7/9 | chr19 | 18902996 | |||||||
| chr19:18903439 | C | T | 87 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(84): Show |
90 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.580-16G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903439 | |||||||
| chr19:18903452 | G | A | 1 | a0001c0002t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.580-29C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903452 | |||||||
| chr19:18903498 | G | A | 1 | a0003c0011t0001g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.580-75C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903498 | |||||||
| chr19:18903565 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0096 |
3 | HG02630.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.580-142T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903565 | |||||||
| chr19:18903578 | G | GT | 3 | a0001c0010t0001g0141 a0003c0011t0001g0267 a0003c0011t0001g0275 |
3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.580-156dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903578 | |||||||
| chr19:18903613 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.580-190C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903613 | |||||||
| chr19:18903841 | C | T | 2 | a0001c0002t0001g0098 a0001c0002t0001g0102 |
2 | HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.580-418G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903841 | |||||||
| chr19:18903874 | G | A | 1 | a0002c0003t0001g0151 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.580-451C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903874 | |||||||
| chr19:18903881 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.580-458G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903881 | |||||||
| chr19:18903952 | G | A | 73 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(70): Show |
73 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.580-529C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18903952 | |||||||
| chr19:18904000 | T | C | 74 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.580-577A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904000 | |||||||
| chr19:18904224 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.579+547G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904224 | |||||||
| chr19:18904297 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.579+474T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904297 | |||||||
| chr19:18904312 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.579+459C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904312 | |||||||
| chr19:18904334 | G | A | 3 | a0001c0002t0001g0089 a0001c0002t0001g0103 a0003c0004t0001g0266 |
3 | HG02109.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.579+437C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904334 | |||||||
| chr19:18904682 | C | T | 19 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(16): Show |
20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.579+89G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904682 | |||||||
| chr19:18904736 | C | T | 2 | a0002c0003t0001g0194 a0002c0003t0001g0195 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.579+35G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 6/9 | chr19 | 18904736 | |||||||
| chr19:18905008 | A | ACCTGCCC others(12): Show |
1 | a0002c0003t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.498-157_498-156ins others(19): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905008 | |||||||
| chr19:18905026 | C | G | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.498-174G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905026 | |||||||
| chr19:18905026 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.498-174G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905026 | |||||||
| chr19:18905093 | A | G | 21 | a0003c0004t0001g0018 a0003c0004t0001g0019 a0003c0004t0001g0263 others(18): Show |
23 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.498-241T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905093 | |||||||
| chr19:18905161 | A | G | 1 | a0003c0005t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.498-309T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905161 | |||||||
| chr19:18905299 | A | G | 189 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(186): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.497+277T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905299 | |||||||
| chr19:18905475 | A | G | 3 | a0004c0006t0001g0038 a0004c0006t0001g0122 a0004c0006t0001g0142 |
3 | HG02280.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497+101T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905475 | |||||||
| chr19:18905494 | A | AGACGCTC others(8): Show |
1 | a0001c0002t0001g0227 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.497+67_497+81dupAC others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905494 | |||||||
| chr19:18905494 | AGACGCTC others(8): Show |
A | 6 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0004t0001g0288 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.497+67_497+81delAC others(13): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 5/9 | chr19 | 18905494 | |||||||
| chr19:18905641 | G | A | 5 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(2): Show |
5 | HG00642.hp2 HG00741.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.444-12C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905641 | |||||||
| chr19:18905645 | A | AG | 20 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0002t0001g0031 others(17): Show |
20 | HG00609.hp2 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.444-17dupC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905645 | |||||||
| chr19:18905867 | C | T | 1 | a0003c0018t0001g0282 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.444-238G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905867 | |||||||
| chr19:18905892 | T | C | 7 | a0001c0010t0001g0141 a0003c0008t0001g0277 a0003c0008t0001g0278 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-263A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905892 | |||||||
| chr19:18905939 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.444-310C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905939 | |||||||
| chr19:18905976 | G | A | 74 | a0002c0003t0001g0005 a0002c0003t0001g0016 a0002c0003t0001g0039 others(71): Show |
77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.444-347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18905976 | |||||||
| chr19:18906169 | G | A | 18 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(15): Show |
19 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-540C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906169 | |||||||
| chr19:18906196 | T | A | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.444-567A>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906196 | |||||||
| chr19:18906258 | C | T | 2 | a0001c0002t0001g0240 a0001c0002t0001g0255 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.444-629G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906258 | |||||||
| chr19:18906528 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.443+432G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906528 | |||||||
| chr19:18906546 | G | A | 1 | a0001c0002t0001g0210 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+414C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906546 | |||||||
| chr19:18906732 | G | A | 3 | a0001c0002t0001g0245 a0001c0002t0001g0246 a0001c0002t0001g0247 |
3 | HG00738.hp2 HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.443+228C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906732 | |||||||
| chr19:18906763 | T | C | 211 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.443+197A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906763 | |||||||
| chr19:18906852 | C | T | 3 | a0001c0010t0001g0141 a0003c0011t0001g0267 a0003c0011t0001g0275 |
3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.443+108G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906852 | |||||||
| chr19:18906902 | G | A | 7 | a0003c0005t0001g0268 a0003c0005t0001g0269 a0003c0005t0001g0270 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.443+58C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 4/9 | chr19 | 18906902 | |||||||
| chr19:18907191 | G | C | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.291-79C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907191 | |||||||
| chr19:18907442 | C | T | 7 | a0003c0005t0001g0268 a0003c0005t0001g0269 a0003c0005t0001g0270 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-330G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907442 | |||||||
| chr19:18907487 | T | A | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-375A>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907487 | |||||||
| chr19:18907502 | A | C | 19 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(16): Show |
20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.291-390T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907502 | |||||||
| chr19:18907549 | G | A | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.291-437C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907549 | |||||||
| chr19:18907667 | G | A | 7 | a0003c0005t0001g0268 a0003c0005t0001g0269 a0003c0005t0001g0270 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-555C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907667 | |||||||
| chr19:18907675 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.291-563T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907675 | |||||||
| chr19:18907762 | G | A | 7 | a0003c0005t0001g0268 a0003c0005t0001g0269 a0003c0005t0001g0270 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-650C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907762 | |||||||
| chr19:18907788 | G | T | 1 | a0001c0002t0001g0215 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.291-676C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907788 | |||||||
| chr19:18907805 | C | T | 74 | a0002c0003t0001g0005 a0002c0003t0001g0016 a0002c0003t0001g0039 others(71): Show |
77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.291-693G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907805 | |||||||
| chr19:18907925 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.291-813G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18907925 | |||||||
| chr19:18908015 | G | A | 3 | a0001c0010t0001g0141 a0003c0011t0001g0267 a0003c0011t0001g0275 |
3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291-903C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908015 | |||||||
| chr19:18908025 | G | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.291-913C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908025 | |||||||
| chr19:18908034 | A | C | 3 | a0002c0003t0001g0152 a0002c0003t0001g0188 a0002c0003t0001g0189 |
3 | HG02809.hp2 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291-922T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908034 | |||||||
| chr19:18908057 | A | G | 75 | a0001c0001t0001g0049 a0001c0002t0001g0031 a0001c0002t0001g0032 others(72): Show |
75 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.291-945T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908057 | |||||||
| chr19:18908112 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.291-1000C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908112 | |||||||
| chr19:18908153 | C | T | 12 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0099 others(9): Show |
13 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-1041G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908153 | |||||||
| chr19:18908208 | C | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.291-1096G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908208 | |||||||
| chr19:18908521 | C | CTCTT | 205 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(202): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.291-1410_291-1409i others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908521 | |||||||
| chr19:18908579 | C | T | 3 | a0001c0010t0001g0141 a0003c0011t0001g0267 a0003c0011t0001g0275 |
3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291-1467G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908579 | |||||||
| chr19:18908602 | C | T | 3 | a0002c0003t0001g0120 a0002c0003t0001g0123 a0002c0003t0001g0138 |
3 | HG02602.hp2 HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.291-1490G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908602 | |||||||
| chr19:18908666 | G | A | 3 | a0003c0004t0001g0018 a0003c0004t0001g0263 a0003c0004t0001g0281 |
4 | HG02723.hp2 HG02886.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-1554C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908666 | |||||||
| chr19:18908932 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291-1820T>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908932 | |||||||
| chr19:18908991 | G | A | 9 | a0002c0003t0001g0005 a0002c0003t0001g0039 a0002c0003t0001g0040 others(6): Show |
11 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.291-1879C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18908991 | |||||||
| chr19:18909051 | G | A | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG01123.hp2 HG02895.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1920C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909051 | |||||||
| chr19:18909060 | T | G | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1911A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909060 | |||||||
| chr19:18909075 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.290+1896C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909075 | |||||||
| chr19:18909143 | T | G | 10 | a0003c0004t0001g0019 a0003c0004t0001g0264 a0003c0004t0001g0265 others(7): Show |
11 | HG01891.hp1 HG02630.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+1828A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909143 | |||||||
| chr19:18909360 | G | A | 1 | a0002c0003t0001g0248 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.290+1611C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909360 | |||||||
| chr19:18909485 | T | C | 1 | a0001c0002t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.290+1486A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909485 | |||||||
| chr19:18909519 | CT | C | 187 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0087 others(184): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.290+1451delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909519 | |||||||
| chr19:18909519 | CTT | C | 12 | a0001c0002t0001g0178 a0002c0003t0001g0094 a0002c0003t0001g0113 others(9): Show |
13 | HG01167.hp2 HG02630.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.290+1450_290+1451d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909519 | |||||||
| chr19:18909647 | T | C | 74 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.290+1324A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909647 | |||||||
| chr19:18909746 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.290+1225G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909746 | |||||||
| chr19:18909906 | G | A | 4 | a0003c0004t0001g0285 a0003c0004t0001g0287 a0003c0004t0001g0288 others(1): Show |
4 | HG02258.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.290+1065C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909906 | |||||||
| chr19:18909934 | T | C | 2 | a0003c0008t0001g0277 a0003c0008t0001g0279 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.290+1037A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909934 | |||||||
| chr19:18909935 | A | G | 9 | a0002c0003t0001g0113 a0002c0003t0001g0137 a0002c0003t0001g0192 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1036T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18909935 | |||||||
| chr19:18910193 | T | C | 74 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.290+778A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910193 | |||||||
| chr19:18910201 | C | T | 79 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(76): Show |
82 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.290+770G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910201 | |||||||
| chr19:18910263 | C | A | 1 | a0002c0003t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.290+708G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910263 | |||||||
| chr19:18910268 | C | G | 1 | a0002c0003t0001g0248 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.290+703G>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910268 | |||||||
| chr19:18910303 | G | A | 7 | a0003c0004t0001g0019 a0003c0004t0001g0280 a0003c0004t0001g0284 others(4): Show |
8 | HG02630.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.290+668C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910303 | |||||||
| chr19:18910366 | G | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18944.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.290+605C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910366 | |||||||
| chr19:18910415 | G | A | 3 | a0001c0010t0001g0141 a0003c0011t0001g0267 a0003c0011t0001g0275 |
3 | HG02559.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.290+556C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910415 | |||||||
| chr19:18910585 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.290+386A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910585 | |||||||
| chr19:18910631 | C | T | 5 | a0001c0010t0001g0141 a0003c0005t0001g0268 a0003c0005t0001g0272 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+340G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910631 | |||||||
| chr19:18910645 | T | C | 67 | a0002c0003t0001g0016 a0002c0003t0001g0060 a0002c0003t0001g0077 others(64): Show |
68 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.290+326A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910645 | |||||||
| chr19:18910676 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0095 |
2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.290+295C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910676 | |||||||
| chr19:18910855 | C | A | 1 | a0001c0002t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.290+116G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910855 | |||||||
| chr19:18910877 | G | A | 1 | a0003c0004t0001g0287 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.290+94C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910877 | |||||||
| chr19:18910904 | G | A | 1 | a0003c0008t0001g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.290+67C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 3/9 | chr19 | 18910904 | |||||||
| chr19:18911161 | T | C | 204 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(201): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.190-90A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911161 | |||||||
| chr19:18911198 | C | A | 74 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0082 others(71): Show |
74 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.190-127G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911198 | |||||||
| chr19:18911236 | G | A | 25 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(22): Show |
27 | HG00099.hp2 HG00323.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.190-165C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911236 | |||||||
| chr19:18911382 | A | G | 1 | a0003c0004t0001g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.190-311T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911382 | |||||||
| chr19:18911395 | T | C | 36 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(33): Show |
39 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.190-324A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911395 | |||||||
| chr19:18911447 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.190-376G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911447 | |||||||
| chr19:18911555 | ATTTT | A | 74 | a0002c0003t0001g0005 a0002c0003t0001g0016 a0002c0003t0001g0039 others(71): Show |
77 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.190-488_190-485del others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911555 | |||||||
| chr19:18911709 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0160 a0001c0001t0001g0262 |
3 | HG00323.hp1 HG02615.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.190-638C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911709 | |||||||
| chr19:18911851 | C | CT | 17 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0086 others(14): Show |
17 | HG01928.hp1 HG01928.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.190-781dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911851 | |||||||
| chr19:18911851 | CT | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
6 | HG01123.hp2 HG02895.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-781delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18911851 | |||||||
| chr19:18912135 | C | A | 1 | a0002c0003t0001g0138 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.189+849G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912135 | |||||||
| chr19:18912309 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189+675A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912309 | |||||||
| chr19:18912461 | G | GA | 41 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(38): Show |
44 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.189+522dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912461 | |||||||
| chr19:18912629 | C | T | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+355G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912629 | |||||||
| chr19:18912717 | C | T | 87 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(84): Show |
90 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.189+267G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912717 | |||||||
| chr19:18912738 | C | CA | 11 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0047 others(8): Show |
11 | HG02055.hp2 HG02293.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.189+245dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912738 | |||||||
| chr19:18912738 | CA | C | 183 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0112 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.189+245delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912738 | |||||||
| chr19:18912764 | A | G | 19 | a0001c0002t0001g0014 a0001c0002t0001g0044 a0001c0002t0001g0089 others(16): Show |
20 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+220T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 2/9 | chr19 | 18912764 | |||||||
| chr19:18913072 | C | T | 4 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(1): Show |
4 | HG00642.hp2 HG00741.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-26G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913072 | |||||||
| chr19:18913228 | C | T | 2 | a0002c0003t0001g0039 a0002c0003t0001g0040 |
2 | HG02735.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.127-182G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913228 | |||||||
| chr19:18913232 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-186C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913232 | |||||||
| chr19:18913254 | C | T | 2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | NA18998.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.127-208G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913254 | |||||||
| chr19:18913305 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-259C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913305 | |||||||
| chr19:18913357 | G | A | 1 | a0002c0003t0001g0153 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.127-311C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913357 | |||||||
| chr19:18913534 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.127-488C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913534 | |||||||
| chr19:18913581 | C | A | 1 | a0001c0002t0001g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.127-535G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913581 | |||||||
| chr19:18913611 | A | G | 227 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.127-565T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913611 | |||||||
| chr19:18913613 | C | T | 1 | a0002c0003t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.127-567G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913613 | |||||||
| chr19:18913616 | T | TC | 227 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(224): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.127-571dupG | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913616 | |||||||
| chr19:18913872 | A | T | 1 | a0001c0002t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.127-826T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18913872 | |||||||
| chr19:18914163 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0156 a0001c0001t0001g0160 others(1): Show |
4 | HG00323.hp1 HG02615.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1117G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914163 | |||||||
| chr19:18914306 | G | A | 7 | a0003c0005t0001g0268 a0003c0005t0001g0269 a0003c0005t0001g0270 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-1260C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914306 | |||||||
| chr19:18914409 | C | T | 1 | a0002c0003t0001g0060 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.127-1363G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914409 | |||||||
| chr19:18914472 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(8): Show |
13 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-1426A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914472 | |||||||
| chr19:18914605 | C | A | 1 | a0001c0002t0001g0258 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.127-1559G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914605 | |||||||
| chr19:18914755 | C | CT | 35 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0047 others(32): Show |
39 | HG00597.hp1 HG00597.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.127-1710dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914755 | |||||||
| chr19:18914755 | CT | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0083 a0001c0001t0001g0084 others(7): Show |
10 | HG01168.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-1710delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914755 | |||||||
| chr19:18914775 | T | G | 1 | a0002c0007t0001g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.127-1729A>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914775 | |||||||
| chr19:18914840 | T | C | 1 | a0002c0003t0001g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.127-1794A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914840 | |||||||
| chr19:18914903 | T | C | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1857A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914903 | |||||||
| chr19:18914941 | T | C | 3 | a0001c0010t0001g0141 a0002c0003t0001g0121 a0003c0011t0001g0275 |
3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.127-1895A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18914941 | |||||||
| chr19:18915015 | C | T | 1 | a0001c0002t0001g0230 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.127-1969G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915015 | |||||||
| chr19:18915167 | C | T | 3 | a0004c0006t0001g0038 a0004c0006t0001g0122 a0004c0006t0001g0142 |
3 | HG02280.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.127-2121G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915167 | |||||||
| chr19:18915278 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.127-2232C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915278 | |||||||
| chr19:18915350 | G | C | 1 | a0001c0002t0001g0104 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.127-2304C>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915350 | |||||||
| chr19:18915683 | T | C | 5 | a0002c0003t0001g0016 a0002c0003t0001g0154 a0002c0003t0001g0158 others(2): Show |
6 | HG02258.hp2 HG02451.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-2637A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915683 | |||||||
| chr19:18915981 | C | T | 2 | a0001c0002t0001g0205 a0001c0002t0001g0206 |
2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.127-2935G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18915981 | |||||||
| chr19:18916042 | A | G | 27 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(24): Show |
28 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.127-2996T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916042 | |||||||
| chr19:18916093 | G | A | 1 | a0003c0004t0001g0264 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-3047C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916093 | |||||||
| chr19:18916190 | C | CA | 4 | a0003c0008t0001g0277 a0003c0008t0001g0278 a0003c0008t0001g0279 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+3032dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916190 | |||||||
| chr19:18916352 | C | CA | 11 | a0001c0001t0001g0160 a0003c0004t0001g0265 a0003c0004t0001g0289 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+2870dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916352 | |||||||
| chr19:18916403 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.126+2820G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916403 | |||||||
| chr19:18916422 | G | A | 1 | a0001c0002t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.126+2801C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916422 | |||||||
| chr19:18916876 | G | A | 1 | a0001c0010t0001g0036 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126+2347C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916876 | |||||||
| chr19:18916944 | C | CA | 31 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(28): Show |
38 | HG00558.hp2 HG01169.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.126+2278dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | |||||||
| chr19:18916944 | C | CAA | 22 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0002t0001g0014 others(19): Show |
23 | HG00323.hp2 HG01099.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.126+2277_126+2278d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | |||||||
| chr19:18916944 | C | CAAA | 8 | a0001c0001t0001g0105 a0001c0002t0001g0106 a0002c0003t0001g0203 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2276_126+2278d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | |||||||
| chr19:18916944 | CA | C | 83 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0054 others(80): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.126+2278delT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | |||||||
| chr19:18916944 | CAA | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0047 others(7): Show |
13 | HG01168.hp2 HG01515.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+2277_126+2278d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18916944 | |||||||
| chr19:18917071 | C | A | 1 | a0001c0002t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126+2152G>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917071 | |||||||
| chr19:18917114 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+2109G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917114 | |||||||
| chr19:18917139 | A | G | 1 | a0002c0003t0001g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+2084T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917139 | |||||||
| chr19:18917195 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.126+2028C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917195 | |||||||
| chr19:18917233 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
14 | HG00597.hp2 HG01168.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+1981_126+1989d others(11): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917233 | |||||||
| chr19:18917237 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18944.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.126+1986A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917237 | |||||||
| chr19:18917241 | C | CT | 9 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(6): Show |
9 | HG01123.hp2 HG01167.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+1981dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | |||||||
| chr19:18917241 | C | CTTT | 63 | a0001c0001t0001g0110 a0001c0001t0001g0207 a0001c0002t0001g0031 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.126+1979_126+1981d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | |||||||
| chr19:18917241 | CT | C | 41 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
42 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+1981delA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917241 | |||||||
| chr19:18917245 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.126+1978A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917245 | |||||||
| chr19:18917246 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.126+1977A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917246 | |||||||
| chr19:18917504 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.126+1719C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917504 | |||||||
| chr19:18917832 | C | T | 16 | a0003c0004t0001g0018 a0003c0004t0001g0019 a0003c0004t0001g0263 others(13): Show |
18 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+1391G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917832 | |||||||
| chr19:18917947 | T | C | 1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+1276A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18917947 | |||||||
| chr19:18918187 | C | CA | 68 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0030 others(65): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.126+1035dupT | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | |||||||
| chr19:18918187 | C | CAA | 45 | a0001c0002t0001g0031 a0001c0002t0001g0165 a0001c0002t0001g0166 others(42): Show |
45 | HG01109.hp2 HG01261.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.126+1034_126+1035d others(4): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | |||||||
| chr19:18918187 | C | CAAA | 53 | a0001c0001t0001g0207 a0001c0002t0001g0032 a0001c0002t0001g0205 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.126+1033_126+1035d others(5): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | |||||||
| chr19:18918187 | C | CAAAA | 6 | a0001c0002t0001g0255 a0001c0002t0001g0256 a0001c0002t0001g0257 others(3): Show |
6 | HG01123.hp1 HG01978.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+1032_126+1035d others(6): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918187 | |||||||
| chr19:18918203 | AG | A | 13 | a0003c0004t0001g0019 a0003c0004t0001g0280 a0003c0004t0001g0281 others(10): Show |
14 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+1019delC | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918203 | |||||||
| chr19:18918204 | G | A | 190 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.126+1019C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918204 | |||||||
| chr19:18918348 | TAA | T | 8 | a0001c0002t0001g0044 a0002c0003t0001g0005 a0002c0003t0001g0039 others(5): Show |
10 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+873_126+874del others(2): Show |
COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918348 | |||||||
| chr19:18918542 | A | G | 1 | a0004c0006t0001g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+681T>C | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918542 | |||||||
| chr19:18918557 | C | T | 2 | a0003c0004t0001g0018 a0003c0004t0001g0263 |
3 | HG02723.hp2 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.126+666G>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918557 | |||||||
| chr19:18918631 | G | A | 1 | a0007c0015t0001g0292 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.126+592C>T | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918631 | |||||||
| chr19:18918734 | G | GT | 6 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
8 | HG01070.hp2 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+488dupA | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918734 | |||||||
| chr19:18918983 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.126+240A>G | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18918983 | |||||||
| chr19:18919124 | G | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
16 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+99C>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18919124 | |||||||
| chr19:18919125 | A | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
16 | HG00280.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+98T>A | COPE | ENSG00000105669.14 | transcript | ENST00000262812.9 | protein_coding | 1/9 | chr19 | 18919125 |