Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23603 |
| ensemblid | ENSG00000110880.11 |
| hgncid | 2254 |
| symbol | CORO1C |
| name | coronin 1C |
| refseq_nuc | NM_014325.4 |
| refseq_prot | NP_055140.1 |
| ensembl_nuc | ENST00000261401.8 |
| ensembl_prot | ENSP00000261401.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 108645109 |
| end | 108731518 |
| strand | - |
| ver | v1.2 |
| region | chr12:108645109-108731518 |
| region5000 | chr12:108640109-108736518 |
| regionname0 | CORO1C_chr12_108645109_108731518 |
| regionname5000 | CORO1C_chr12_108640109_108736518 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 474 | 320 | 76 | 54 | 136 | 14 | 38 | 109 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| a0002 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| a0003 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| a0004 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| a0005 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| a0006 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | MRRVV others(469): Show |
chr12 | 108640109 | 108736518 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1422 | 314 | 72 | 53 | 136 | 14 | 37 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0001c0002 | 0/0 | 1422 | 5 | 4 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0001c0006 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0002c0003 | 0/0 | 1422 | 2 | 0 | 0 | 2 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0003c0008 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0004c0004 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0005c0007 | 0/0 | 1422 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 | ||
| a0006c0005 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | ATGAG others(1417): Show |
chr12 | 108640109 | 108736518 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3813 | 173 | 29 | 34 | 84 | 2 | 23 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0002 | 0/0 | 3812 | 61 | 0 | 6 | 49 | 3 | 3 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3807): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0003 | 1/0 | 3814 | 43 | 19 | 10 | 0 | 6 | 7 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0004 | 0/0 | 3814 | 11 | 10 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0005 | 0/0 | 3811 | 5 | 5 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3806): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0006 | 0/0 | 3814 | 4 | 1 | 0 | 2 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0007 | 0/0 | 3813 | 3 | 2 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0008 | 0/0 | 3815 | 2 | 0 | 1 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3810): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0009 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0010 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0011 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0012 | 0/0 | 3812 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3807): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0013 | 0/0 | 3813 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0015 | 0/0 | 3812 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3807): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0016 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0017 | 0/0 | 3814 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0018 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0019 | 0/0 | 3801 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3796): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0020 | 0/0 | 3814 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0001t0021 | 0/0 | 3812 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3807): Show |
chr12 | 108640109 | 108736518 |
| a0001c0002t0003 | 0/0 | 3814 | 5 | 4 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0001c0006t0003 | 0/0 | 3814 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3809): Show |
chr12 | 108640109 | 108736518 |
| a0002c0003t0001 | 0/0 | 3813 | 2 | 0 | 0 | 2 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0003c0008t0001 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0004c0004t0014 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0005c0007t0001 | 0/0 | 3813 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| a0006c0005t0001 | 0/0 | 3813 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | AGTGC others(3808): Show |
chr12 | 108640109 | 108736518 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0011g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0017g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0020g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0001t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0002t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0001c0006t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0002c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0003c0008t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0004c0004t0014g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0005c0007t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| a0006c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0241 | EUR | GBR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0254 | EUR | GBR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0248 | EUR | FIN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0316 | EUR | FIN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00438 | hp2 | a0003 | c0008 | t0001 | g0010 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01255 | hp2 | a0001 | c0001 | t0017 | g0259 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0255 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0285 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | IBS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0253 | EUR | IBS | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0292 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01891 | hp1 | a0001 | c0001 | t0020 | g0300 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0305 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0294 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0302 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0130 | EAS | KHV | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0298 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02886 | hp1 | a0004 | c0004 | t0014 | g0134 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0304 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0267 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0131 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0277 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03098 | hp1 | a0001 | c0001 | t0021 | g0321 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ESN | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0284 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0240 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0162 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0251 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0252 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0288 | AFR | MSL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0320 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03942 | hp1 | a0001 | c0006 | t0003 | g0244 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0055 | SAS | BEB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0295 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18975 | hp2 | a0005 | c0007 | t0001 | g0047 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19063 | hp1 | a0001 | c0001 | t0019 | g0101 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0271 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | YRI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0303 | AFR | ASW | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | ASW | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0319 | EUR | TSI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20752 | hp2 | a0001 | c0001 | t0012 | g0133 | EUR | TSI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0242 | EUR | TSI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0132 | EUR | TSI | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0235 | SAS | GIH | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | GIH | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | CLM | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0287 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | ACB | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | USA | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | USA | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| NA21309 | hp2 | a0006 | c0005 | t0001 | g0067 | AFR | LWK | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0317 | REF | REF | CORO1C_chr12_108640109_108736518 | CORO1C | chr12 | 108640109 | 108736518 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108647471 | C | A | 1 | a0006 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1357G>T | p.Asp453Tyr | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1452/3814 | 1357/1425 | 453/474 | chr12 | 108647471 | |||
| chr12:108648607 | C | T | 1 | a0004 | 1 | HG02886.hp1 | missense_variant&splice_region_variant | MODERATE | c.1303G>A | p.Val435Met | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/11 | 1398/3814 | 1303/1425 | 435/474 | chr12 | 108648607 | |||
| chr12:108662138 | A | C | 1 | a0002 | 2 | HG02040.hp2 HG02083.hp1 |
missense_variant | MODERATE | c.339T>G | p.Asn113Lys | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/11 | 434/3814 | 339/1425 | 113/474 | chr12 | 108662138 | |||
| chr12:108678334 | T | C | 1 | a0005 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.256A>G | p.Ile86Val | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/11 | 351/3814 | 256/1425 | 86/474 | chr12 | 108678334 | |||
| chr12:108701127 | G | C | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.192C>G | p.His64Gln | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/11 | 287/3814 | 192/1425 | 64/474 | chr12 | 108701127 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108647481 | T | C | 1 | a0001c0002 | 5 | HG01433.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
synonymous_variant | LOW | c.1347A>G | p.Lys449Lys | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1442/3814 | 1347/1425 | 449/474 | chr12 | 108647481 | |||
| chr12:108662057 | T | C | 1 | a0001c0006 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.420A>G | p.Pro140Pro | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/11 | 515/3814 | 420/1425 | 140/474 | chr12 | 108662057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108645230 | T | TA | 2 | a0001c0001t0006 a0001c0001t0008 |
6 | HG01256.hp2 HG02523.hp2 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2172dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 2172 | chr12 | 108645230 | ||||||
| chr12:108645230 | TA | T | 6 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0012 others(3): Show |
68 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2172delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 2172 | chr12 | 108645230 | ||||||
| chr12:108645233 | A | T | 1 | a0004c0004t0014 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2170T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 2170 | chr12 | 108645233 | ||||||
| chr12:108645258 | A | G | 2 | a0001c0001t0015 a0001c0001t0021 |
2 | HG02965.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2145T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 2145 | chr12 | 108645258 | ||||||
| chr12:108645398 | G | A | 1 | a0001c0001t0016 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 2005 | chr12 | 108645398 | ||||||
| chr12:108645439 | T | C | 1 | a0001c0001t0017 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1964A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1964 | chr12 | 108645439 | ||||||
| chr12:108645525 | TAA | T | 1 | a0001c0001t0005 | 5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1876_*1877delTT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1876 | chr12 | 108645525 | ||||||
| chr12:108645804 | T | G | 2 | a0001c0001t0015 a0001c0001t0021 |
2 | HG02965.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1599A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1599 | chr12 | 108645804 | ||||||
| chr12:108646018 | A | C | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(16): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*1385T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1385 | chr12 | 108646018 | ||||||
| chr12:108646093 | T | C | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(15): Show |
257 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*1310A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1310 | chr12 | 108646093 | ||||||
| chr12:108646371 | C | T | 1 | a0001c0001t0021 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 1032 | chr12 | 108646371 | ||||||
| chr12:108646459 | C | G | 2 | a0001c0001t0012 a0001c0001t0013 |
2 | NA20752.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*944G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 944 | chr12 | 108646459 | ||||||
| chr12:108646597 | A | G | 1 | a0001c0001t0011 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 806 | chr12 | 108646597 | ||||||
| chr12:108646911 | A | G | 1 | a0001c0001t0010 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*492T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 492 | chr12 | 108646911 | ||||||
| chr12:108646958 | A | G | 1 | a0001c0001t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 445 | chr12 | 108646958 | ||||||
| chr12:108647041 | TA | T | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(14): Show |
256 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*361delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 361 | chr12 | 108647041 | ||||||
| chr12:108647206 | ACGTTTTG others(4): Show |
A | 1 | a0001c0001t0019 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186_*196delGAAACA others(5): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 186 | chr12 | 108647206 | ||||||
| chr12:108647226 | T | C | 1 | a0001c0001t0020 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 11/11 | 177 | chr12 | 108647226 | ||||||
| chr12:108731482 | C | A | 1 | a0001c0001t0021 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/11 | 30164 | chr12 | 108731482 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:108647651 | A | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1306-129T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108647651 | |||||||
| chr12:108647952 | T | TGAGG | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(248): Show |
256 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.1306-434_1306-431d others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108647952 | |||||||
| chr12:108648136 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1305+469G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108648136 | |||||||
| chr12:108648321 | A | T | 3 | a0001c0001t0002g0087 a0001c0001t0002g0106 a0001c0001t0002g0119 |
3 | NA18952.hp1 NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1305+284T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108648321 | |||||||
| chr12:108648526 | C | A | 2 | a0001c0001t0015g0131 a0001c0001t0021g0321 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1305+79G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108648526 | |||||||
| chr12:108648548 | T | C | 3 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02055.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1305+57A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108648548 | |||||||
| chr12:108648578 | G | T | 3 | a0001c0001t0002g0098 a0001c0001t0002g0102 a0001c0001t0002g0118 |
3 | HG00733.hp1 HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1305+27C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 10/10 | chr12 | 108648578 | |||||||
| chr12:108648932 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1059+31T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 9/10 | chr12 | 108648932 | |||||||
| chr12:108649150 | C | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1002-130G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108649150 | |||||||
| chr12:108649852 | G | C | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1002-832C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108649852 | |||||||
| chr12:108650180 | C | CT | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
160 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1002-1161dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650180 | |||||||
| chr12:108650180 | C | CTT | 48 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0026 others(45): Show |
48 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1002-1162_1002-116 others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650180 | |||||||
| chr12:108650180 | CT | C | 31 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0141 others(28): Show |
31 | HG00099.hp2 HG01255.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.1002-1161delA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650180 | |||||||
| chr12:108650180 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1002-1171_1002-116 others(15): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650180 | |||||||
| chr12:108650180 | CTTTTTTT others(9): Show |
C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1002-1176_1002-116 others(20): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650180 | |||||||
| chr12:108650778 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1001+1494G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650778 | |||||||
| chr12:108650869 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1001+1403A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650869 | |||||||
| chr12:108650947 | G | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1001+1325C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650947 | |||||||
| chr12:108650967 | T | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1001+1305A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108650967 | |||||||
| chr12:108651114 | G | A | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1001+1158C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108651114 | |||||||
| chr12:108651271 | T | C | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001+1001A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108651271 | |||||||
| chr12:108651352 | A | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1001+920T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108651352 | |||||||
| chr12:108651370 | G | A | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+902C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108651370 | |||||||
| chr12:108651578 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1001+694A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108651578 | |||||||
| chr12:108652041 | GA | G | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1001+230delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108652041 | |||||||
| chr12:108652055 | C | CT | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1001+216dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108652055 | |||||||
| chr12:108652055 | C | CTTTTT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1001+212_1001+216d others(7): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108652055 | |||||||
| chr12:108652055 | C | CTTTTTT | 75 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(72): Show |
75 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1001+211_1001+216d others(8): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 8/10 | chr12 | 108652055 | |||||||
| chr12:108652519 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.856-102G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652519 | |||||||
| chr12:108652845 | T | TCACAGAC others(12): Show |
263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.856-429_856-428ins others(19): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652845 | |||||||
| chr12:108652848 | G | A | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.856-431C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652848 | |||||||
| chr12:108652852 | G | GGCACTGA | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.856-436_856-435ins others(7): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652852 | |||||||
| chr12:108652853 | T | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.856-436A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652853 | |||||||
| chr12:108652908 | C | G | 1 | a0001c0001t0001g0025 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.856-491G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108652908 | |||||||
| chr12:108653278 | A | G | 6 | a0001c0001t0003g0278 a0001c0001t0003g0280 a0001c0001t0003g0281 others(3): Show |
6 | HG01109.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-861T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108653278 | |||||||
| chr12:108653821 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.855+485A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108653821 | |||||||
| chr12:108653943 | A | G | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.855+363T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108653943 | |||||||
| chr12:108653957 | A | G | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+349T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108653957 | |||||||
| chr12:108653965 | T | C | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.855+341A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108653965 | |||||||
| chr12:108654133 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.855+173T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108654133 | |||||||
| chr12:108654232 | C | T | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.855+74G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108654232 | |||||||
| chr12:108654271 | A | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.855+35T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 7/10 | chr12 | 108654271 | |||||||
| chr12:108654461 | A | T | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-51T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108654461 | |||||||
| chr12:108654637 | C | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.751-227G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108654637 | |||||||
| chr12:108654907 | T | C | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.751-497A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108654907 | |||||||
| chr12:108654966 | A | G | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.751-556T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108654966 | |||||||
| chr12:108655003 | C | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.751-593G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655003 | |||||||
| chr12:108655097 | T | TATTC | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.751-688_751-687ins others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655097 | |||||||
| chr12:108655119 | G | A | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.751-709C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655119 | |||||||
| chr12:108655369 | C | G | 1 | a0001c0001t0004g0296 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.751-959G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655369 | |||||||
| chr12:108655433 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1023G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655433 | |||||||
| chr12:108655439 | G | A | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.751-1029C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655439 | |||||||
| chr12:108655531 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.751-1121G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655531 | |||||||
| chr12:108655570 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.751-1160G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655570 | |||||||
| chr12:108655578 | C | T | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.751-1168G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655578 | |||||||
| chr12:108655590 | G | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.751-1180C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655590 | |||||||
| chr12:108655591 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0009g0267 |
2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.751-1181C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655591 | |||||||
| chr12:108655670 | G | A | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-1260C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655670 | |||||||
| chr12:108655695 | G | A | 58 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(55): Show |
62 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.751-1285C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655695 | |||||||
| chr12:108655721 | G | A | 54 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(51): Show |
58 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.751-1311C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655721 | |||||||
| chr12:108655723 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1313G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655723 | |||||||
| chr12:108655804 | TGTCTGGG others(32): Show |
T | 1 | a0001c0001t0002g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.751-1433_751-1395d others(41): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655804 | |||||||
| chr12:108655837 | G | A | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.751-1427C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655837 | |||||||
| chr12:108655852 | T | TGTGAGGA others(30): Show |
1 | a0001c0001t0001g0029 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.750+1415_751-1443d others(39): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655852 | |||||||
| chr12:108655899 | G | T | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1405C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655899 | |||||||
| chr12:108655959 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+1345G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108655959 | |||||||
| chr12:108656032 | A | AC | 4 | a0001c0001t0001g0077 a0001c0001t0003g0256 a0001c0001t0003g0315 others(1): Show |
4 | HG01192.hp2 HG01261.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1271dupG | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656032 | |||||||
| chr12:108656074 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.750+1230C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656074 | |||||||
| chr12:108656097 | T | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.750+1207A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656097 | |||||||
| chr12:108656108 | C | T | 6 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0200 others(3): Show |
6 | HG00423.hp1 HG00621.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.750+1196G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656108 | |||||||
| chr12:108656114 | G | A | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.750+1190C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656114 | |||||||
| chr12:108656138 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.750+1166T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656138 | |||||||
| chr12:108656178 | G | A | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
254 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.750+1126C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656178 | |||||||
| chr12:108656191 | C | G | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.750+1113G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656191 | |||||||
| chr12:108656194 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.750+1110C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656194 | |||||||
| chr12:108656222 | G | A | 9 | a0001c0001t0001g0092 a0001c0001t0002g0079 a0001c0001t0002g0085 others(6): Show |
9 | NA18947.hp2 NA18948.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.750+1082C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656222 | |||||||
| chr12:108656273 | C | T | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.750+1031G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656273 | |||||||
| chr12:108656294 | CTCAGCCC others(40): Show |
C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
191 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.750+963_750+1009de others(48): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656294 | |||||||
| chr12:108656304 | GCCCGGCC others(40): Show |
G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.750+953_750+999del others(47): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656304 | |||||||
| chr12:108656322 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.750+982A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656322 | |||||||
| chr12:108656372 | G | A | 8 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0004g0263 others(5): Show |
8 | HG00733.hp2 HG01192.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.750+932C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656372 | |||||||
| chr12:108656401 | C | G | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.750+903G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656401 | |||||||
| chr12:108656419 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.750+885C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656419 | |||||||
| chr12:108656428 | G | A | 74 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(71): Show |
75 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.750+876C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656428 | |||||||
| chr12:108656429 | T | G | 1 | a0001c0001t0001g0017 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.750+875A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656429 | |||||||
| chr12:108656431 | G | T | 1 | a0001c0001t0001g0017 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.750+873C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656431 | |||||||
| chr12:108656456 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.750+848T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656456 | |||||||
| chr12:108656478 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0169 |
2 | NA18940.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.750+826G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656478 | |||||||
| chr12:108656572 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.750+732C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656572 | |||||||
| chr12:108656585 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.750+719C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656585 | |||||||
| chr12:108656832 | A | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.750+472T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108656832 | |||||||
| chr12:108657057 | T | TA | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.750+246dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108657057 | |||||||
| chr12:108657066 | T | A | 1 | a0001c0001t0008g0319 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.750+238A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108657066 | |||||||
| chr12:108657067 | T | A | 1 | a0001c0002t0003g0285 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.750+237A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108657067 | |||||||
| chr12:108657075 | T | A | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.750+229A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108657075 | |||||||
| chr12:108657192 | C | T | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.750+112G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 6/10 | chr12 | 108657192 | |||||||
| chr12:108657676 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.631-253G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108657676 | |||||||
| chr12:108657806 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.631-383C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108657806 | |||||||
| chr12:108657848 | A | C | 1 | a0001c0001t0003g0260 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.631-425T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108657848 | |||||||
| chr12:108657897 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.631-474C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108657897 | |||||||
| chr12:108658167 | T | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
254 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.630+571A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658167 | |||||||
| chr12:108658253 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.630+485G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658253 | |||||||
| chr12:108658496 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.630+242T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658496 | |||||||
| chr12:108658554 | T | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.630+184A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658554 | |||||||
| chr12:108658581 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.630+157C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658581 | |||||||
| chr12:108658658 | C | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.630+80G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 5/10 | chr12 | 108658658 | |||||||
| chr12:108659213 | A | C | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.449-294T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659213 | |||||||
| chr12:108659216 | CAAAG | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0036 others(3): Show |
6 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.449-301_449-298del others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659216 | |||||||
| chr12:108659361 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG01167.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.449-442C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659361 | |||||||
| chr12:108659436 | T | A | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.449-517A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659436 | |||||||
| chr12:108659486 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.449-567A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659486 | |||||||
| chr12:108659561 | T | G | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.449-642A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659561 | |||||||
| chr12:108659595 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.449-676C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659595 | |||||||
| chr12:108659762 | G | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449-843C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659762 | |||||||
| chr12:108659852 | T | G | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.449-933A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108659852 | |||||||
| chr12:108660086 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.449-1167G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660086 | |||||||
| chr12:108660356 | C | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.449-1437G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660356 | |||||||
| chr12:108660389 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.449-1470A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660389 | |||||||
| chr12:108660451 | CA | C | 26 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0043 others(23): Show |
26 | HG00438.hp2 HG00673.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.449-1533delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660451 | |||||||
| chr12:108660451 | CAA | C | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
159 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.449-1534_449-1533d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660451 | |||||||
| chr12:108660451 | CAAA | C | 73 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0123 others(70): Show |
77 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.449-1535_449-1533d others(5): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660451 | |||||||
| chr12:108660634 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.448+1395C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660634 | |||||||
| chr12:108660699 | G | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.448+1330C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660699 | |||||||
| chr12:108660758 | G | C | 2 | a0001c0001t0001g0261 a0004c0004t0014g0134 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.448+1271C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660758 | |||||||
| chr12:108660847 | A | G | 19 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.448+1182T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660847 | |||||||
| chr12:108660973 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.448+1056A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108660973 | |||||||
| chr12:108661237 | T | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.448+792A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661237 | |||||||
| chr12:108661265 | G | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.448+764C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661265 | |||||||
| chr12:108661329 | G | T | 1 | a0001c0001t0002g0100 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.448+700C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661329 | |||||||
| chr12:108661461 | G | A | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.448+568C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661461 | |||||||
| chr12:108661528 | A | C | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.448+501T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661528 | |||||||
| chr12:108661555 | T | C | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.448+474A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661555 | |||||||
| chr12:108661596 | G | GA | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.448+432dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661596 | |||||||
| chr12:108661668 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.448+361G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661668 | |||||||
| chr12:108661845 | G | A | 1 | a0001c0001t0005g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.448+184C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661845 | |||||||
| chr12:108661888 | C | T | 3 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 |
3 | HG01243.hp1 HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.448+141G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 4/10 | chr12 | 108661888 | |||||||
| chr12:108662189 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.319-31A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662189 | |||||||
| chr12:108662317 | G | GT | 18 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0137 others(15): Show |
18 | HG01099.hp2 HG01433.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.319-160dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662317 | |||||||
| chr12:108662324 | T | TG | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.319-167_319-166ins others(1): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662324 | |||||||
| chr12:108662365 | G | A | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-207C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662365 | |||||||
| chr12:108662405 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-247C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662405 | |||||||
| chr12:108662494 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.319-336T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662494 | |||||||
| chr12:108662601 | T | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.319-443A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662601 | |||||||
| chr12:108662648 | T | C | 1 | a0001c0001t0006g0148 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.319-490A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662648 | |||||||
| chr12:108662916 | C | A | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.319-758G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662916 | |||||||
| chr12:108662937 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.319-779C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108662937 | |||||||
| chr12:108663022 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.319-864A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663022 | |||||||
| chr12:108663207 | A | G | 7 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0083 others(4): Show |
7 | HG00438.hp1 NA18957.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-1049T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663207 | |||||||
| chr12:108663255 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.319-1097G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663255 | |||||||
| chr12:108663261 | A | T | 67 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(64): Show |
68 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.319-1103T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663261 | |||||||
| chr12:108663310 | C | T | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.319-1152G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663310 | |||||||
| chr12:108663608 | T | C | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-1450A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663608 | |||||||
| chr12:108663634 | T | C | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-1476A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663634 | |||||||
| chr12:108663673 | T | C | 53 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0140 others(50): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.319-1515A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108663673 | |||||||
| chr12:108664033 | A | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
248 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.319-1875T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108664033 | |||||||
| chr12:108664124 | TAA | T | 3 | a0001c0002t0003g0284 a0001c0002t0003g0287 a0001c0002t0003g0288 |
3 | HG02109.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.319-1968_319-1967d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108664124 | |||||||
| chr12:108664381 | T | G | 1 | a0001c0001t0002g0125 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.319-2223A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108664381 | |||||||
| chr12:108664752 | T | C | 1 | a0001c0001t0006g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-2594A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108664752 | |||||||
| chr12:108665208 | T | C | 1 | a0001c0001t0002g0115 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.319-3050A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665208 | |||||||
| chr12:108665374 | T | G | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-3216A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665374 | |||||||
| chr12:108665562 | CAGTT | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
53 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.319-3408_319-3405d others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665562 | |||||||
| chr12:108665673 | A | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.319-3515T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665673 | |||||||
| chr12:108665848 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.319-3690C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665848 | |||||||
| chr12:108665864 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.319-3706G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108665864 | |||||||
| chr12:108666017 | G | T | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-3859C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666017 | |||||||
| chr12:108666088 | C | T | 3 | a0001c0001t0004g0270 a0001c0001t0004g0299 a0001c0001t0018g0271 |
3 | HG03130.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.319-3930G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666088 | |||||||
| chr12:108666126 | G | C | 1 | a0001c0001t0003g0256 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.319-3968C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666126 | |||||||
| chr12:108666524 | G | C | 3 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02071.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.319-4366C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666524 | |||||||
| chr12:108666850 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.319-4692G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666850 | |||||||
| chr12:108666963 | G | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.319-4805C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108666963 | |||||||
| chr12:108667009 | A | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-4851T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667009 | |||||||
| chr12:108667072 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.319-4914C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667072 | |||||||
| chr12:108667330 | G | T | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.319-5172C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667330 | |||||||
| chr12:108667349 | T | G | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-5191A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667349 | |||||||
| chr12:108667402 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319-5244A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667402 | |||||||
| chr12:108667414 | A | T | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-5256T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667414 | |||||||
| chr12:108667489 | T | A | 1 | a0001c0001t0003g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.319-5331A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667489 | |||||||
| chr12:108667550 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.319-5392G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667550 | |||||||
| chr12:108667658 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.319-5500C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667658 | |||||||
| chr12:108667755 | T | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-5597A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667755 | |||||||
| chr12:108667927 | C | T | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-5769G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667927 | |||||||
| chr12:108667928 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.319-5770C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667928 | |||||||
| chr12:108667957 | T | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-5799A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667957 | |||||||
| chr12:108667988 | C | T | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-5830G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108667988 | |||||||
| chr12:108668015 | C | G | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-5857G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668015 | |||||||
| chr12:108668265 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.319-6107C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668265 | |||||||
| chr12:108668301 | G | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.319-6143C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668301 | |||||||
| chr12:108668422 | T | C | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-6264A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668422 | |||||||
| chr12:108668645 | T | C | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-6487A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668645 | |||||||
| chr12:108668690 | A | G | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-6532T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668690 | |||||||
| chr12:108668905 | T | C | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-6747A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668905 | |||||||
| chr12:108668992 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.319-6834A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108668992 | |||||||
| chr12:108669062 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0178 |
2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.319-6904G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669062 | |||||||
| chr12:108669182 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02071.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.319-7024C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669182 | |||||||
| chr12:108669312 | T | A | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.319-7154A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669312 | |||||||
| chr12:108669429 | G | A | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-7271C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669429 | |||||||
| chr12:108669463 | T | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
57 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.319-7305A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669463 | |||||||
| chr12:108669500 | G | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-7342C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669500 | |||||||
| chr12:108669673 | T | TA | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
166 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.319-7516dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669673 | |||||||
| chr12:108669673 | TA | T | 9 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(6): Show |
9 | HG01109.hp1 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-7516delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108669673 | |||||||
| chr12:108670068 | T | G | 11 | a0001c0001t0001g0168 a0001c0001t0001g0268 a0001c0001t0001g0269 others(8): Show |
11 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.319-7910A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108670068 | |||||||
| chr12:108670182 | A | G | 57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.319-8024T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108670182 | |||||||
| chr12:108670816 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0056 |
2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.318+7456C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108670816 | |||||||
| chr12:108671119 | G | A | 1 | a0001c0006t0003g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.318+7153C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671119 | |||||||
| chr12:108671164 | G | A | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7108C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671164 | |||||||
| chr12:108671171 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+7101G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671171 | |||||||
| chr12:108671385 | A | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+6887T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671385 | |||||||
| chr12:108671465 | G | GA | 53 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(50): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.318+6806dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671465 | |||||||
| chr12:108671681 | T | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+6591A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671681 | |||||||
| chr12:108671700 | C | T | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+6572G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671700 | |||||||
| chr12:108671800 | T | C | 14 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(11): Show |
14 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.318+6472A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671800 | |||||||
| chr12:108671822 | G | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.318+6450C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108671822 | |||||||
| chr12:108672036 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.318+6236A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672036 | |||||||
| chr12:108672072 | A | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.318+6200T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672072 | |||||||
| chr12:108672165 | A | G | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+6107T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672165 | |||||||
| chr12:108672221 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.318+6051G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672221 | |||||||
| chr12:108672539 | G | A | 1 | a0001c0001t0003g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.318+5733C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672539 | |||||||
| chr12:108672657 | GT | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+5614delA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672657 | |||||||
| chr12:108672668 | T | A | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.318+5604A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108672668 | |||||||
| chr12:108673016 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0177 others(2): Show |
5 | HG02602.hp2 HG02683.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+5256G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108673016 | |||||||
| chr12:108673018 | C | T | 5 | a0001c0002t0003g0284 a0001c0002t0003g0285 a0001c0002t0003g0287 others(2): Show |
5 | HG01433.hp1 HG02109.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+5254G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108673018 | |||||||
| chr12:108673099 | T | C | 1 | a0001c0001t0004g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+5173A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108673099 | |||||||
| chr12:108673845 | T | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+4427A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108673845 | |||||||
| chr12:108673892 | AAAAT | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+4376_318+4379d others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108673892 | |||||||
| chr12:108674086 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.318+4186G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674086 | |||||||
| chr12:108674121 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.318+4151C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674121 | |||||||
| chr12:108674191 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.318+4081A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674191 | |||||||
| chr12:108674328 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.318+3944G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674328 | |||||||
| chr12:108674434 | G | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+3838C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674434 | |||||||
| chr12:108674441 | G | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+3831C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674441 | |||||||
| chr12:108674443 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.318+3829T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674443 | |||||||
| chr12:108674444 | G | A | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.318+3828C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674444 | |||||||
| chr12:108674527 | G | A | 54 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(51): Show |
58 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.318+3745C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674527 | |||||||
| chr12:108674552 | T | TA | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.318+3719dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674552 | |||||||
| chr12:108674552 | TA | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.318+3719delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674552 | |||||||
| chr12:108674552 | TAA | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+3718_318+3719d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674552 | |||||||
| chr12:108674638 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.318+3634A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674638 | |||||||
| chr12:108674867 | A | C | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3405T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108674867 | |||||||
| chr12:108675051 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.318+3221A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675051 | |||||||
| chr12:108675180 | G | GTA | 5 | a0001c0001t0001g0037 a0001c0001t0001g0214 a0001c0001t0002g0053 others(2): Show |
5 | HG01255.hp1 HG02523.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3090_318+3091d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675180 | |||||||
| chr12:108675230 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+3042G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675230 | |||||||
| chr12:108675241 | A | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.318+3031T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675241 | |||||||
| chr12:108675709 | C | A | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.318+2563G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675709 | |||||||
| chr12:108675805 | G | A | 10 | a0001c0001t0001g0139 a0001c0001t0001g0170 a0001c0001t0001g0174 others(7): Show |
10 | HG02523.hp2 HG02602.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+2467C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675805 | |||||||
| chr12:108675924 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
252 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.318+2348G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108675924 | |||||||
| chr12:108676047 | A | C | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+2225T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676047 | |||||||
| chr12:108676130 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.318+2142G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676130 | |||||||
| chr12:108676353 | T | C | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.318+1919A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676353 | |||||||
| chr12:108676605 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.318+1667G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676605 | |||||||
| chr12:108676740 | C | T | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1532G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676740 | |||||||
| chr12:108676771 | C | CA | 87 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(84): Show |
88 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.318+1500dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676771 | |||||||
| chr12:108676837 | C | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+1435G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676837 | |||||||
| chr12:108676979 | GAAAAGCG others(3): Show |
G | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.318+1283_318+1292d others(12): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108676979 | |||||||
| chr12:108677118 | C | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
53 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.318+1154G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677118 | |||||||
| chr12:108677183 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(31): Show |
34 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(31): Show |
intron_variant | MODIFIER | c.318+1089G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677183 | |||||||
| chr12:108677364 | C | T | 1 | a0001c0001t0004g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.318+908G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677364 | |||||||
| chr12:108677367 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0065 |
3 | HG01081.hp2 HG01358.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.318+905G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677367 | |||||||
| chr12:108677476 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.318+796G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677476 | |||||||
| chr12:108677572 | G | A | 2 | a0001c0001t0015g0131 a0001c0001t0021g0321 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.318+700C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677572 | |||||||
| chr12:108677610 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0049 others(3): Show |
6 | NA18957.hp1 NA18959.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+662A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677610 | |||||||
| chr12:108677792 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.318+480C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677792 | |||||||
| chr12:108677900 | T | A | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.318+372A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677900 | |||||||
| chr12:108677909 | C | T | 53 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(50): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.318+363G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108677909 | |||||||
| chr12:108678018 | C | CA | 55 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(52): Show |
55 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.318+253dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108678018 | |||||||
| chr12:108678046 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.318+226C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108678046 | |||||||
| chr12:108678083 | T | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+189A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108678083 | |||||||
| chr12:108678099 | C | CTGTA | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0141 others(7): Show |
10 | HG00423.hp2 NA18960.hp1 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.318+169_318+172dup others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108678099 | |||||||
| chr12:108678184 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.318+88T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 3/10 | chr12 | 108678184 | |||||||
| chr12:108678443 | C | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.196-49G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678443 | |||||||
| chr12:108678507 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.196-113C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678507 | |||||||
| chr12:108678699 | A | G | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196-305T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678699 | |||||||
| chr12:108678713 | T | C | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-319A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678713 | |||||||
| chr12:108678718 | T | TA | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
68 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.196-325dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678718 | |||||||
| chr12:108678718 | TA | T | 56 | a0001c0001t0001g0017 a0001c0001t0001g0039 a0001c0001t0001g0042 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.196-325delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678718 | |||||||
| chr12:108678718 | TAA | T | 6 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-326_196-325del others(2): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678718 | |||||||
| chr12:108678773 | A | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.196-379T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678773 | |||||||
| chr12:108678895 | G | A | 2 | a0001c0001t0003g0286 a0001c0001t0003g0290 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.196-501C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678895 | |||||||
| chr12:108678972 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.196-578C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108678972 | |||||||
| chr12:108679066 | G | A | 2 | a0001c0001t0004g0270 a0001c0001t0018g0271 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.196-672C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679066 | |||||||
| chr12:108679109 | C | CA | 21 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0076 others(18): Show |
21 | HG00621.hp2 HG01433.hp1 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-716dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679109 | |||||||
| chr12:108679109 | CA | C | 26 | a0001c0001t0001g0017 a0001c0001t0001g0144 a0001c0001t0001g0145 others(23): Show |
26 | HG00140.hp2 HG00733.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-716delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679109 | |||||||
| chr12:108679125 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.196-731T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679125 | |||||||
| chr12:108679126 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196-732T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679126 | |||||||
| chr12:108679144 | GA | G | 10 | a0001c0001t0003g0278 a0001c0001t0003g0283 a0001c0001t0003g0286 others(7): Show |
10 | HG01433.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-751delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679144 | |||||||
| chr12:108679170 | T | TA | 23 | a0001c0001t0001g0076 a0001c0001t0003g0238 a0001c0001t0003g0239 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.196-777dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679170 | |||||||
| chr12:108679170 | TA | T | 10 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0143 others(7): Show |
10 | HG01081.hp1 HG01169.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-777delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679170 | |||||||
| chr12:108679455 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.196-1061C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679455 | |||||||
| chr12:108679552 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-1158G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679552 | |||||||
| chr12:108679562 | C | T | 55 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(52): Show |
59 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.196-1168G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679562 | |||||||
| chr12:108679868 | T | C | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-1474A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108679868 | |||||||
| chr12:108680268 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.196-1874A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680268 | |||||||
| chr12:108680279 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.196-1885A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680279 | |||||||
| chr12:108680396 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.196-2002T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680396 | |||||||
| chr12:108680482 | C | T | 2 | a0001c0001t0003g0286 a0001c0001t0003g0290 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.196-2088G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680482 | |||||||
| chr12:108680533 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.196-2139A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680533 | |||||||
| chr12:108680584 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-2190G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680584 | |||||||
| chr12:108680671 | T | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.196-2277A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108680671 | |||||||
| chr12:108681129 | T | C | 17 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.196-2735A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108681129 | |||||||
| chr12:108681367 | T | A | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196-2973A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108681367 | |||||||
| chr12:108681407 | T | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
57 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.196-3013A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108681407 | |||||||
| chr12:108681581 | C | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.196-3187G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108681581 | |||||||
| chr12:108681683 | T | C | 3 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0243 |
3 | HG01069.hp2 HG01071.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.196-3289A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108681683 | |||||||
| chr12:108682049 | G | T | 1 | a0001c0001t0003g0254 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.196-3655C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108682049 | |||||||
| chr12:108682369 | C | T | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196-3975G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108682369 | |||||||
| chr12:108682479 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196-4085G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108682479 | |||||||
| chr12:108682515 | T | C | 13 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0186 others(10): Show |
13 | HG00423.hp1 HG00621.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-4121A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108682515 | |||||||
| chr12:108682549 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.196-4155G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108682549 | |||||||
| chr12:108683019 | A | C | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-4625T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683019 | |||||||
| chr12:108683235 | T | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.196-4841A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683235 | |||||||
| chr12:108683396 | G | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.196-5002C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683396 | |||||||
| chr12:108683418 | C | CA | 56 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(53): Show |
56 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.196-5025dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683418 | |||||||
| chr12:108683418 | CA | C | 15 | a0001c0001t0001g0048 a0001c0001t0001g0191 a0001c0001t0001g0268 others(12): Show |
15 | HG01070.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-5025delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683418 | |||||||
| chr12:108683459 | A | AAAAATAA others(5): Show |
57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.196-5077_196-5066d others(14): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683459 | |||||||
| chr12:108683459 | A | AAAAATAA others(5): Show |
191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.196-5066_196-5065i others(14): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683459 | |||||||
| chr12:108683741 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0059 |
2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.196-5347G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683741 | |||||||
| chr12:108683747 | C | A | 1 | a0001c0001t0001g0032 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.196-5353G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683747 | |||||||
| chr12:108683765 | A | T | 2 | a0001c0001t0003g0256 a0001c0001t0008g0255 |
2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.196-5371T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683765 | |||||||
| chr12:108683894 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196-5500A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683894 | |||||||
| chr12:108683946 | TTGAAGCC others(6): Show |
T | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196-5565_196-5553d others(15): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108683946 | |||||||
| chr12:108684111 | A | G | 3 | a0001c0001t0002g0089 a0001c0001t0002g0096 a0001c0001t0002g0120 |
3 | HG00673.hp2 NA18964.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.196-5717T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684111 | |||||||
| chr12:108684139 | A | G | 57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.196-5745T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684139 | |||||||
| chr12:108684208 | T | C | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.196-5814A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684208 | |||||||
| chr12:108684286 | A | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.196-5892T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684286 | |||||||
| chr12:108684293 | A | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.196-5899T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684293 | |||||||
| chr12:108684566 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0038 |
2 | NA19055.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.196-6172G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684566 | |||||||
| chr12:108684678 | C | T | 1 | a0001c0001t0007g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196-6284G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684678 | |||||||
| chr12:108684691 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196-6297C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108684691 | |||||||
| chr12:108685126 | A | T | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-6732T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108685126 | |||||||
| chr12:108685295 | TACTAGAG others(16): Show |
T | 1 | a0001c0001t0001g0017 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.196-6924_196-6902d others(25): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108685295 | |||||||
| chr12:108685671 | C | CAG | 57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.196-7279_196-7278d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108685671 | |||||||
| chr12:108686254 | C | T | 57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.196-7860G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686254 | |||||||
| chr12:108686299 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0065 |
3 | HG01081.hp2 HG01358.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.196-7905G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686299 | |||||||
| chr12:108686329 | T | C | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-7935A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686329 | |||||||
| chr12:108686353 | C | T | 1 | a0001c0001t0016g0279 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196-7959G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686353 | |||||||
| chr12:108686496 | A | T | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196-8102T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686496 | |||||||
| chr12:108686554 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.196-8160T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686554 | |||||||
| chr12:108686653 | T | C | 1 | a0001c0001t0001g0014 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.196-8259A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686653 | |||||||
| chr12:108686791 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-8397A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686791 | |||||||
| chr12:108686869 | G | A | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-8475C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686869 | |||||||
| chr12:108686892 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.196-8498C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686892 | |||||||
| chr12:108686944 | G | C | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196-8550C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686944 | |||||||
| chr12:108686945 | C | G | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196-8551G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108686945 | |||||||
| chr12:108687094 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0031 |
2 | NA18999.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.196-8700C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687094 | |||||||
| chr12:108687358 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.196-8964C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687358 | |||||||
| chr12:108687409 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.196-9015G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687409 | |||||||
| chr12:108687444 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.196-9050C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687444 | |||||||
| chr12:108687555 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.196-9161G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687555 | |||||||
| chr12:108687560 | G | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.196-9166C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687560 | |||||||
| chr12:108687660 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.196-9266G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687660 | |||||||
| chr12:108687747 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.196-9353A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687747 | |||||||
| chr12:108687757 | C | G | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196-9363G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687757 | |||||||
| chr12:108687760 | G | A | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196-9366C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687760 | |||||||
| chr12:108687804 | A | G | 5 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(2): Show |
5 | HG02717.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-9410T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687804 | |||||||
| chr12:108687841 | G | A | 1 | a0001c0001t0002g0016 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.196-9447C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687841 | |||||||
| chr12:108687924 | C | CT | 79 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(76): Show |
80 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.196-9531dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687924 | |||||||
| chr12:108687924 | C | CTT | 11 | a0001c0001t0001g0036 a0001c0001t0001g0261 a0001c0001t0004g0263 others(8): Show |
11 | HG00597.hp2 HG02055.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-9532_196-9531d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108687924 | |||||||
| chr12:108688201 | G | A | 1 | a0001c0001t0003g0314 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.196-9807C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688201 | |||||||
| chr12:108688295 | C | A | 1 | a0001c0001t0001g0032 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.196-9901G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688295 | |||||||
| chr12:108688422 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196-10028A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688422 | |||||||
| chr12:108688467 | T | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.196-10073A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688467 | |||||||
| chr12:108688507 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.196-10113C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688507 | |||||||
| chr12:108688689 | C | G | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.196-10295G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688689 | |||||||
| chr12:108688703 | T | A | 5 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(2): Show |
5 | HG02717.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-10309A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688703 | |||||||
| chr12:108688843 | A | C | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.196-10449T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688843 | |||||||
| chr12:108688849 | G | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.196-10455C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688849 | |||||||
| chr12:108688914 | C | T | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-10520G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688914 | |||||||
| chr12:108688946 | G | T | 19 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(16): Show |
19 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-10552C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108688946 | |||||||
| chr12:108689032 | G | GA | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.196-10639dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689032 | |||||||
| chr12:108689056 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196-10662G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689056 | |||||||
| chr12:108689104 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.196-10710C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689104 | |||||||
| chr12:108689186 | C | A | 1 | a0001c0001t0001g0072 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.196-10792G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689186 | |||||||
| chr12:108689223 | C | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.196-10829G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689223 | |||||||
| chr12:108689292 | C | G | 1 | a0001c0001t0008g0255 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.196-10898G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689292 | |||||||
| chr12:108689351 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196-10957T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689351 | |||||||
| chr12:108689352 | T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.196-10958A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689352 | |||||||
| chr12:108689370 | C | T | 5 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(2): Show |
5 | HG02717.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-10976G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689370 | |||||||
| chr12:108689624 | C | T | 6 | a0001c0001t0001g0123 a0001c0001t0002g0080 a0001c0001t0002g0094 others(3): Show |
6 | HG02071.hp2 NA18959.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-11230G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689624 | |||||||
| chr12:108689776 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0215 |
2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.195+11348C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108689776 | |||||||
| chr12:108690023 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.195+11101C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108690023 | |||||||
| chr12:108690064 | G | C | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+11060C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108690064 | |||||||
| chr12:108690065 | C | G | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+11059G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108690065 | |||||||
| chr12:108690082 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.195+11042C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108690082 | |||||||
| chr12:108690285 | AAAAGGAG others(3): Show |
A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+10829_195+1083 others(14): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108690285 | |||||||
| chr12:108691027 | T | C | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.195+10097A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691027 | |||||||
| chr12:108691042 | C | T | 1 | a0001c0001t0007g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.195+10082G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691042 | |||||||
| chr12:108691053 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.195+10071C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691053 | |||||||
| chr12:108691072 | T | C | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+10052A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691072 | |||||||
| chr12:108691080 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.195+10044A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691080 | |||||||
| chr12:108691095 | T | G | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG01167.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+10029A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691095 | |||||||
| chr12:108691105 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.195+10019C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691105 | |||||||
| chr12:108691113 | A | G | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(74): Show |
78 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.195+10011T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691113 | |||||||
| chr12:108691200 | CA | C | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+9923delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691200 | |||||||
| chr12:108691259 | T | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.195+9865A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691259 | |||||||
| chr12:108691332 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0071 |
3 | NA18944.hp1 NA18970.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.195+9792C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691332 | |||||||
| chr12:108691607 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.195+9517T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691607 | |||||||
| chr12:108691609 | T | C | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+9515A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691609 | |||||||
| chr12:108691610 | C | T | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+9514G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691610 | |||||||
| chr12:108691634 | C | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+9490G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691634 | |||||||
| chr12:108691636 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.195+9488G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691636 | |||||||
| chr12:108691720 | A | C | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+9404T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108691720 | |||||||
| chr12:108692003 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0065 |
2 | HG01358.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.195+9121G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692003 | |||||||
| chr12:108692019 | T | A | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.195+9105A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692019 | |||||||
| chr12:108692086 | C | T | 6 | a0001c0001t0001g0123 a0001c0001t0002g0080 a0001c0001t0002g0094 others(3): Show |
6 | HG02071.hp2 NA18959.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+9038G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692086 | |||||||
| chr12:108692156 | G | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.195+8968C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692156 | |||||||
| chr12:108692649 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.195+8475C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692649 | |||||||
| chr12:108692793 | G | T | 1 | a0001c0001t0019g0101 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.195+8331C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692793 | |||||||
| chr12:108692794 | C | CT | 216 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.195+8329dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692794 | |||||||
| chr12:108692794 | C | CTT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0037 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.195+8328_195+8329d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692794 | |||||||
| chr12:108692847 | G | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.195+8277C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692847 | |||||||
| chr12:108692861 | T | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.195+8263A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692861 | |||||||
| chr12:108692922 | C | G | 2 | a0001c0001t0003g0253 a0001c0001t0003g0254 |
2 | HG00140.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.195+8202G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108692922 | |||||||
| chr12:108693050 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.195+8074C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693050 | |||||||
| chr12:108693078 | T | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.195+8046A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693078 | |||||||
| chr12:108693088 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18981.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.195+8036C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693088 | |||||||
| chr12:108693210 | T | C | 6 | a0001c0001t0003g0283 a0001c0002t0003g0284 a0001c0002t0003g0285 others(3): Show |
6 | HG01433.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+7914A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693210 | |||||||
| chr12:108693217 | T | C | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.195+7907A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693217 | |||||||
| chr12:108693263 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.195+7861T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693263 | |||||||
| chr12:108693327 | T | C | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+7797A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693327 | |||||||
| chr12:108693393 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0065 |
2 | HG01358.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.195+7731C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693393 | |||||||
| chr12:108693426 | C | G | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.195+7698G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693426 | |||||||
| chr12:108693569 | G | T | 2 | a0001c0001t0004g0294 a0001c0001t0004g0295 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.195+7555C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693569 | |||||||
| chr12:108693760 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.195+7364T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693760 | |||||||
| chr12:108693837 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.195+7287C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693837 | |||||||
| chr12:108693867 | C | T | 1 | a0001c0006t0003g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.195+7257G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693867 | |||||||
| chr12:108693868 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.195+7256G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693868 | |||||||
| chr12:108693869 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.195+7255C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693869 | |||||||
| chr12:108693961 | C | A | 1 | a0001c0001t0003g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.195+7163G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693961 | |||||||
| chr12:108693967 | G | T | 76 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(73): Show |
77 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.195+7157C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108693967 | |||||||
| chr12:108694033 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.195+7091C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694033 | |||||||
| chr12:108694139 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.195+6985C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694139 | |||||||
| chr12:108694159 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.195+6965C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694159 | |||||||
| chr12:108694279 | C | CA | 9 | a0001c0001t0003g0250 a0001c0001t0003g0254 a0001c0001t0003g0256 others(6): Show |
9 | HG00140.hp2 HG00738.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+6844dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694279 | |||||||
| chr12:108694279 | CA | C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0045 others(87): Show |
94 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.195+6844delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694279 | |||||||
| chr12:108694279 | CAA | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
114 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.195+6843_195+6844d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694279 | |||||||
| chr12:108694279 | CAAA | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.195+6842_195+6844d others(5): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694279 | |||||||
| chr12:108694320 | A | G | 5 | a0001c0001t0003g0272 a0001c0001t0003g0273 a0001c0001t0003g0274 others(2): Show |
5 | HG02717.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+6804T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694320 | |||||||
| chr12:108694431 | T | C | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.195+6693A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694431 | |||||||
| chr12:108694573 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02015.hp1 HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.195+6551G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694573 | |||||||
| chr12:108694776 | T | C | 6 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 others(3): Show |
6 | HG02055.hp2 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+6348A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694776 | |||||||
| chr12:108694792 | AT | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(313): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.195+6331delA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694792 | |||||||
| chr12:108694878 | T | C | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+6246A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108694878 | |||||||
| chr12:108695057 | G | A | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+6067C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695057 | |||||||
| chr12:108695131 | C | A | 1 | a0001c0001t0005g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.195+5993G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695131 | |||||||
| chr12:108695413 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0036 others(6): Show |
9 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+5711G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695413 | |||||||
| chr12:108695521 | C | T | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+5603G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695521 | |||||||
| chr12:108695566 | C | G | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+5558G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695566 | |||||||
| chr12:108695580 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.195+5544G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695580 | |||||||
| chr12:108695618 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(73): Show |
77 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.195+5506C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695618 | |||||||
| chr12:108695850 | C | CT | 4 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0002g0020 others(1): Show |
4 | NA18957.hp1 NA18966.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+5273dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695850 | |||||||
| chr12:108695851 | T | TA | 87 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0058 others(84): Show |
91 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.195+5272dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695851 | |||||||
| chr12:108695851 | T | TAA | 21 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(18): Show |
21 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+5271_195+5272d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695851 | |||||||
| chr12:108695851 | T | TAAAAAAA others(11): Show |
1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+5255_195+5272d others(20): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695851 | |||||||
| chr12:108695851 | T | TAAAAAAA others(23): Show |
1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.195+5272_195+5273i others(32): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695851 | |||||||
| chr12:108695851 | TA | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0171 others(3): Show |
6 | HG01256.hp1 HG02698.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+5272delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108695851 | |||||||
| chr12:108696263 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.195+4861G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696263 | |||||||
| chr12:108696352 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0198 |
2 | NA18964.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.195+4772G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696352 | |||||||
| chr12:108696413 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.195+4711C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696413 | |||||||
| chr12:108696569 | A | C | 1 | a0001c0001t0013g0132 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.195+4555T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696569 | |||||||
| chr12:108696610 | G | A | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+4514C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696610 | |||||||
| chr12:108696805 | G | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+4319C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696805 | |||||||
| chr12:108696813 | G | A | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+4311C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696813 | |||||||
| chr12:108696855 | C | G | 1 | a0001c0001t0012g0133 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.195+4269G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108696855 | |||||||
| chr12:108697313 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.195+3811A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108697313 | |||||||
| chr12:108697955 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.195+3169G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108697955 | |||||||
| chr12:108697959 | T | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0267 |
3 | HG01884.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.195+3165A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108697959 | |||||||
| chr12:108697996 | T | A | 6 | a0001c0001t0003g0283 a0001c0002t0003g0284 a0001c0002t0003g0285 others(3): Show |
6 | HG01433.hp1 HG02109.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+3128A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108697996 | |||||||
| chr12:108698233 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.195+2891T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698233 | |||||||
| chr12:108698243 | C | T | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.195+2881G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698243 | |||||||
| chr12:108698309 | T | C | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+2815A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698309 | |||||||
| chr12:108698627 | G | A | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.195+2497C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698627 | |||||||
| chr12:108698654 | G | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.195+2470C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698654 | |||||||
| chr12:108698864 | T | C | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+2260A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698864 | |||||||
| chr12:108698939 | G | T | 23 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.195+2185C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698939 | |||||||
| chr12:108698941 | C | T | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.195+2183G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108698941 | |||||||
| chr12:108699020 | C | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.195+2104G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699020 | |||||||
| chr12:108699120 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.195+2004T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699120 | |||||||
| chr12:108699303 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.195+1821A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699303 | |||||||
| chr12:108699533 | C | T | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+1591G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699533 | |||||||
| chr12:108699567 | G | A | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.195+1557C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699567 | |||||||
| chr12:108699812 | T | C | 7 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0242 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+1312A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699812 | |||||||
| chr12:108699937 | C | T | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.195+1187G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699937 | |||||||
| chr12:108699948 | A | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.195+1176T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108699948 | |||||||
| chr12:108700107 | TCCATTGT others(11): Show |
T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(18): Show |
21 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.195+999_195+1016de others(19): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108700107 | |||||||
| chr12:108700574 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG01167.hp1 HG01169.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.195+550G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108700574 | |||||||
| chr12:108700887 | TATA | T | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.195+234_195+236del others(3): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108700887 | |||||||
| chr12:108701014 | G | T | 1 | a0001c0001t0003g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.195+110C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108701014 | |||||||
| chr12:108701015 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.195+109T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108701015 | |||||||
| chr12:108701109 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.195+15C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 2/10 | chr12 | 108701109 | |||||||
| chr12:108701361 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(67): Show |
71 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-5-38T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108701361 | |||||||
| chr12:108701594 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-5-271A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108701594 | |||||||
| chr12:108701928 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-5-605G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108701928 | |||||||
| chr12:108702047 | G | T | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5-724C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702047 | |||||||
| chr12:108702171 | G | A | 23 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5-848C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702171 | |||||||
| chr12:108702212 | G | A | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5-889C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702212 | |||||||
| chr12:108702242 | T | C | 17 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5-919A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702242 | |||||||
| chr12:108702280 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-957C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702280 | |||||||
| chr12:108702606 | G | A | 1 | a0001c0002t0003g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-5-1283C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702606 | |||||||
| chr12:108702615 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-5-1292A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702615 | |||||||
| chr12:108702647 | T | C | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-1324A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702647 | |||||||
| chr12:108702720 | C | T | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5-1397G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702720 | |||||||
| chr12:108702826 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-5-1503G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702826 | |||||||
| chr12:108702923 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-5-1600A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108702923 | |||||||
| chr12:108703458 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0267 |
3 | HG01884.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-5-2135G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108703458 | |||||||
| chr12:108703481 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-5-2158T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108703481 | |||||||
| chr12:108703755 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-5-2432C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108703755 | |||||||
| chr12:108703761 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-5-2438T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108703761 | |||||||
| chr12:108703778 | C | CCCTGGA | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-5-2456_-5-2455ins others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108703778 | |||||||
| chr12:108704081 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-5-2758G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704081 | |||||||
| chr12:108704158 | G | A | 1 | a0001c0001t0006g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-5-2835C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704158 | |||||||
| chr12:108704424 | A | G | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-5-3101T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704424 | |||||||
| chr12:108704450 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(30): Show |
33 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5-3127G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704450 | |||||||
| chr12:108704471 | C | CA | 105 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0135 others(102): Show |
109 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-5-3149dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704471 | |||||||
| chr12:108704733 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0267 |
3 | HG01884.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-5-3410C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704733 | |||||||
| chr12:108704995 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-5-3672C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108704995 | |||||||
| chr12:108705231 | C | T | 1 | a0001c0001t0006g0148 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-5-3908G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705231 | |||||||
| chr12:108705399 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-5-4076C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705399 | |||||||
| chr12:108705408 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-5-4085G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705408 | |||||||
| chr12:108705431 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0156 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-5-4108C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705431 | |||||||
| chr12:108705435 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-5-4112T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705435 | |||||||
| chr12:108705459 | C | CA | 21 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0157 others(18): Show |
21 | HG01071.hp2 HG01169.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-5-4137dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705459 | |||||||
| chr12:108705459 | C | CAA | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-5-4138_-5-4137dup others(2): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705459 | |||||||
| chr12:108705459 | C | CAAA | 81 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(78): Show |
82 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-5-4139_-5-4137dup others(3): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705459 | |||||||
| chr12:108705459 | C | CAAAA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0035 others(4): Show |
7 | HG00597.hp2 HG00621.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-4140_-5-4137dup others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705459 | |||||||
| chr12:108705691 | C | G | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-4368G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705691 | |||||||
| chr12:108705802 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-5-4479A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705802 | |||||||
| chr12:108705816 | A | G | 2 | a0001c0001t0015g0131 a0001c0001t0021g0321 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-5-4493T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705816 | |||||||
| chr12:108705847 | A | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-4524T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705847 | |||||||
| chr12:108705998 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-5-4675T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108705998 | |||||||
| chr12:108706008 | G | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(77): Show |
81 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.-5-4685C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706008 | |||||||
| chr12:108706186 | C | CA | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-5-4864dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706186 | |||||||
| chr12:108706186 | C | CAA | 14 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0038 others(11): Show |
14 | HG00621.hp1 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-5-4865_-5-4864dup others(2): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706186 | |||||||
| chr12:108706196 | C | A | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
252 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.-5-4873G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706196 | |||||||
| chr12:108706197 | A | C | 3 | a0001c0001t0015g0131 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02886.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-5-4874T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706197 | |||||||
| chr12:108706205 | C | A | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0310 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-5-4882G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706205 | |||||||
| chr12:108706601 | A | T | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5-5278T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706601 | |||||||
| chr12:108706628 | T | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5-5305A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706628 | |||||||
| chr12:108706647 | C | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-5324G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706647 | |||||||
| chr12:108706727 | C | T | 79 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(76): Show |
80 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-5-5404G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706727 | |||||||
| chr12:108706732 | C | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-5-5409G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706732 | |||||||
| chr12:108706746 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG00140.hp1 HG01261.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-5423C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706746 | |||||||
| chr12:108706747 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0061 others(3): Show |
6 | HG00140.hp1 HG01261.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-5424G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706747 | |||||||
| chr12:108706804 | G | C | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-5-5481C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108706804 | |||||||
| chr12:108707526 | A | C | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-5-6203T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108707526 | |||||||
| chr12:108707729 | T | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-6406A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108707729 | |||||||
| chr12:108707852 | T | C | 2 | a0001c0001t0003g0286 a0001c0001t0003g0290 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-5-6529A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108707852 | |||||||
| chr12:108708007 | C | T | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-5-6684G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108708007 | |||||||
| chr12:108708319 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0187 a0001c0001t0001g0190 others(13): Show |
16 | HG00408.hp2 HG02165.hp1 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-5-6996T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108708319 | |||||||
| chr12:108708462 | G | GT | 16 | a0001c0001t0001g0158 a0001c0001t0001g0207 a0001c0001t0001g0230 others(13): Show |
16 | HG00597.hp1 HG00733.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-7140dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108708462 | |||||||
| chr12:108708590 | T | C | 2 | a0001c0001t0003g0291 a0001c0001t0003g0293 |
2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-7267A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108708590 | |||||||
| chr12:108708627 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-5-7304T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108708627 | |||||||
| chr12:108709023 | T | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(30): Show |
33 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5-7700A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709023 | |||||||
| chr12:108709032 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0069 |
2 | HG01346.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-5-7709C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709032 | |||||||
| chr12:108709119 | T | TTA | 3 | a0001c0001t0001g0218 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG02071.hp1 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-5-7798_-5-7797dup others(2): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709119 | |||||||
| chr12:108709141 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-7818C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709141 | |||||||
| chr12:108709207 | T | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.-5-7884A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709207 | |||||||
| chr12:108709358 | T | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-8035A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709358 | |||||||
| chr12:108709575 | T | A | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8252A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709575 | |||||||
| chr12:108709579 | C | A | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8256G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709579 | |||||||
| chr12:108709582 | T | TC | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8260_-5-8259ins others(1): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709582 | |||||||
| chr12:108709583 | T | C | 4 | a0001c0001t0001g0261 a0001c0001t0015g0131 a0001c0001t0021g0321 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-8260A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709583 | |||||||
| chr12:108709637 | C | A | 2 | a0001c0001t0015g0131 a0001c0001t0021g0321 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-5-8314G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709637 | |||||||
| chr12:108709839 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-5-8516T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709839 | |||||||
| chr12:108709897 | T | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-5-8574A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709897 | |||||||
| chr12:108709908 | G | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-8585C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108709908 | |||||||
| chr12:108710037 | A | G | 1 | a0001c0001t0004g0263 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-5-8714T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710037 | |||||||
| chr12:108710374 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-5-9051T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710374 | |||||||
| chr12:108710385 | C | G | 1 | a0001c0001t0002g0089 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-5-9062G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710385 | |||||||
| chr12:108710402 | A | T | 1 | a0001c0001t0003g0283 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-5-9079T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710402 | |||||||
| chr12:108710450 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-5-9127A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710450 | |||||||
| chr12:108710526 | C | T | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-5-9203G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710526 | |||||||
| chr12:108710622 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-5-9299A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710622 | |||||||
| chr12:108710712 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-5-9389A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710712 | |||||||
| chr12:108710883 | G | C | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-9560C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108710883 | |||||||
| chr12:108711066 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-5-9743A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711066 | |||||||
| chr12:108711100 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-5-9777A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711100 | |||||||
| chr12:108711161 | G | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-9838C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711161 | |||||||
| chr12:108711193 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-5-9870A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711193 | |||||||
| chr12:108711249 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-5-9926C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711249 | |||||||
| chr12:108711453 | G | A | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-10130C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711453 | |||||||
| chr12:108711679 | C | CA | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0224 others(4): Show |
7 | HG03098.hp2 HG03130.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.-5-10357dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711679 | |||||||
| chr12:108711725 | G | A | 3 | a0001c0001t0003g0242 a0001c0001t0003g0246 a0001c0001t0003g0247 |
3 | HG00735.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-5-10402C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711725 | |||||||
| chr12:108711771 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-5-10448A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711771 | |||||||
| chr12:108711780 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-5-10457G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711780 | |||||||
| chr12:108711897 | T | G | 3 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02055.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-5-10574A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108711897 | |||||||
| chr12:108712305 | G | A | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-5-10982C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712305 | |||||||
| chr12:108712399 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-5-11076G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712399 | |||||||
| chr12:108712541 | C | T | 1 | a0001c0001t0005g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-5-11218G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712541 | |||||||
| chr12:108712570 | C | CA | 15 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0310 others(12): Show |
15 | HG01081.hp1 HG01255.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-11248dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712570 | |||||||
| chr12:108712570 | CA | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.-5-11248delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712570 | |||||||
| chr12:108712570 | CAA | C | 60 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0092 others(57): Show |
64 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-5-11249_-5-11248d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712570 | |||||||
| chr12:108712611 | A | G | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG01109.hp1 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-11288T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712611 | |||||||
| chr12:108712642 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(30): Show |
33 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(30): Show |
intron_variant | MODIFIER | c.-5-11319G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712642 | |||||||
| chr12:108712698 | T | C | 1 | a0001c0001t0003g0249 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-5-11375A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712698 | |||||||
| chr12:108712739 | T | C | 1 | a0001c0001t0003g0293 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-5-11416A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712739 | |||||||
| chr12:108712761 | A | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
288 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.-5-11438T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712761 | |||||||
| chr12:108712913 | T | TA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0042 others(38): Show |
41 | HG00099.hp2 HG00423.hp2 HG02083.hp2 others(38): Show |
intron_variant | MODIFIER | c.-5-11591dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712913 | |||||||
| chr12:108712913 | T | TAA | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
174 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-5-11592_-5-11591d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712913 | |||||||
| chr12:108712913 | T | TAAA | 32 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0061 others(29): Show |
32 | HG00140.hp1 HG01167.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.-5-11593_-5-11591d others(5): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712913 | |||||||
| chr12:108712913 | TA | T | 17 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0003g0238 others(14): Show |
17 | HG00140.hp2 HG01069.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5-11591delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108712913 | |||||||
| chr12:108713024 | G | T | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-11701C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108713024 | |||||||
| chr12:108713246 | T | C | 1 | a0001c0001t0004g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5-11923A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108713246 | |||||||
| chr12:108713902 | AT | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG00735.hp1 HG01109.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-12580delA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108713902 | |||||||
| chr12:108714112 | C | A | 17 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-5-12789G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714112 | |||||||
| chr12:108714119 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(242): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-5-12796T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714119 | |||||||
| chr12:108714157 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-5-12834C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714157 | |||||||
| chr12:108714165 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-5-12842G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714165 | |||||||
| chr12:108714186 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-5-12863A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714186 | |||||||
| chr12:108714241 | T | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-12918A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714241 | |||||||
| chr12:108714250 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-5-12927C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714250 | |||||||
| chr12:108714265 | T | C | 2 | a0001c0001t0003g0251 a0001c0001t0003g0252 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-5-12942A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714265 | |||||||
| chr12:108714309 | A | T | 1 | a0001c0001t0003g0320 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-5-12986T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714309 | |||||||
| chr12:108714384 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0170 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5-13061G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714384 | |||||||
| chr12:108714385 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG01358.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-5-13062C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714385 | |||||||
| chr12:108714397 | C | CA | 233 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(230): Show |
238 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.-5-13075dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714397 | |||||||
| chr12:108714530 | G | A | 1 | a0001c0001t0007g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-5-13207C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714530 | |||||||
| chr12:108714556 | T | C | 2 | a0001c0001t0003g0242 a0001c0001t0003g0247 |
2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-5-13233A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714556 | |||||||
| chr12:108714597 | C | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-13274G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714597 | |||||||
| chr12:108714720 | G | A | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-13397C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714720 | |||||||
| chr12:108714812 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-5-13489A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714812 | |||||||
| chr12:108714949 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-5-13626T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108714949 | |||||||
| chr12:108715039 | A | G | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0128 others(7): Show |
10 | HG01884.hp1 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-5-13716T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715039 | |||||||
| chr12:108715048 | T | A | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-5-13725A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715048 | |||||||
| chr12:108715139 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-5-13816G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715139 | |||||||
| chr12:108715144 | A | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-5-13821T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715144 | |||||||
| chr12:108715238 | AAAAAC | A | 5 | a0001c0001t0001g0046 a0001c0001t0003g0250 a0001c0001t0012g0133 others(2): Show |
6 | HG01261.hp1 HG02040.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-13920_-5-13916d others(7): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715238 | |||||||
| chr12:108715318 | CATA | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 |
3 | HG00642.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-5-13998_-5-13996d others(5): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715318 | |||||||
| chr12:108715444 | A | G | 5 | a0001c0001t0005g0184 a0001c0001t0005g0302 a0001c0001t0005g0303 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-14121T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715444 | |||||||
| chr12:108715466 | G | A | 1 | a0001c0001t0007g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-5-14143C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715466 | |||||||
| chr12:108715505 | A | G | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-14182T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715505 | |||||||
| chr12:108715542 | C | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-5-14219G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715542 | |||||||
| chr12:108715642 | C | G | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5-14319G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715642 | |||||||
| chr12:108715650 | C | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0004g0263 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5-14327G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715650 | |||||||
| chr12:108715667 | T | TGCAGAAC others(17): Show |
263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-5-14345_-5-14344i others(26): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715667 | |||||||
| chr12:108715670 | C | A | 51 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(48): Show |
55 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.-5-14347G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715670 | |||||||
| chr12:108715715 | A | G | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5-14392T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715715 | |||||||
| chr12:108715875 | T | C | 1 | a0001c0001t0003g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-5-14552A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715875 | |||||||
| chr12:108715926 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
268 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-5-14603T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108715926 | |||||||
| chr12:108716020 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-5-14697T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716020 | |||||||
| chr12:108716102 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0002g0127 a0005c0007t0001g0047 |
3 | NA18974.hp1 NA18975.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-5-14779A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716102 | |||||||
| chr12:108716127 | C | CA | 34 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0001g0156 others(31): Show |
34 | HG00408.hp2 HG01255.hp1 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-5-14805dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716127 | C | CAA | 8 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0146 others(5): Show |
8 | HG01243.hp2 HG01256.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5-14806_-5-14805d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716127 | CA | C | 105 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(102): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-5-14805delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716127 | CAA | C | 16 | a0001c0001t0001g0073 a0001c0001t0002g0127 a0001c0001t0003g0242 others(13): Show |
16 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5-14806_-5-14805d others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716127 | CAAAA | C | 15 | a0001c0001t0001g0123 a0001c0001t0002g0079 a0001c0001t0002g0081 others(12): Show |
15 | HG00642.hp2 HG00673.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-5-14808_-5-14805d others(6): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716127 | CAAAAA | C | 37 | a0001c0001t0001g0092 a0001c0001t0002g0001 a0001c0001t0002g0078 others(34): Show |
41 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.-5-14809_-5-14805d others(7): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716127 | |||||||
| chr12:108716161 | C | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-5-14838G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716161 | |||||||
| chr12:108716391 | T | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+15038A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716391 | |||||||
| chr12:108716541 | A | G | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+14888T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716541 | |||||||
| chr12:108716757 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6+14672G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716757 | |||||||
| chr12:108716883 | T | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-6+14546A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108716883 | |||||||
| chr12:108717066 | G | A | 2 | a0001c0001t0003g0278 a0001c0001t0007g0277 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-6+14363C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717066 | |||||||
| chr12:108717166 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0267 |
3 | HG01884.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-6+14263T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717166 | |||||||
| chr12:108717191 | C | A | 1 | a0001c0001t0002g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-6+14238G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717191 | |||||||
| chr12:108717195 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-6+14234C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717195 | |||||||
| chr12:108717336 | T | C | 1 | a0001c0001t0003g0314 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-6+14093A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717336 | |||||||
| chr12:108717443 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+13986G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717443 | |||||||
| chr12:108717444 | G | T | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+13985C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717444 | |||||||
| chr12:108717603 | A | G | 1 | a0001c0001t0003g0314 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-6+13826T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717603 | |||||||
| chr12:108717611 | T | C | 1 | a0001c0001t0003g0260 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-6+13818A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717611 | |||||||
| chr12:108717707 | T | G | 2 | a0001c0001t0004g0264 a0001c0001t0004g0265 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-6+13722A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108717707 | |||||||
| chr12:108718092 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+13337C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718092 | |||||||
| chr12:108718369 | GA | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-6+13059delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718369 | |||||||
| chr12:108718371 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0072 |
2 | NA19009.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-6+13058T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718371 | |||||||
| chr12:108718371 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6+13058T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718371 | |||||||
| chr12:108718578 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-6+12851T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718578 | |||||||
| chr12:108718612 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-6+12817A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718612 | |||||||
| chr12:108718669 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-6+12760A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718669 | |||||||
| chr12:108718763 | G | A | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+12666C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718763 | |||||||
| chr12:108718939 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-6+12490A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108718939 | |||||||
| chr12:108719014 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-6+12415A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719014 | |||||||
| chr12:108719308 | C | A | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+12121G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719308 | |||||||
| chr12:108719385 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-6+12044G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719385 | |||||||
| chr12:108719465 | T | C | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-6+11964A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719465 | |||||||
| chr12:108719608 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-6+11821A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719608 | |||||||
| chr12:108719739 | A | G | 1 | a0001c0001t0006g0182 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-6+11690T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719739 | |||||||
| chr12:108719893 | T | G | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-6+11536A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108719893 | |||||||
| chr12:108720305 | T | A | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-6+11124A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108720305 | |||||||
| chr12:108720525 | A | AT | 75 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(72): Show |
76 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-6+10903dupA | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108720525 | |||||||
| chr12:108720624 | G | T | 3 | a0001c0001t0006g0130 a0001c0001t0006g0148 a0001c0001t0006g0162 |
3 | HG02523.hp2 HG03239.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-6+10805C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108720624 | |||||||
| chr12:108720668 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(48): Show |
51 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.-6+10761G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108720668 | |||||||
| chr12:108721251 | C | T | 2 | a0001c0001t0003g0253 a0001c0001t0003g0254 |
2 | HG00140.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-6+10178G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721251 | |||||||
| chr12:108721302 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-6+10127G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721302 | |||||||
| chr12:108721447 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-6+9982G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721447 | |||||||
| chr12:108721458 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-6+9971T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721458 | |||||||
| chr12:108721612 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-6+9817A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721612 | |||||||
| chr12:108721770 | ACAGGACG others(6): Show |
A | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+9646_-6+9658del others(13): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721770 | |||||||
| chr12:108721801 | A | T | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+9628T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721801 | |||||||
| chr12:108721912 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
257 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.-6+9517A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721912 | |||||||
| chr12:108721979 | G | A | 58 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(55): Show |
62 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-6+9450C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721979 | |||||||
| chr12:108721989 | AC | A | 53 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(50): Show |
57 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-6+9439delG | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108721989 | |||||||
| chr12:108722068 | A | C | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-6+9361T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722068 | |||||||
| chr12:108722083 | A | G | 1 | a0001c0001t0003g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-6+9346T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722083 | |||||||
| chr12:108722113 | T | C | 1 | a0001c0001t0012g0133 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-6+9316A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722113 | |||||||
| chr12:108722209 | A | C | 2 | a0001c0001t0003g0251 a0001c0001t0003g0252 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-6+9220T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722209 | |||||||
| chr12:108722506 | C | T | 3 | a0001c0001t0004g0263 a0001c0001t0004g0264 a0001c0001t0004g0265 |
3 | HG02055.hp2 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-6+8923G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722506 | |||||||
| chr12:108722598 | G | A | 4 | a0001c0001t0004g0262 a0001c0001t0004g0294 a0001c0001t0004g0295 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+8831C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722598 | |||||||
| chr12:108722946 | C | T | 12 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6+8483G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108722946 | |||||||
| chr12:108723104 | A | G | 2 | a0001c0001t0001g0261 a0004c0004t0014g0134 |
2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-6+8325T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108723104 | |||||||
| chr12:108723218 | C | A | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6+8211G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108723218 | |||||||
| chr12:108723300 | C | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+8129G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108723300 | |||||||
| chr12:108723475 | T | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+7954A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108723475 | |||||||
| chr12:108723602 | C | A | 58 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0001g0261 others(55): Show |
62 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-6+7827G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108723602 | |||||||
| chr12:108724104 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-6+7325G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724104 | |||||||
| chr12:108724197 | TAACTGAA others(3): Show |
T | 1 | a0001c0001t0002g0084 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-6+7222_-6+7231del others(10): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724197 | |||||||
| chr12:108724213 | C | T | 57 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(54): Show |
61 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-6+7216G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724213 | |||||||
| chr12:108724725 | T | G | 1 | a0001c0001t0002g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6+6704A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724725 | |||||||
| chr12:108724938 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-6+6491G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724938 | |||||||
| chr12:108724999 | C | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+6430G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108724999 | |||||||
| chr12:108725106 | A | G | 19 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(16): Show |
19 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-6+6323T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725106 | |||||||
| chr12:108725146 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-6+6283T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725146 | |||||||
| chr12:108725161 | T | C | 9 | a0001c0001t0003g0283 a0001c0001t0003g0286 a0001c0001t0003g0289 others(6): Show |
9 | HG01433.hp1 HG02109.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-6+6268A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725161 | |||||||
| chr12:108725272 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+6157T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725272 | |||||||
| chr12:108725356 | A | T | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+6073T>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725356 | |||||||
| chr12:108725520 | C | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-6+5909G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725520 | |||||||
| chr12:108725562 | A | G | 2 | a0001c0001t0001g0011 a0003c0008t0001g0010 |
2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-6+5867T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725562 | |||||||
| chr12:108725579 | T | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-6+5850A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725579 | |||||||
| chr12:108725627 | G | A | 3 | a0001c0001t0003g0291 a0001c0001t0003g0293 a0001c0001t0007g0292 |
3 | HG01884.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+5802C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725627 | |||||||
| chr12:108725640 | G | A | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-6+5789C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725640 | |||||||
| chr12:108725643 | A | G | 2 | a0001c0001t0001g0181 a0004c0004t0014g0134 |
2 | HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-6+5786T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725643 | |||||||
| chr12:108725662 | T | C | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-6+5767A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725662 | |||||||
| chr12:108725688 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-6+5741A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725688 | |||||||
| chr12:108725765 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG00438.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-6+5664G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725765 | |||||||
| chr12:108725800 | A | AATTT | 3 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0006g0148 |
3 | HG01099.hp2 HG02109.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-6+5625_-6+5628dup others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725800 | |||||||
| chr12:108725825 | T | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.-6+5604A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725825 | |||||||
| chr12:108725874 | C | A | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6+5555G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725874 | |||||||
| chr12:108725997 | C | A | 1 | a0001c0001t0001g0009 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-6+5432G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108725997 | |||||||
| chr12:108726068 | C | T | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+5361G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726068 | |||||||
| chr12:108726171 | A | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG01167.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6+5258T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726171 | |||||||
| chr12:108726227 | C | G | 1 | a0001c0001t0007g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-6+5202G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726227 | |||||||
| chr12:108726241 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+5188A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726241 | |||||||
| chr12:108726250 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-6+5179A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726250 | |||||||
| chr12:108726358 | G | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+5071C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726358 | |||||||
| chr12:108726446 | A | G | 1 | a0001c0001t0002g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-6+4983T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726446 | |||||||
| chr12:108726563 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00423.hp2 NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-6+4866T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726563 | |||||||
| chr12:108726569 | G | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
53 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-6+4860C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726569 | |||||||
| chr12:108726654 | T | TA | 6 | a0001c0001t0001g0261 a0001c0001t0004g0262 a0001c0001t0004g0294 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+4774dupT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726654 | |||||||
| chr12:108726654 | TA | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0139 others(5): Show |
8 | HG01192.hp1 HG03491.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+4774delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726654 | |||||||
| chr12:108726667 | A | G | 12 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6+4762T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726667 | |||||||
| chr12:108726807 | G | A | 1 | a0001c0001t0003g0297 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-6+4622C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726807 | |||||||
| chr12:108726877 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-6+4552C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108726877 | |||||||
| chr12:108727033 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-6+4396C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727033 | |||||||
| chr12:108727262 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-6+4167G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727262 | |||||||
| chr12:108727342 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA19056.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-6+4087C>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727342 | |||||||
| chr12:108727371 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-6+4058C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727371 | |||||||
| chr12:108727373 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-6+4056A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727373 | |||||||
| chr12:108727495 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+3934G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727495 | |||||||
| chr12:108727559 | T | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+3870A>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727559 | |||||||
| chr12:108727621 | T | C | 1 | a0001c0002t0003g0298 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-6+3808A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727621 | |||||||
| chr12:108727648 | C | T | 2 | a0001c0001t0021g0321 a0004c0004t0014g0134 |
2 | HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+3781G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727648 | |||||||
| chr12:108727670 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-6+3759A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727670 | |||||||
| chr12:108727872 | A | G | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+3557T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727872 | |||||||
| chr12:108727919 | G | A | 76 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(73): Show |
77 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-6+3510C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727919 | |||||||
| chr12:108727983 | A | G | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-6+3446T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108727983 | |||||||
| chr12:108728064 | G | C | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+3365C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728064 | |||||||
| chr12:108728113 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6+3316T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728113 | |||||||
| chr12:108728247 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-6+3182T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728247 | |||||||
| chr12:108728341 | TA | T | 56 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(53): Show |
60 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-6+3087delT | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728341 | |||||||
| chr12:108728373 | A | G | 2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-6+3056T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728373 | |||||||
| chr12:108728492 | G | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-6+2937C>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728492 | |||||||
| chr12:108728581 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-6+2848G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728581 | |||||||
| chr12:108728679 | A | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
251 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-6+2750T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728679 | |||||||
| chr12:108728739 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0021g0321 a0004c0004t0014g0134 |
3 | HG02280.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-6+2690T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728739 | |||||||
| chr12:108728750 | T | C | 3 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 |
3 | NA18957.hp2 NA18983.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-6+2679A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728750 | |||||||
| chr12:108728871 | G | A | 1 | a0001c0001t0002g0127 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-6+2558C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728871 | |||||||
| chr12:108728878 | A | C | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-6+2551T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108728878 | |||||||
| chr12:108729105 | T | C | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+2324A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729105 | |||||||
| chr12:108729240 | C | T | 1 | a0004c0004t0014g0134 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-6+2189G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729240 | |||||||
| chr12:108729288 | A | G | 24 | a0001c0001t0003g0238 a0001c0001t0003g0239 a0001c0001t0003g0241 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.-6+2141T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729288 | |||||||
| chr12:108729379 | T | C | 1 | a0001c0001t0004g0299 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-6+2050A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729379 | |||||||
| chr12:108729388 | GGTAT | G | 52 | a0001c0001t0001g0092 a0001c0001t0001g0123 a0001c0001t0002g0001 others(49): Show |
56 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-6+2037_-6+2040del others(4): Show |
CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729388 | |||||||
| chr12:108729390 | T | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0009g0267 |
3 | HG01884.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-6+2039A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729390 | |||||||
| chr12:108729401 | T | A | 1 | a0001c0001t0020g0300 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-6+2028A>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729401 | |||||||
| chr12:108729678 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-6+1751C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729678 | |||||||
| chr12:108729996 | C | T | 2 | a0001c0001t0012g0133 a0001c0001t0013g0132 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-6+1433G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108729996 | |||||||
| chr12:108730007 | C | A | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0010g0235 |
3 | HG00099.hp2 HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-6+1422G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730007 | |||||||
| chr12:108730121 | G | A | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+1308C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730121 | |||||||
| chr12:108730122 | A | G | 1 | a0001c0001t0015g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-6+1307T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730122 | |||||||
| chr12:108730353 | C | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
251 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-6+1076G>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730353 | |||||||
| chr12:108730485 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-6+944C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730485 | |||||||
| chr12:108730522 | T | C | 1 | a0001c0001t0003g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-6+907A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730522 | |||||||
| chr12:108730796 | C | T | 1 | a0001c0001t0006g0130 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-6+633G>A | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730796 | |||||||
| chr12:108730845 | C | A | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-6+584G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730845 | |||||||
| chr12:108730938 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
135 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-6+491T>C | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108730938 | |||||||
| chr12:108731165 | G | A | 4 | a0001c0001t0005g0302 a0001c0001t0005g0303 a0001c0001t0005g0304 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+264C>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108731165 | |||||||
| chr12:108731171 | T | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | HG02280.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-6+258A>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108731171 | |||||||
| chr12:108731235 | AG | A | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG01081.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-6+193delC | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108731235 | |||||||
| chr12:108731237 | C | A | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG01081.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-6+192G>T | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108731237 | |||||||
| chr12:108731419 | A | C | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-6+10T>G | CORO1C | ENSG00000110880.11 | transcript | ENST00000261401.8 | protein_coding | 1/10 | chr12 | 108731419 |