Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9541 |
| ensemblid | ENSG00000138433.16 |
| hgncid | 24217 |
| symbol | CIR1 |
| name | corepressor interacting with RBPJ, CIR1 |
| refseq_nuc | NM_004882.4 |
| refseq_prot | NP_004873.3 |
| ensembl_nuc | ENST00000342016.8 |
| ensembl_prot | ENSP00000339723.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 174348022 |
| end | 174395712 |
| strand | - |
| ver | v1.2 |
| region | chr2:174348022-174395712 |
| region5000 | chr2:174343022-174400712 |
| regionname0 | CIR1_chr2_174348022_174395712 |
| regionname5000 | CIR1_chr2_174343022_174400712 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 450 | 325 | 70 | 62 | 131 | 14 | 46 | 103 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0002 | 0/0 | 450 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0003 | 0/0 | 450 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0004 | 0/0 | 450 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0005 | 0/0 | 450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0006 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| a0007 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | MGKSF others(445): Show |
chr2 | 174343022 | 174400712 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1350 | 325 | 70 | 62 | 131 | 14 | 46 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0002c0002 | 0/0 | 1350 | 16 | 15 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0003c0003 | 0/0 | 1350 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0004c0004 | 0/0 | 1350 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0005c0007 | 0/0 | 1350 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0006c0005 | 0/0 | 1350 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 | ||
| a0007c0006 | 0/0 | 1350 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | ATGGG others(1345): Show |
chr2 | 174343022 | 174400712 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1918 | 174 | 15 | 41 | 79 | 12 | 27 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0002 | 1/1 | 1918 | 132 | 50 | 15 | 48 | 2 | 15 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0003 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0004 | 0/0 | 1918 | 7 | 0 | 6 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0005 | 0/0 | 1918 | 5 | 5 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0006 | 0/0 | 1918 | 2 | 0 | 0 | 0 | 0 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0007 | 0/0 | 1918 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0008 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0001c0001t0009 | 0/0 | 1918 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0002c0002t0003 | 0/0 | 1918 | 16 | 15 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0003c0003t0001 | 0/0 | 1918 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0004c0004t0001 | 0/0 | 1918 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0005c0007t0001 | 0/0 | 1918 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0006c0005t0002 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| a0007c0006t0001 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | GCTGC others(1913): Show |
chr2 | 174343022 | 174400712 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0001c0001t0009g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0002c0002t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0003c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0004c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0005c0007t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0006c0005t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| a0007c0006t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00735 | hp1 | a0002 | c0002 | t0003 | g0012 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01952 | hp1 | a0005 | c0007 | t0001 | g0126 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0305 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0043 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0281 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0222 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0224 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0013 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0058 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0230 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0056 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02965 | hp1 | a0002 | c0002 | t0003 | g0304 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0013 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0014 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0054 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | GWD | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0032 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18522 | hp1 | a0006 | c0005 | t0002 | g0204 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0008 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19004 | hp1 | a0007 | c0006 | t0001 | g0299 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19056 | hp1 | a0004 | c0004 | t0001 | g0287 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19058 | hp2 | a0004 | c0004 | t0001 | g0289 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ASW | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20129 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | ASW | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | GIH | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | USA | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | LWK | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0241 | REF | REF | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0176 | REF | REF | CIR1_chr2_174343022_174400712 | CIR1 | chr2 | 174343022 | 174400712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174348679 | G | A | 1 | a0007 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.1171C>T | p.Arg391Trp | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 1261/1918 | 1171/1353 | 391/450 | chr2 | 174348679 | |||
| chr2:174348917 | G | C | 1 | a0002 | 16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
missense_variant | MODERATE | c.933C>G | p.Asp311Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 1023/1918 | 933/1353 | 311/450 | chr2 | 174348917 | |||
| chr2:174349123 | T | C | 1 | a0003 | 2 | HG03209.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.727A>G | p.Lys243Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 817/1918 | 727/1353 | 243/450 | chr2 | 174349123 | |||
| chr2:174349141 | T | C | 1 | a0004 | 2 | NA19056.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.709A>G | p.Lys237Glu | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 799/1918 | 709/1353 | 237/450 | chr2 | 174349141 | |||
| chr2:174378931 | T | C | 1 | a0005 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.476A>G | p.Asp159Gly | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/10 | 566/1918 | 476/1353 | 159/450 | chr2 | 174378931 | |||
| chr2:174378941 | C | T | 1 | a0006 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.466G>A | p.Val156Ile | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/10 | 556/1918 | 466/1353 | 156/450 | chr2 | 174378941 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174348127 | T | C | 1 | a0001c0001t0006 | 2 | HG02735.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*370A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 370 | chr2 | 174348127 | ||||||
| chr2:174348135 | A | T | 2 | a0001c0001t0003 a0002c0002t0003 |
17 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*362T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 362 | chr2 | 174348135 | ||||||
| chr2:174348244 | A | C | 1 | a0001c0001t0005 | 5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*253T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 253 | chr2 | 174348244 | ||||||
| chr2:174348313 | T | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(6): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*184A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 184 | chr2 | 174348313 | ||||||
| chr2:174348471 | T | C | 1 | a0001c0001t0007 | 2 | NA18948.hp1 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 26 | chr2 | 174348471 | ||||||
| chr2:174348475 | G | A | 1 | a0001c0001t0009 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 10/10 | 22 | chr2 | 174348475 | ||||||
| chr2:174395627 | G | T | 1 | a0001c0001t0004 | 7 | HG00733.hp2 HG01261.hp1 HG01361.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/10 | 5 | chr2 | 174395627 | ||||||
| chr2:174395646 | C | T | 1 | a0001c0001t0008 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/10 | 24 | chr2 | 174395646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174349275 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.678-103A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349275 | |||||||
| chr2:174349538 | T | A | 190 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(187): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.678-366A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349538 | |||||||
| chr2:174349564 | T | TA | 7 | a0001c0001t0002g0179 a0001c0001t0002g0194 a0001c0001t0002g0215 others(4): Show |
7 | HG00673.hp2 HG02027.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.678-393dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | |||||||
| chr2:174349564 | TA | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0166 a0001c0001t0001g0211 others(60): Show |
72 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.678-393delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | |||||||
| chr2:174349564 | TAA | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.678-394_678-393del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349564 | |||||||
| chr2:174349741 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.678-569A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349741 | |||||||
| chr2:174349859 | A | G | 5 | a0001c0001t0005g0053 a0001c0001t0005g0098 a0001c0001t0005g0115 others(2): Show |
5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.678-687T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174349859 | |||||||
| chr2:174350050 | T | G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677+610A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350050 | |||||||
| chr2:174350168 | ACT | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(91): Show |
106 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.677+490_677+491del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350168 | |||||||
| chr2:174350202 | A | G | 10 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0041 others(7): Show |
12 | HG00408.hp1 HG00642.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.677+458T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350202 | |||||||
| chr2:174350559 | G | A | 27 | a0001c0001t0001g0211 a0001c0001t0002g0002 a0001c0001t0002g0021 others(24): Show |
32 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.677+101C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 9/9 | chr2 | 174350559 | |||||||
| chr2:174351006 | C | G | 1 | a0001c0001t0002g0022 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.592-261G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351006 | |||||||
| chr2:174351058 | T | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.592-313A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351058 | |||||||
| chr2:174351098 | A | T | 1 | a0001c0001t0002g0187 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.592-353T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351098 | |||||||
| chr2:174351272 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.591+347T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351272 | |||||||
| chr2:174351303 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.591+316T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351303 | |||||||
| chr2:174351463 | T | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0205 a0001c0001t0001g0206 others(10): Show |
14 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.591+156A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351463 | |||||||
| chr2:174351498 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+121A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 8/9 | chr2 | 174351498 | |||||||
| chr2:174351801 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-76C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174351801 | |||||||
| chr2:174351886 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.485-161T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174351886 | |||||||
| chr2:174352205 | T | TCA | 58 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(55): Show |
76 | HG00558.hp2 HG00673.hp2 HG01884.hp1 others(73): Show |
intron_variant | MODIFIER | c.485-482_485-481dup others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352205 | |||||||
| chr2:174352205 | TCA | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-482_485-481del others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352205 | |||||||
| chr2:174352228 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-503A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352228 | |||||||
| chr2:174352447 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.485-722T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352447 | |||||||
| chr2:174352470 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485-745A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352470 | |||||||
| chr2:174352508 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-783T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352508 | |||||||
| chr2:174352559 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-834T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352559 | |||||||
| chr2:174352616 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-891C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352616 | |||||||
| chr2:174352617 | C | G | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-892G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352617 | |||||||
| chr2:174352944 | C | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-1219G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352944 | |||||||
| chr2:174352963 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-1238G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174352963 | |||||||
| chr2:174353113 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485-1388G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353113 | |||||||
| chr2:174353114 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0164 |
2 | HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.485-1389C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353114 | |||||||
| chr2:174353188 | G | T | 1 | a0003c0003t0001g0014 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.485-1463C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353188 | |||||||
| chr2:174353225 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.485-1500G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353225 | |||||||
| chr2:174353312 | T | C | 1 | a0002c0002t0003g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485-1587A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353312 | |||||||
| chr2:174353429 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.485-1704G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353429 | |||||||
| chr2:174353470 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.485-1745A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353470 | |||||||
| chr2:174353555 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0140 |
3 | HG03704.hp2 HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.485-1830G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353555 | |||||||
| chr2:174353603 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-1878C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353603 | |||||||
| chr2:174353605 | T | C | 14 | a0001c0001t0002g0047 a0001c0001t0002g0105 a0001c0001t0002g0107 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-1880A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353605 | |||||||
| chr2:174353640 | G | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-1915C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353640 | |||||||
| chr2:174353640 | G | C | 14 | a0001c0001t0002g0047 a0001c0001t0002g0105 a0001c0001t0002g0107 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-1915C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353640 | |||||||
| chr2:174353706 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.485-1981A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353706 | |||||||
| chr2:174353745 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-2020G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353745 | |||||||
| chr2:174353932 | C | G | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 |
3 | HG02615.hp2 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485-2207G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353932 | |||||||
| chr2:174353979 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.485-2254G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174353979 | |||||||
| chr2:174354205 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2480A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354205 | |||||||
| chr2:174354266 | C | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2541G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354266 | |||||||
| chr2:174354310 | A | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-2585T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354310 | |||||||
| chr2:174354382 | TA | T | 3 | a0001c0001t0002g0097 a0001c0001t0002g0103 a0001c0001t0002g0104 |
3 | HG02559.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.485-2658delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354382 | |||||||
| chr2:174354413 | A | AT | 11 | a0002c0002t0003g0008 a0002c0002t0003g0012 a0002c0002t0003g0013 others(8): Show |
15 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.485-2689dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354413 | |||||||
| chr2:174354414 | TATAA | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0249 a0002c0002t0003g0054 |
3 | HG01123.hp1 HG03225.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.485-2693_485-2690d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354414 | |||||||
| chr2:174354431 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-2706C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354431 | |||||||
| chr2:174354435 | TATATA | T | 7 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0081 others(4): Show |
7 | HG01074.hp2 HG02717.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-2715_485-2711d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354435 | |||||||
| chr2:174354441 | ATATAT | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(177): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.485-2721_485-2717d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354441 | |||||||
| chr2:174354442 | TATATTAT others(3): Show |
T | 1 | a0001c0001t0001g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.485-2727_485-2718d others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354442 | |||||||
| chr2:174354446 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.485-2721A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354446 | |||||||
| chr2:174354447 | T | A | 11 | a0001c0001t0002g0045 a0001c0001t0003g0201 a0002c0002t0003g0008 others(8): Show |
15 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.485-2722A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354447 | |||||||
| chr2:174354447 | TATATA | T | 7 | a0001c0001t0002g0047 a0001c0001t0002g0116 a0001c0001t0002g0202 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-2727_485-2723d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354447 | |||||||
| chr2:174354454 | TATA | T | 7 | a0001c0001t0002g0018 a0001c0001t0002g0131 a0001c0001t0002g0175 others(4): Show |
10 | HG02055.hp1 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-2732_485-2730d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354454 | |||||||
| chr2:174354491 | TATAAATT others(14): Show |
T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0017 others(77): Show |
88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.485-2787_485-2767d others(23): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354491 | |||||||
| chr2:174354495 | A | AATTATAT others(42): Show |
1 | a0001c0001t0001g0211 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485-2819_485-2771d others(51): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354495 | |||||||
| chr2:174354495 | A | T | 1 | a0001c0001t0001g0158 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.485-2770T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354495 | |||||||
| chr2:174354505 | TATATATC | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(93): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.485-2787_485-2781d others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354505 | |||||||
| chr2:174354517 | A | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-2792T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354517 | |||||||
| chr2:174354538 | A | AATATATA others(30): Show |
30 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0019 others(27): Show |
39 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.485-2850_485-2814d others(39): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354538 | |||||||
| chr2:174354538 | A | AATATATA others(27): Show |
1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-2814_485-2813i others(36): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354538 | |||||||
| chr2:174354541 | ATATAT | A | 9 | a0001c0001t0003g0201 a0002c0002t0003g0012 a0002c0002t0003g0013 others(6): Show |
11 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-2821_485-2817d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354541 | |||||||
| chr2:174354561 | TTTATATA others(40): Show |
T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(172): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.485-2883_485-2837d others(49): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354561 | |||||||
| chr2:174354562 | T | TTATATAT others(56): Show |
1 | a0001c0001t0002g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-2838_485-2837i others(65): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | |||||||
| chr2:174354562 | T | TTATATAT others(58): Show |
2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-2838_485-2837i others(67): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | |||||||
| chr2:174354562 | T | TTATATAT others(28): Show |
6 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0235 others(3): Show |
6 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-2872_485-2838d others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354562 | |||||||
| chr2:174354575 | T | G | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-2850A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | |||||||
| chr2:174354575 | T | TATATATA others(30): Show |
4 | a0001c0001t0002g0009 a0001c0001t0002g0037 a0001c0001t0002g0184 others(1): Show |
5 | NA18942.hp2 NA18954.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2851_485-2850i others(39): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | |||||||
| chr2:174354575 | T | TATATATA others(88): Show |
1 | a0001c0001t0002g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.485-2851_485-2850i others(97): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | |||||||
| chr2:174354575 | T | TATATATT others(28): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.485-2851_485-2850i others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354575 | |||||||
| chr2:174354578 | ATAT | A | 5 | a0001c0001t0005g0053 a0001c0001t0005g0098 a0001c0001t0005g0115 others(2): Show |
5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2856_485-2854d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354578 | |||||||
| chr2:174354583 | A | ATATATCA others(26): Show |
2 | a0001c0001t0002g0045 a0001c0001t0002g0117 |
2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.485-2859_485-2858i others(35): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354583 | |||||||
| chr2:174354583 | ATATATAT others(28): Show |
A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2893_485-2859d others(37): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354583 | |||||||
| chr2:174354591 | C | A | 5 | a0001c0001t0002g0102 a0001c0001t0002g0106 a0001c0001t0003g0201 others(2): Show |
5 | HG02258.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-2866G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354591 | |||||||
| chr2:174354615 | A | ATTTTATA others(24): Show |
7 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0043 others(4): Show |
9 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-2921_485-2891d others(33): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354615 | |||||||
| chr2:174354626 | T | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-2901A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354626 | |||||||
| chr2:174354626 | T | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0104 a0001c0001t0002g0108 |
3 | HG02055.hp2 HG02257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.485-2901A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354626 | |||||||
| chr2:174354689 | T | A | 1 | a0001c0001t0002g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.485-2964A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354689 | |||||||
| chr2:174354764 | A | G | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-3039T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354764 | |||||||
| chr2:174354768 | A | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0063 |
2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.485-3043T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354768 | |||||||
| chr2:174354769 | TA | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0120 a0001c0001t0001g0145 others(2): Show |
5 | HG00438.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-3045delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354769 | |||||||
| chr2:174354770 | A | T | 53 | a0001c0001t0001g0211 a0001c0001t0002g0001 a0001c0001t0002g0002 others(50): Show |
63 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.485-3045T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354770 | |||||||
| chr2:174354770 | AT | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(168): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.485-3046delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354770 | |||||||
| chr2:174354771 | T | TA | 5 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(2): Show |
5 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-3047_485-3046i others(3): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354771 | |||||||
| chr2:174354772 | T | A | 14 | a0001c0001t0001g0136 a0001c0001t0002g0004 a0001c0001t0002g0005 others(11): Show |
20 | HG00673.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-3047A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354772 | |||||||
| chr2:174354773 | T | A | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0290 others(1): Show |
4 | HG01099.hp2 HG01169.hp1 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-3048A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354773 | |||||||
| chr2:174354847 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.485-3122G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354847 | |||||||
| chr2:174354882 | G | A | 1 | a0001c0001t0005g0098 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.485-3157C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354882 | |||||||
| chr2:174354928 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-3203G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174354928 | |||||||
| chr2:174355073 | C | A | 1 | a0001c0001t0001g0015 | 2 | NA19005.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.485-3348G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355073 | |||||||
| chr2:174355218 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0003g0201 |
2 | HG01928.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-3493C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355218 | |||||||
| chr2:174355228 | T | C | 13 | a0001c0001t0002g0022 a0002c0002t0003g0008 a0002c0002t0003g0012 others(10): Show |
18 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-3503A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355228 | |||||||
| chr2:174355247 | C | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-3522G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355247 | |||||||
| chr2:174355361 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-3636A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355361 | |||||||
| chr2:174355425 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.485-3700T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355425 | |||||||
| chr2:174355563 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.485-3838A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355563 | |||||||
| chr2:174355688 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-3963C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355688 | |||||||
| chr2:174355792 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-4067A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355792 | |||||||
| chr2:174355853 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-4128A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355853 | |||||||
| chr2:174355866 | G | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0303 |
2 | NA18956.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.485-4141C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355866 | |||||||
| chr2:174355877 | A | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0074 others(2): Show |
5 | HG00609.hp2 HG02083.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-4152T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355877 | |||||||
| chr2:174355915 | ACTTGTGT others(26): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.485-4223_485-4191d others(35): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355915 | |||||||
| chr2:174355956 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.485-4231G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174355956 | |||||||
| chr2:174356008 | G | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG02015.hp1 HG02040.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-4283C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356008 | |||||||
| chr2:174356076 | A | G | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-4351T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356076 | |||||||
| chr2:174356185 | G | T | 1 | a0001c0001t0002g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485-4460C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356185 | |||||||
| chr2:174356191 | C | T | 1 | a0001c0001t0005g0115 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.485-4466G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356191 | |||||||
| chr2:174356215 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0076 |
2 | HG00438.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.485-4490G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356215 | |||||||
| chr2:174356503 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-4778C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356503 | |||||||
| chr2:174356522 | A | AGGAAGGA others(6): Show |
1 | a0001c0001t0001g0297 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.485-4798_485-4797i others(15): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356522 | |||||||
| chr2:174356522 | A | AGGAAGGA others(10): Show |
1 | a0001c0001t0001g0006 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.485-4798_485-4797i others(19): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356522 | |||||||
| chr2:174356526 | A | AG | 4 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0121 others(1): Show |
4 | HG02165.hp1 HG03017.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-4802dupC | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAG | 78 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0051 others(75): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAGGA others(2): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0001t0001g0073 others(7): Show |
10 | HG00408.hp2 HG00597.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(11): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAGGA others(6): Show |
60 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(57): Show |
66 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(15): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAGGA others(10): Show |
21 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0119 others(18): Show |
23 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.485-4802_485-4801i others(19): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAGGA others(14): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0141 |
2 | HG00280.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.485-4802_485-4801i others(23): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | AGGAAGGA others(22): Show |
1 | a0001c0001t0001g0137 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.485-4802_485-4801i others(31): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356526 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0297 |
2 | HG00609.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.485-4801T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356526 | |||||||
| chr2:174356531 | A | AAAGGAAG others(17): Show |
1 | a0001c0001t0002g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.485-4807_485-4806i others(26): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | |||||||
| chr2:174356531 | A | AAAGGAAG others(29): Show |
2 | a0001c0001t0002g0101 a0001c0001t0002g0102 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-4807_485-4806i others(38): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | |||||||
| chr2:174356531 | A | AAAGGAAG others(17): Show |
1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-4807_485-4806i others(26): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | |||||||
| chr2:174356531 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(172): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.485-4806T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356531 | |||||||
| chr2:174356533 | A | AGGAAGGA others(13): Show |
12 | a0002c0002t0003g0008 a0002c0002t0003g0012 a0002c0002t0003g0013 others(9): Show |
16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-4809_485-4808i others(22): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356533 | |||||||
| chr2:174356601 | GGGAA | G | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-4880_485-4877d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356601 | |||||||
| chr2:174356603 | G | GAGGA | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(171): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.485-4879_485-4878i others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356603 | |||||||
| chr2:174356605 | A | G | 293 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(290): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.485-4880T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356605 | |||||||
| chr2:174356620 | AGAAGGG | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0213 |
3 | HG00639.hp2 HG01109.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.485-4901_485-4896d others(8): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356620 | |||||||
| chr2:174356675 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485-4950G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356675 | |||||||
| chr2:174356677 | C | G | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-4952G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356677 | |||||||
| chr2:174356680 | A | C | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-4955T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356680 | |||||||
| chr2:174356808 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.485-5083C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356808 | |||||||
| chr2:174356831 | T | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG00639.hp1 HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.485-5106A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356831 | |||||||
| chr2:174356926 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.485-5201A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356926 | |||||||
| chr2:174356981 | C | G | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-5256G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174356981 | |||||||
| chr2:174357106 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-5381A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357106 | |||||||
| chr2:174357288 | T | G | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-5563A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357288 | |||||||
| chr2:174357322 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-5597A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357322 | |||||||
| chr2:174357348 | A | G | 14 | a0001c0001t0002g0047 a0001c0001t0002g0105 a0001c0001t0002g0107 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-5623T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357348 | |||||||
| chr2:174357486 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-5761A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357486 | |||||||
| chr2:174357513 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | NA18947.hp1 NA18968.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.485-5788A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357513 | |||||||
| chr2:174357558 | C | T | 5 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0049 others(2): Show |
6 | HG01891.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-5833G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357558 | |||||||
| chr2:174357690 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-5965A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357690 | |||||||
| chr2:174357820 | A | G | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-6095T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357820 | |||||||
| chr2:174357873 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.485-6148A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357873 | |||||||
| chr2:174357974 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-6249A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174357974 | |||||||
| chr2:174358383 | C | T | 2 | a0001c0001t0002g0233 a0001c0001t0002g0235 |
2 | HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.485-6658G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358383 | |||||||
| chr2:174358399 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-6674G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358399 | |||||||
| chr2:174358401 | G | C | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.485-6676C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358401 | |||||||
| chr2:174358524 | C | T | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-6799G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358524 | |||||||
| chr2:174358568 | T | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-6843A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358568 | |||||||
| chr2:174358675 | G | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0286 |
2 | NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.485-6950C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358675 | |||||||
| chr2:174358869 | C | T | 4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(1): Show |
4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-7144G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358869 | |||||||
| chr2:174358917 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.485-7192C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358917 | |||||||
| chr2:174358927 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.485-7202C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358927 | |||||||
| chr2:174358963 | G | A | 12 | a0002c0002t0003g0008 a0002c0002t0003g0012 a0002c0002t0003g0013 others(9): Show |
16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-7238C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358963 | |||||||
| chr2:174358963 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.485-7238C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358963 | |||||||
| chr2:174358973 | C | T | 8 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0235 others(5): Show |
8 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.485-7248G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174358973 | |||||||
| chr2:174359030 | A | T | 4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(1): Show |
4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-7305T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359030 | |||||||
| chr2:174359111 | T | C | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-7386A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359111 | |||||||
| chr2:174359130 | T | TAAG | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-7408_485-7406d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359130 | |||||||
| chr2:174359207 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-7482A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359207 | |||||||
| chr2:174359278 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.485-7553A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359278 | |||||||
| chr2:174359334 | TA | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(194): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.485-7610delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | |||||||
| chr2:174359334 | TAA | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0144 others(8): Show |
11 | HG00323.hp2 HG00597.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.485-7611_485-7610d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | |||||||
| chr2:174359334 | TAAA | T | 14 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(11): Show |
18 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-7612_485-7610d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359334 | |||||||
| chr2:174359491 | T | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0259 a0001c0001t0001g0261 others(1): Show |
4 | HG01256.hp1 HG01981.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-7766A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359491 | |||||||
| chr2:174359535 | G | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0286 |
2 | NA18956.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.485-7810C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359535 | |||||||
| chr2:174359536 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.485-7811G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359536 | |||||||
| chr2:174359593 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0003g0201 |
2 | HG03195.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-7868G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359593 | |||||||
| chr2:174359595 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.485-7870G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359595 | |||||||
| chr2:174359670 | G | A | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-7945C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359670 | |||||||
| chr2:174359844 | A | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8119T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359844 | |||||||
| chr2:174359845 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8120A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359845 | |||||||
| chr2:174359863 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8138A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359863 | |||||||
| chr2:174359864 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8139C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359864 | |||||||
| chr2:174359871 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.485-8146A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359871 | |||||||
| chr2:174359970 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.485-8245T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174359970 | |||||||
| chr2:174360021 | G | A | 4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(1): Show |
4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.485-8296C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360021 | |||||||
| chr2:174360140 | C | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8415G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360140 | |||||||
| chr2:174360183 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.485-8458T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360183 | |||||||
| chr2:174360201 | A | G | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.485-8476T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360201 | |||||||
| chr2:174360219 | A | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0133 |
3 | NA18977.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.485-8494T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360219 | |||||||
| chr2:174360245 | TTTA | T | 13 | a0001c0001t0003g0201 a0002c0002t0003g0008 a0002c0002t0003g0012 others(10): Show |
17 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.485-8523_485-8521d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360245 | |||||||
| chr2:174360290 | C | T | 6 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0235 others(3): Show |
6 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-8565G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360290 | |||||||
| chr2:174360326 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0116 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.485-8601A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360326 | |||||||
| chr2:174360479 | G | T | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-8754C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360479 | |||||||
| chr2:174360753 | T | A | 1 | a0001c0001t0002g0038 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.485-9028A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360753 | |||||||
| chr2:174360898 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(189): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.485-9173T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360898 | |||||||
| chr2:174360986 | G | T | 12 | a0002c0002t0003g0008 a0002c0002t0003g0012 a0002c0002t0003g0013 others(9): Show |
16 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-9261C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174360986 | |||||||
| chr2:174361071 | AATCAACT others(3): Show |
A | 8 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0049 others(5): Show |
9 | HG01891.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-9356_485-9347d others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361071 | |||||||
| chr2:174361380 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-9655C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361380 | |||||||
| chr2:174361522 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0003g0201 |
3 | HG02965.hp2 HG03139.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.485-9797C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361522 | |||||||
| chr2:174361561 | G | A | 5 | a0001c0001t0005g0053 a0001c0001t0005g0098 a0001c0001t0005g0115 others(2): Show |
5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-9836C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361561 | |||||||
| chr2:174361647 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.485-9922G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361647 | |||||||
| chr2:174361914 | T | G | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.485-10189A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174361914 | |||||||
| chr2:174362086 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.485-10361G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362086 | |||||||
| chr2:174362090 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.485-10365C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362090 | |||||||
| chr2:174362107 | G | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.485-10382C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362107 | |||||||
| chr2:174362108 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0149 a0001c0001t0001g0160 |
3 | HG00280.hp1 HG01981.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.485-10383C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362108 | |||||||
| chr2:174362155 | A | C | 5 | a0001c0001t0003g0201 a0002c0002t0003g0008 a0002c0002t0003g0230 others(2): Show |
7 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-10430T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362155 | |||||||
| chr2:174362366 | A | ATAACT | 90 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(87): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.485-10642_485-1064 others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362366 | |||||||
| chr2:174362556 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.485-10831C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362556 | |||||||
| chr2:174362652 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0073 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.485-10927T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362652 | |||||||
| chr2:174362685 | TCA | T | 43 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0072 others(40): Show |
43 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.485-10962_485-1096 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362685 | |||||||
| chr2:174362685 | TCAA | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(127): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.485-10963_485-1096 others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362685 | |||||||
| chr2:174362686 | C | CA | 66 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(63): Show |
82 | HG00558.hp2 HG00639.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.485-10962dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362686 | |||||||
| chr2:174362686 | C | CAA | 24 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0049 others(21): Show |
25 | HG00673.hp2 HG01891.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.485-10963_485-1096 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362686 | |||||||
| chr2:174362718 | TTACATTT others(1): Show |
T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(171): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.485-11001_485-1099 others(12): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362718 | |||||||
| chr2:174362773 | G | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(90): Show |
105 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.485-11048C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174362773 | |||||||
| chr2:174363029 | G | A | 8 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(5): Show |
10 | HG02258.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.485-11304C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363029 | |||||||
| chr2:174363086 | A | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.485-11361T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363086 | |||||||
| chr2:174363089 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.485-11364A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363089 | |||||||
| chr2:174363205 | C | G | 10 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0011 others(7): Show |
16 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-11480G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363205 | |||||||
| chr2:174363334 | T | C | 20 | a0001c0001t0001g0211 a0001c0001t0002g0002 a0001c0001t0002g0021 others(17): Show |
25 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.485-11609A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363334 | |||||||
| chr2:174363501 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-11776G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363501 | |||||||
| chr2:174363752 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-12027G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363752 | |||||||
| chr2:174363773 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0190 |
3 | HG02965.hp2 HG03139.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.485-12048C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363773 | |||||||
| chr2:174363809 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.485-12084T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363809 | |||||||
| chr2:174363811 | G | T | 5 | a0001c0001t0003g0201 a0002c0002t0003g0008 a0002c0002t0003g0230 others(2): Show |
7 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-12086C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363811 | |||||||
| chr2:174363882 | G | A | 1 | a0006c0005t0002g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485-12157C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363882 | |||||||
| chr2:174363915 | C | T | 1 | a0001c0001t0008g0028 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.485-12190G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363915 | |||||||
| chr2:174363925 | C | A | 14 | a0001c0001t0002g0047 a0001c0001t0002g0105 a0001c0001t0002g0107 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-12200G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363925 | |||||||
| chr2:174363941 | A | G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.485-12216T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174363941 | |||||||
| chr2:174364180 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.485-12455A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364180 | |||||||
| chr2:174364201 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.485-12476C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364201 | |||||||
| chr2:174364269 | T | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-12544A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364269 | |||||||
| chr2:174364360 | G | A | 4 | a0002c0002t0003g0008 a0002c0002t0003g0230 a0002c0002t0003g0304 others(1): Show |
6 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-12635C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364360 | |||||||
| chr2:174364480 | T | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.485-12755A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364480 | |||||||
| chr2:174364656 | C | T | 1 | a0001c0001t0008g0028 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.485-12931G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364656 | |||||||
| chr2:174364876 | T | C | 53 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(50): Show |
70 | HG00558.hp2 HG00673.hp2 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.485-13151A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364876 | |||||||
| chr2:174364883 | TTC | T | 5 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0049 others(2): Show |
6 | HG01891.hp2 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-13160_485-1315 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364883 | |||||||
| chr2:174364904 | C | T | 297 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(294): Show |
338 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.485-13179G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364904 | |||||||
| chr2:174364925 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.485-13200A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364925 | |||||||
| chr2:174364934 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.485-13209C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364934 | |||||||
| chr2:174364990 | T | C | 17 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0174 others(14): Show |
23 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.485-13265A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174364990 | |||||||
| chr2:174365046 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.485-13321G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365046 | |||||||
| chr2:174365289 | C | T | 5 | a0001c0001t0005g0053 a0001c0001t0005g0098 a0001c0001t0005g0115 others(2): Show |
5 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-13564G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365289 | |||||||
| chr2:174365705 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.484+13218C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365705 | |||||||
| chr2:174365712 | C | G | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+13211G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365712 | |||||||
| chr2:174365928 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.484+12995T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174365928 | |||||||
| chr2:174366092 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.484+12831A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366092 | |||||||
| chr2:174366134 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.484+12789C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366134 | |||||||
| chr2:174366552 | C | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(181): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.484+12371G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366552 | |||||||
| chr2:174366718 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.484+12205T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366718 | |||||||
| chr2:174366846 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(208): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.484+12077T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366846 | |||||||
| chr2:174366869 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484+12054G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366869 | |||||||
| chr2:174366887 | C | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(213): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+12036G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366887 | |||||||
| chr2:174366934 | C | T | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+11989G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366934 | |||||||
| chr2:174366957 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.484+11966T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174366957 | |||||||
| chr2:174367011 | C | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(213): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+11912G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367011 | |||||||
| chr2:174367056 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.484+11867T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367056 | |||||||
| chr2:174367228 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.484+11695T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367228 | |||||||
| chr2:174367260 | G | A | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+11663C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367260 | |||||||
| chr2:174367296 | G | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.484+11627C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367296 | |||||||
| chr2:174367302 | G | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.484+11621C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367302 | |||||||
| chr2:174367329 | C | G | 1 | a0006c0005t0002g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.484+11594G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367329 | |||||||
| chr2:174367355 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.484+11568C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367355 | |||||||
| chr2:174367488 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(83): Show |
95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.484+11435C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367488 | |||||||
| chr2:174367493 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.484+11430A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367493 | |||||||
| chr2:174367495 | G | A | 1 | a0001c0001t0007g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.484+11428C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367495 | |||||||
| chr2:174367715 | C | T | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+11208G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367715 | |||||||
| chr2:174367745 | T | TA | 96 | a0001c0001t0001g0080 a0001c0001t0001g0162 a0001c0001t0001g0207 others(93): Show |
120 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.484+11177dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | |||||||
| chr2:174367745 | T | TAA | 13 | a0001c0001t0002g0022 a0001c0001t0002g0045 a0001c0001t0002g0055 others(10): Show |
14 | HG01884.hp1 HG02080.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.484+11176_484+1117 others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | |||||||
| chr2:174367745 | TA | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0124 others(5): Show |
8 | HG00609.hp2 HG01069.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.484+11177delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367745 | |||||||
| chr2:174367752 | AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0116 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.484+11142_484+1117 others(33): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367752 | |||||||
| chr2:174367781 | TA | T | 9 | a0001c0001t0001g0026 a0001c0001t0002g0232 a0001c0001t0002g0233 others(6): Show |
9 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+11141delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367781 | |||||||
| chr2:174367830 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.484+11093T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367830 | |||||||
| chr2:174367843 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.484+11080A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367843 | |||||||
| chr2:174367884 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0223 |
2 | HG00733.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.484+11039C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174367884 | |||||||
| chr2:174368043 | A | G | 303 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(300): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.484+10880T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368043 | |||||||
| chr2:174368132 | T | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(171): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.484+10791A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368132 | |||||||
| chr2:174368164 | T | C | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(208): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.484+10759A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368164 | |||||||
| chr2:174368235 | TAATAG | T | 81 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(78): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.484+10683_484+1068 others(9): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368235 | |||||||
| chr2:174368355 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.484+10568C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368355 | |||||||
| chr2:174368545 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.484+10378C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368545 | |||||||
| chr2:174368548 | G | A | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+10375C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368548 | |||||||
| chr2:174368971 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.484+9952G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174368971 | |||||||
| chr2:174369087 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.484+9836A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369087 | |||||||
| chr2:174369107 | T | C | 13 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0049 others(10): Show |
16 | HG00735.hp1 HG01891.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.484+9816A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369107 | |||||||
| chr2:174369132 | T | C | 4 | a0002c0002t0003g0008 a0002c0002t0003g0230 a0002c0002t0003g0304 others(1): Show |
6 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+9791A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369132 | |||||||
| chr2:174369140 | A | C | 298 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(295): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.484+9783T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369140 | |||||||
| chr2:174369168 | CTGGAGAA others(21): Show |
C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+9727_484+9754d others(30): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369168 | |||||||
| chr2:174369489 | T | C | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+9434A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369489 | |||||||
| chr2:174369629 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.484+9294A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369629 | |||||||
| chr2:174369762 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.484+9161G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369762 | |||||||
| chr2:174369835 | A | C | 1 | a0001c0001t0002g0177 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.484+9088T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369835 | |||||||
| chr2:174369931 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.484+8992C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369931 | |||||||
| chr2:174369942 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.484+8981G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174369942 | |||||||
| chr2:174370123 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+8800C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370123 | |||||||
| chr2:174370164 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.484+8759C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370164 | |||||||
| chr2:174370264 | T | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+8659A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370264 | |||||||
| chr2:174370284 | G | C | 1 | a0002c0002t0003g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484+8639C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370284 | |||||||
| chr2:174370467 | A | G | 4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(1): Show |
4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+8456T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370467 | |||||||
| chr2:174370629 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(213): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.484+8294A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370629 | |||||||
| chr2:174370632 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.484+8291C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370632 | |||||||
| chr2:174370783 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.484+8140G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370783 | |||||||
| chr2:174370789 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+8134A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370789 | |||||||
| chr2:174370882 | T | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(214): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.484+8041A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370882 | |||||||
| chr2:174370910 | C | CA | 217 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(214): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.484+8012dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370910 | |||||||
| chr2:174370910 | CA | C | 33 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(30): Show |
35 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.484+8012delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370910 | |||||||
| chr2:174370921 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.484+8002T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370921 | |||||||
| chr2:174370944 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.484+7979G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370944 | |||||||
| chr2:174370970 | T | TCA | 3 | a0001c0001t0001g0017 a0001c0001t0001g0133 a0001c0001t0001g0138 |
4 | HG00558.hp1 NA18977.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+7951_484+7952d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370970 | |||||||
| chr2:174370995 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.484+7928C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174370995 | |||||||
| chr2:174371012 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+7911T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371012 | |||||||
| chr2:174371139 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.484+7784C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371139 | |||||||
| chr2:174371269 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.484+7654A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371269 | |||||||
| chr2:174371288 | G | A | 186 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(183): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.484+7635C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371288 | |||||||
| chr2:174371288 | G | T | 20 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(17): Show |
20 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+7635C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371288 | |||||||
| chr2:174371598 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.484+7325G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371598 | |||||||
| chr2:174371599 | C | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(88): Show |
100 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.484+7324G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174371599 | |||||||
| chr2:174372329 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.484+6594T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372329 | |||||||
| chr2:174372635 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.484+6288A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372635 | |||||||
| chr2:174372773 | G | C | 2 | a0001c0001t0002g0085 a0001c0001t0002g0189 |
2 | NA18942.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.484+6150C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174372773 | |||||||
| chr2:174373027 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0264 |
2 | HG01074.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.484+5896C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373027 | |||||||
| chr2:174373066 | A | C | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484+5857T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373066 | |||||||
| chr2:174373236 | C | T | 3 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 |
3 | HG02809.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.484+5687G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373236 | |||||||
| chr2:174373276 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0042 a0001c0001t0002g0045 others(1): Show |
5 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+5647T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373276 | |||||||
| chr2:174373299 | T | TA | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(167): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+5623dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373299 | |||||||
| chr2:174373448 | C | A | 14 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+5475G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373448 | |||||||
| chr2:174373689 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+5234A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373689 | |||||||
| chr2:174373764 | TA | T | 15 | a0001c0001t0001g0129 a0001c0001t0001g0138 a0001c0001t0001g0141 others(12): Show |
15 | HG00280.hp1 HG00558.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.484+5158delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373764 | |||||||
| chr2:174373828 | C | CTG | 18 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
18 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.484+5093_484+5094d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | |||||||
| chr2:174373828 | C | CTGTG | 16 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0106 others(13): Show |
20 | HG00735.hp1 HG02258.hp2 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+5091_484+5094d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | |||||||
| chr2:174373828 | CT | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(167): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+5094delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373828 | |||||||
| chr2:174373856 | T | TTTC | 298 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(295): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.484+5064_484+5066d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174373856 | |||||||
| chr2:174374019 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484+4904C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374019 | |||||||
| chr2:174374111 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.484+4812T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374111 | |||||||
| chr2:174374196 | T | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+4727A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374196 | |||||||
| chr2:174374346 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG01099.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.484+4577G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374346 | |||||||
| chr2:174374347 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.484+4576C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374347 | |||||||
| chr2:174374354 | T | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(76): Show |
84 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.484+4569A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374354 | |||||||
| chr2:174374457 | A | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(167): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+4466T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374457 | |||||||
| chr2:174374534 | CA | C | 7 | a0002c0002t0003g0012 a0002c0002t0003g0013 a0002c0002t0003g0043 others(4): Show |
9 | HG00735.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.484+4388delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374534 | |||||||
| chr2:174374597 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.484+4326G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374597 | |||||||
| chr2:174374730 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.484+4193A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374730 | |||||||
| chr2:174374790 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.484+4133T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174374790 | |||||||
| chr2:174375080 | A | G | 4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0177 others(1): Show |
4 | HG01074.hp2 HG03942.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+3843T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375080 | |||||||
| chr2:174375189 | A | T | 170 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(167): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.484+3734T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375189 | |||||||
| chr2:174375225 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0045 a0001c0001t0002g0117 |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+3698C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375225 | |||||||
| chr2:174375279 | A | G | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.484+3644T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375279 | |||||||
| chr2:174375425 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+3498A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375425 | |||||||
| chr2:174375564 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(166): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.484+3359G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375564 | |||||||
| chr2:174375761 | T | C | 75 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
77 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.484+3162A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375761 | |||||||
| chr2:174375890 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.484+3033C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174375890 | |||||||
| chr2:174376133 | T | C | 1 | a0001c0001t0002g0010 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.484+2790A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376133 | |||||||
| chr2:174376319 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.484+2604T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376319 | |||||||
| chr2:174376706 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484+2217C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376706 | |||||||
| chr2:174376729 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484+2194G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376729 | |||||||
| chr2:174376730 | G | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0205 a0001c0001t0001g0206 others(13): Show |
17 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+2193C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376730 | |||||||
| chr2:174376737 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0009g0281 |
2 | HG02698.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.484+2186C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376737 | |||||||
| chr2:174376754 | T | C | 125 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(122): Show |
133 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.484+2169A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376754 | |||||||
| chr2:174376801 | GA | G | 76 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0052 others(73): Show |
78 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.484+2121delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376801 | |||||||
| chr2:174376802 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.484+2121T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376802 | |||||||
| chr2:174376803 | A | G | 40 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(37): Show |
41 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.484+2120T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376803 | |||||||
| chr2:174376804 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0153 |
2 | HG02015.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.484+2119T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376804 | |||||||
| chr2:174376838 | G | A | 14 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0092 others(11): Show |
14 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.484+2085C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376838 | |||||||
| chr2:174376960 | C | G | 1 | a0002c0002t0003g0304 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.484+1963G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174376960 | |||||||
| chr2:174377353 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.484+1570C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377353 | |||||||
| chr2:174377376 | G | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
11 | HG00673.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.484+1547C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377376 | |||||||
| chr2:174377407 | G | T | 2 | a0001c0001t0002g0189 a0001c0001t0003g0201 |
2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.484+1516C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377407 | |||||||
| chr2:174377426 | T | C | 5 | a0001c0001t0002g0106 a0001c0001t0002g0202 a0001c0001t0002g0231 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+1497A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377426 | |||||||
| chr2:174377476 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484+1447T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377476 | |||||||
| chr2:174377539 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484+1384T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377539 | |||||||
| chr2:174377717 | C | T | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0139 others(2): Show |
5 | HG00738.hp2 HG01496.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.484+1206G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377717 | |||||||
| chr2:174377753 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.484+1170T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377753 | |||||||
| chr2:174377761 | G | C | 2 | a0001c0001t0002g0131 a0001c0001t0002g0197 |
2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.484+1162C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377761 | |||||||
| chr2:174377781 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.484+1142G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377781 | |||||||
| chr2:174377824 | C | CA | 73 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(70): Show |
84 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.484+1098dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | |||||||
| chr2:174377824 | C | CAA | 17 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0001g0196 others(14): Show |
17 | HG01106.hp2 HG01109.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+1097_484+1098d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | |||||||
| chr2:174377824 | C | CAAA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0099 a0001c0001t0001g0118 others(10): Show |
16 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.484+1096_484+1098d others(5): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | |||||||
| chr2:174377824 | C | CAAAA | 65 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0024 others(62): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.484+1095_484+1098d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | |||||||
| chr2:174377824 | C | CAAAAA | 40 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0090 others(37): Show |
42 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.484+1094_484+1098d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377824 | |||||||
| chr2:174377875 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(173): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.484+1048G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377875 | |||||||
| chr2:174377913 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(48): Show |
56 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.484+1010C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174377913 | |||||||
| chr2:174378113 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.484+810A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378113 | |||||||
| chr2:174378320 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.484+603C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378320 | |||||||
| chr2:174378496 | G | C | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
15 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.484+427C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378496 | |||||||
| chr2:174378523 | TTTG | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(100): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.484+397_484+399del others(3): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378523 | |||||||
| chr2:174378577 | C | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.484+346G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378577 | |||||||
| chr2:174378692 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.484+231C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378692 | |||||||
| chr2:174378693 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.484+230C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378693 | |||||||
| chr2:174378697 | T | G | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.484+226A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378697 | |||||||
| chr2:174378773 | T | C | 65 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(62): Show |
70 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.484+150A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378773 | |||||||
| chr2:174378796 | T | G | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.484+127A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 7/9 | chr2 | 174378796 | |||||||
| chr2:174379321 | C | T | 1 | a0003c0003t0001g0014 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-281G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379321 | |||||||
| chr2:174379394 | C | T | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.367-354G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379394 | |||||||
| chr2:174379473 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.367-433A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379473 | |||||||
| chr2:174379479 | C | A | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.367-439G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379479 | |||||||
| chr2:174379716 | C | CT | 35 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(32): Show |
36 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.366+485dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | |||||||
| chr2:174379716 | C | CTT | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG01517.hp2 HG02572.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+484_366+485dup others(2): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | |||||||
| chr2:174379716 | CT | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(127): Show |
153 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.366+485delA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | |||||||
| chr2:174379716 | CTTTT | C | 13 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(10): Show |
13 | HG00140.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.366+482_366+485del others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379716 | |||||||
| chr2:174379739 | T | A | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.366+463A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379739 | |||||||
| chr2:174379754 | C | T | 46 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(43): Show |
50 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.366+448G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379754 | |||||||
| chr2:174379809 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.366+393G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379809 | |||||||
| chr2:174379869 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.366+333C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174379869 | |||||||
| chr2:174380028 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(289): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.366+174A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 6/9 | chr2 | 174380028 | |||||||
| chr2:174380344 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.318-94T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380344 | |||||||
| chr2:174380443 | T | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.318-193A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380443 | |||||||
| chr2:174380514 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(35): Show |
42 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.317+137T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 5/9 | chr2 | 174380514 | |||||||
| chr2:174380899 | TATC | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(100): Show |
114 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.242-88_242-86delGA others(1): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380899 | |||||||
| chr2:174380980 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.242-166A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380980 | |||||||
| chr2:174380986 | G | A | 1 | a0001c0001t0002g0020 | 2 | NA18983.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.242-172C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174380986 | |||||||
| chr2:174381016 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.242-202A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381016 | |||||||
| chr2:174381045 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.242-231A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381045 | |||||||
| chr2:174381101 | A | G | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.242-287T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381101 | |||||||
| chr2:174381102 | A | G | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.242-288T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381102 | |||||||
| chr2:174381330 | G | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(223): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.241+374C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 3/9 | chr2 | 174381330 | |||||||
| chr2:174382195 | T | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(109): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.168-418A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382195 | |||||||
| chr2:174382325 | G | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-548C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382325 | |||||||
| chr2:174382362 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.168-585C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382362 | |||||||
| chr2:174382393 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.168-616G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382393 | |||||||
| chr2:174382510 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.168-733C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382510 | |||||||
| chr2:174382567 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-790T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382567 | |||||||
| chr2:174382587 | C | T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0197 |
3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-810G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382587 | |||||||
| chr2:174382650 | T | C | 299 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(296): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.168-873A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382650 | |||||||
| chr2:174382794 | G | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-1017C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382794 | |||||||
| chr2:174382972 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(105): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.168-1195A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174382972 | |||||||
| chr2:174383038 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02698.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.168-1261T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383038 | |||||||
| chr2:174383312 | T | G | 1 | a0001c0001t0002g0085 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.168-1535A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383312 | |||||||
| chr2:174383366 | TAAAAA | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.168-1594_168-1590d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383366 | |||||||
| chr2:174383548 | C | T | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-1771G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383548 | |||||||
| chr2:174383632 | A | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.168-1855T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383632 | |||||||
| chr2:174383668 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168-1891G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383668 | |||||||
| chr2:174383677 | A | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(171): Show |
190 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.168-1900T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383677 | |||||||
| chr2:174383701 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.168-1924A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383701 | |||||||
| chr2:174383711 | C | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0034 |
2 | HG01934.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.168-1934G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383711 | |||||||
| chr2:174383719 | C | CA | 17 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-1943dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | |||||||
| chr2:174383719 | CA | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(147): Show |
166 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.168-1943delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | |||||||
| chr2:174383719 | CAA | C | 10 | a0001c0001t0001g0234 a0001c0001t0002g0232 a0001c0001t0002g0233 others(7): Show |
10 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1944_168-1943d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383719 | |||||||
| chr2:174383835 | GGCTA | G | 2 | a0001c0001t0002g0018 a0001c0001t0002g0175 |
3 | HG02055.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-2062_168-2059d others(6): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383835 | |||||||
| chr2:174383849 | C | CA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(57): Show |
67 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.168-2073dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | |||||||
| chr2:174383849 | C | CAA | 11 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(8): Show |
11 | HG01109.hp1 HG01192.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.168-2074_168-2073d others(4): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | |||||||
| chr2:174383849 | CAAAAA | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0199 a0001c0001t0002g0200 |
6 | HG01891.hp1 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2077_168-2073d others(7): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | |||||||
| chr2:174383849 | CAAAAAA | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
116 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.168-2078_168-2073d others(8): Show |
CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383849 | |||||||
| chr2:174383894 | T | G | 2 | a0001c0001t0003g0201 a0002c0002t0003g0043 |
2 | HG02647.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.168-2117A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174383894 | |||||||
| chr2:174384067 | A | G | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.168-2290T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384067 | |||||||
| chr2:174384162 | G | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG02015.hp1 HG02040.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-2385C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384162 | |||||||
| chr2:174384482 | C | A | 2 | a0001c0001t0002g0105 a0001c0001t0002g0107 |
2 | HG03942.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.168-2705G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384482 | |||||||
| chr2:174384542 | A | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-2765T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384542 | |||||||
| chr2:174384607 | T | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.168-2830A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384607 | |||||||
| chr2:174384715 | C | T | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.168-2938G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384715 | |||||||
| chr2:174384741 | T | A | 127 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(124): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.167+2944A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384741 | |||||||
| chr2:174384952 | G | A | 4 | a0001c0001t0002g0216 a0001c0001t0002g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG00642.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+2733C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174384952 | |||||||
| chr2:174385215 | C | CA | 8 | a0001c0001t0001g0114 a0001c0001t0001g0196 a0001c0001t0001g0267 others(5): Show |
8 | HG01106.hp2 HG02080.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+2469dupT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385215 | |||||||
| chr2:174385215 | CA | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(148): Show |
167 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.167+2469delT | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385215 | |||||||
| chr2:174385225 | A | C | 1 | a0001c0001t0002g0005 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.167+2460T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385225 | |||||||
| chr2:174385233 | A | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(146): Show |
164 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.167+2452T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385233 | |||||||
| chr2:174385437 | C | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(169): Show |
188 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.167+2248G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385437 | |||||||
| chr2:174385502 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.167+2183C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385502 | |||||||
| chr2:174385561 | T | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(169): Show |
188 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.167+2124A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385561 | |||||||
| chr2:174385672 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.167+2013C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385672 | |||||||
| chr2:174385722 | A | T | 2 | a0001c0001t0001g0125 a0005c0007t0001g0126 |
2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.167+1963T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385722 | |||||||
| chr2:174385743 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167+1942A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385743 | |||||||
| chr2:174385753 | A | G | 2 | a0001c0001t0001g0125 a0005c0007t0001g0126 |
2 | HG01952.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.167+1932T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385753 | |||||||
| chr2:174385810 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.167+1875A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385810 | |||||||
| chr2:174385833 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.167+1852G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385833 | |||||||
| chr2:174385958 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.167+1727A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385958 | |||||||
| chr2:174385973 | G | C | 1 | a0001c0001t0002g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.167+1712C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174385973 | |||||||
| chr2:174386011 | A | T | 1 | a0001c0001t0002g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.167+1674T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386011 | |||||||
| chr2:174386147 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.167+1538C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386147 | |||||||
| chr2:174386212 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(33): Show |
40 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.167+1473C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386212 | |||||||
| chr2:174386254 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.167+1431A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386254 | |||||||
| chr2:174386257 | G | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(170): Show |
189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.167+1428C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386257 | |||||||
| chr2:174386293 | T | C | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.167+1392A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386293 | |||||||
| chr2:174386328 | T | G | 1 | a0001c0001t0001g0296 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.167+1357A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386328 | |||||||
| chr2:174386418 | G | A | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.167+1267C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386418 | |||||||
| chr2:174386474 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.167+1211C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386474 | |||||||
| chr2:174386586 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.167+1099C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386586 | |||||||
| chr2:174386707 | A | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.167+978T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386707 | |||||||
| chr2:174386892 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.167+793A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174386892 | |||||||
| chr2:174387099 | G | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(170): Show |
189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.167+586C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387099 | |||||||
| chr2:174387114 | T | C | 1 | a0001c0001t0001g0297 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.167+571A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387114 | |||||||
| chr2:174387310 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.167+375G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387310 | |||||||
| chr2:174387320 | A | T | 5 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | HG00673.hp2 NA18945.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+365T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387320 | |||||||
| chr2:174387522 | T | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.167+163A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 2/9 | chr2 | 174387522 | |||||||
| chr2:174387803 | A | G | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-24T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174387803 | |||||||
| chr2:174387944 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.73-165C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174387944 | |||||||
| chr2:174388157 | C | T | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-378G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388157 | |||||||
| chr2:174388263 | A | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-484T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388263 | |||||||
| chr2:174388322 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.73-543G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388322 | |||||||
| chr2:174388525 | G | T | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.73-746C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388525 | |||||||
| chr2:174388544 | T | A | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-765A>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388544 | |||||||
| chr2:174388700 | C | A | 4 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0006g0222 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-921G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388700 | |||||||
| chr2:174388703 | G | A | 2 | a0001c0001t0001g0298 a0007c0006t0001g0299 |
2 | NA19004.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.73-924C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388703 | |||||||
| chr2:174388766 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.73-987G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388766 | |||||||
| chr2:174388790 | C | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-1011G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388790 | |||||||
| chr2:174388829 | G | A | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG03704.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.73-1050C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388829 | |||||||
| chr2:174388849 | T | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0172 a0001c0001t0002g0199 others(1): Show |
7 | HG01891.hp1 HG02257.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1070A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388849 | |||||||
| chr2:174388998 | A | G | 1 | a0001c0001t0002g0101 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-1219T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174388998 | |||||||
| chr2:174389096 | A | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(219): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.73-1317T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389096 | |||||||
| chr2:174389137 | G | A | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-1358C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389137 | |||||||
| chr2:174389255 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-1476T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389255 | |||||||
| chr2:174389299 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(221): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.73-1520A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389299 | |||||||
| chr2:174389354 | G | C | 1 | a0001c0001t0007g0170 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.73-1575C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389354 | |||||||
| chr2:174389473 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(32): Show |
39 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-1694A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389473 | |||||||
| chr2:174389556 | G | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(223): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.73-1777C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389556 | |||||||
| chr2:174389645 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 |
3 | HG02615.hp2 HG02895.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.73-1866G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389645 | |||||||
| chr2:174389690 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-1911C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389690 | |||||||
| chr2:174389700 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.73-1921G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389700 | |||||||
| chr2:174389714 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0302 |
3 | NA18954.hp1 NA18991.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.73-1935C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389714 | |||||||
| chr2:174389783 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(32): Show |
39 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.73-2004A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389783 | |||||||
| chr2:174389792 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.73-2013C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389792 | |||||||
| chr2:174389844 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.73-2065C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389844 | |||||||
| chr2:174389867 | T | G | 115 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(112): Show |
126 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.73-2088A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174389867 | |||||||
| chr2:174390031 | T | C | 63 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(60): Show |
68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.73-2252A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390031 | |||||||
| chr2:174390087 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(223): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.73-2308G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390087 | |||||||
| chr2:174390145 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-2366A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390145 | |||||||
| chr2:174390225 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.73-2446C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390225 | |||||||
| chr2:174390239 | A | G | 12 | a0001c0001t0002g0011 a0001c0001t0002g0055 a0001c0001t0002g0057 others(9): Show |
15 | HG00735.hp1 HG01884.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.73-2460T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390239 | |||||||
| chr2:174390290 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-2511C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390290 | |||||||
| chr2:174390358 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.73-2579C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390358 | |||||||
| chr2:174390470 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.73-2691T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390470 | |||||||
| chr2:174390690 | G | GT | 71 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(68): Show |
76 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.73-2912dupA | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390690 | |||||||
| chr2:174390731 | G | A | 6 | a0001c0001t0002g0042 a0001c0001t0002g0108 a0001c0001t0002g0117 others(3): Show |
6 | HG02257.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-2952C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390731 | |||||||
| chr2:174390756 | G | A | 1 | a0001c0001t0008g0028 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.73-2977C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390756 | |||||||
| chr2:174390959 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.73-3180T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174390959 | |||||||
| chr2:174391040 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.73-3261T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391040 | |||||||
| chr2:174391213 | T | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0246 a0001c0001t0001g0247 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.73-3434A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391213 | |||||||
| chr2:174391255 | G | A | 24 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(21): Show |
29 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.73-3476C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391255 | |||||||
| chr2:174391734 | A | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02080.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.72+3817T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391734 | |||||||
| chr2:174391791 | G | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.72+3760C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391791 | |||||||
| chr2:174391882 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+3669A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391882 | |||||||
| chr2:174391944 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+3607G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174391944 | |||||||
| chr2:174392059 | G | A | 5 | a0001c0001t0002g0225 a0001c0001t0002g0226 a0001c0001t0002g0227 others(2): Show |
5 | HG00673.hp2 NA18945.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+3492C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392059 | |||||||
| chr2:174392142 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(1): Show |
4 | HG02738.hp1 NA18945.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+3409G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392142 | |||||||
| chr2:174392401 | T | C | 6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG03704.hp2 HG03834.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+3150A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392401 | |||||||
| chr2:174392563 | G | C | 2 | a0002c0002t0003g0008 a0002c0002t0003g0230 |
4 | HG02630.hp1 HG02896.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2988C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392563 | |||||||
| chr2:174392611 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.72+2940C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392611 | |||||||
| chr2:174392791 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72+2760A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392791 | |||||||
| chr2:174392915 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0005g0115 a0001c0001t0005g0270 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2636C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392915 | |||||||
| chr2:174392948 | G | T | 1 | a0001c0001t0002g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.72+2603C>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174392948 | |||||||
| chr2:174393206 | G | C | 9 | a0001c0001t0001g0234 a0001c0001t0002g0232 a0001c0001t0002g0233 others(6): Show |
9 | HG00735.hp2 HG01070.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+2345C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393206 | |||||||
| chr2:174393212 | T | G | 5 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(2): Show |
6 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2339A>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393212 | |||||||
| chr2:174393405 | C | A | 3 | a0001c0001t0005g0115 a0001c0001t0005g0270 a0001c0001t0005g0271 |
3 | HG02896.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.72+2146G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393405 | |||||||
| chr2:174393534 | TG | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0002g0047 others(1): Show |
7 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+2016delC | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393534 | |||||||
| chr2:174393556 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72+1995A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393556 | |||||||
| chr2:174393691 | A | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0106 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.72+1860T>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174393691 | |||||||
| chr2:174394166 | A | G | 2 | a0001c0001t0002g0010 a0001c0001t0002g0045 |
3 | HG02965.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.72+1385T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394166 | |||||||
| chr2:174394198 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.72+1353A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394198 | |||||||
| chr2:174394337 | A | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0046 others(105): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.72+1214T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394337 | |||||||
| chr2:174394375 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+1176T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394375 | |||||||
| chr2:174394479 | C | A | 1 | a0001c0001t0008g0028 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.72+1072G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394479 | |||||||
| chr2:174394688 | G | C | 25 | a0001c0001t0001g0023 a0001c0001t0001g0246 a0001c0001t0001g0247 others(22): Show |
26 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.72+863C>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394688 | |||||||
| chr2:174394696 | G | A | 2 | a0001c0001t0005g0270 a0001c0001t0005g0271 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.72+855C>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394696 | |||||||
| chr2:174394995 | C | T | 1 | a0002c0002t0003g0043 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+556G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174394995 | |||||||
| chr2:174395074 | A | G | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.72+477T>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395074 | |||||||
| chr2:174395163 | A | C | 1 | a0001c0001t0002g0042 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+388T>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395163 | |||||||
| chr2:174395282 | T | C | 37 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(34): Show |
41 | HG00408.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.72+269A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395282 | |||||||
| chr2:174395311 | T | C | 2 | a0002c0002t0003g0304 a0002c0002t0003g0305 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.72+240A>G | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395311 | |||||||
| chr2:174395380 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.72+171G>C | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395380 | |||||||
| chr2:174395486 | C | A | 1 | a0001c0001t0001g0306 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.72+65G>T | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395486 | |||||||
| chr2:174395496 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0036 a0001c0001t0002g0037 others(3): Show |
7 | NA18954.hp2 NA18963.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+55G>A | CIR1 | ENSG00000138433.16 | transcript | ENST00000342016.8 | protein_coding | 1/9 | chr2 | 174395496 |