Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9702 |
| ensemblid | ENSG00000166037.11 |
| hgncid | 30794 |
| symbol | CEP57 |
| name | centrosomal protein 57 |
| refseq_nuc | NM_014679.5 |
| refseq_prot | NP_055494.2 |
| ensembl_nuc | ENST00000325542.10 |
| ensembl_prot | ENSP00000317902.5 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 95790498 |
| end | 95832693 |
| strand | + |
| ver | v1.2 |
| region | chr11:95790498-95832693 |
| region5000 | chr11:95785498-95837693 |
| regionname0 | CEP57_chr11_95790498_95832693 |
| regionname5000 | CEP57_chr11_95785498_95837693 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 500 | 247 | 79 | 40 | 86 | 11 | 30 | 69 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(495): Show |
chr11 | 95785498 | 95837693 |
| a0002 | 0/1 | 500 | 89 | 10 | 14 | 53 | 5 | 6 | 42 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(495): Show |
chr11 | 95785498 | 95837693 |
| a0003 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(495): Show |
chr11 | 95785498 | 95837693 |
| a0004 | 0/0 | 361 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(356): Show |
chr11 | 95785498 | 95837693 |
| a0005 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(495): Show |
chr11 | 95785498 | 95837693 |
| a0006 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | MAAAS others(495): Show |
chr11 | 95785498 | 95837693 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1500 | 242 | 77 | 38 | 85 | 11 | 30 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0001c0003 | 0/0 | 1500 | 3 | 1 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0001c0006 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0001c0011 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0002c0002 | 0/1 | 1500 | 87 | 10 | 13 | 52 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0002c0004 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0002c0007 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0003c0005 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0004c0009 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0005c0010 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 | ||
| a0006c0008 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | ATGGC others(1495): Show |
chr11 | 95785498 | 95837693 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3141 | 124 | 12 | 25 | 62 | 10 | 14 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0003 | 0/0 | 3141 | 58 | 36 | 10 | 8 | 1 | 3 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0004 | 0/0 | 3141 | 21 | 20 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0005 | 0/0 | 3141 | 18 | 2 | 1 | 14 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0006 | 0/0 | 3141 | 7 | 0 | 0 | 1 | 0 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0007 | 0/0 | 3141 | 6 | 0 | 1 | 0 | 0 | 5 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0008 | 0/0 | 3141 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | TTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0009 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0011 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0012 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0001t0013 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0003t0005 | 0/0 | 3141 | 3 | 1 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0006t0003 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0001c0011t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0002c0002t0002 | 0/0 | 3140 | 85 | 9 | 13 | 52 | 5 | 6 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3135): Show |
chr11 | 95785498 | 95837693 |
| a0002c0002t0004 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0002c0002t0010 | 0/1 | 3140 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3135): Show |
chr11 | 95785498 | 95837693 |
| a0002c0004t0002 | 0/0 | 3140 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3135): Show |
chr11 | 95785498 | 95837693 |
| a0002c0007t0002 | 0/0 | 3140 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3135): Show |
chr11 | 95785498 | 95837693 |
| a0003c0005t0003 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0004c0009t0001 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0005c0010t0003 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| a0006c0008t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | CTTTC others(3136): Show |
chr11 | 95785498 | 95837693 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 4 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0001 | 0/0 | 17 | 9 | 3 | 3 | 1 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0001t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0003t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0003t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0006t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0001c0011t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0002t0010g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0002c0007t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0003c0005t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0004c0009t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0005c0010t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| a0006c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | GBR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0038 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0197 | EUR | FIN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0182 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0216 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01167 | hp1 | a0001 | c0003 | t0005 | g0251 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01169 | hp1 | a0001 | c0003 | t0005 | g0252 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01175 | hp2 | a0002 | c0007 | t0002 | g0225 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0212 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0183 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01361 | hp1 | a0003 | c0005 | t0003 | g0138 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01981 | hp2 | a0004 | c0009 | t0001 | g0088 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0233 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | KHV | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0220 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0237 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0129 | AMR | PEL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0238 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0227 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0217 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02738 | hp1 | a0001 | c0001 | t0013 | g0102 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02886 | hp2 | a0001 | c0006 | t0003 | g0148 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0191 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0235 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03139 | hp2 | a0005 | c0010 | t0003 | g0001 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0177 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03239 | hp1 | a0001 | c0001 | t0007 | g0127 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0223 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0134 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0049 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0133 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0181 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0241 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0137 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0132 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0130 | SAS | STU | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | CHB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0232 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0247 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18969 | hp2 | a0001 | c0011 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18987 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19009 | hp1 | a0006 | c0008 | t0001 | g0008 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19074 | hp1 | a0002 | c0004 | t0002 | g0017 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0230 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | YRI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0250 | AFR | ASW | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0192 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0048 | SAS | GIH | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | USA | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0226 | AFR | LWK | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0010 | g0045 | REF | REF | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0052 | REF | REF | CEP57_chr11_95785498_95837693 | CEP57 | chr11 | 95785498 | 95837693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95813062 | G | C | 1 | a0003 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.333G>C | p.Gln111His | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 3/11 | 534/3141 | 333/1503 | 111/500 | chr11 | 95813062 | |||
| chr11:95827879 | A | G | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.979A>G | p.Ile327Val | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1180/3141 | 979/1503 | 327/500 | chr11 | 95827879 | |||
| chr11:95827963 | G | A | 1 | a0006 | 1 | NA19009.hp1 | missense_variant | MODERATE | c.1063G>A | p.Gly355Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1264/3141 | 1063/1503 | 355/500 | chr11 | 95827963 | |||
| chr11:95827981 | T | G | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1081T>G | p.Ser361Ala | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1282/3141 | 1081/1503 | 361/500 | chr11 | 95827981 | |||
| chr11:95827982 | C | A | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1082C>A | p.Ser361* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1283/3141 | 1082/1503 | 361/500 | chr11 | 95827982 | |||
| chr11:95827984 | G | T | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1084G>T | p.Glu362* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1285/3141 | 1084/1503 | 362/500 | chr11 | 95827984 | |||
| chr11:95827987 | G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1087G>C | p.Val363Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1288/3141 | 1087/1503 | 363/500 | chr11 | 95827987 | |||
| chr11:95827991 | T | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1091T>C | p.Leu364Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1292/3141 | 1091/1503 | 364/500 | chr11 | 95827991 | |||
| chr11:95827992 | A | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1092A>C | p.Leu364Phe | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1293/3141 | 1092/1503 | 364/500 | chr11 | 95827992 | |||
| chr11:95827994 | A | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1094A>T | p.Gln365Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1295/3141 | 1094/1503 | 365/500 | chr11 | 95827994 | |||
| chr11:95828000 | T | G | 1 | a0004 | 1 | HG01981.hp2 | stop_gained | HIGH | c.1100T>G | p.Leu367* | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1301/3141 | 1100/1503 | 367/500 | chr11 | 95828000 | |||
| chr11:95828003 | A | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1103A>T | p.Gln368Leu | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1304/3141 | 1103/1503 | 368/500 | chr11 | 95828003 | |||
| chr11:95828004 | G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1104G>C | p.Gln368His | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1305/3141 | 1104/1503 | 368/500 | chr11 | 95828004 | |||
| chr11:95828008 | G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1108G>C | p.Glu370Gln | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1309/3141 | 1108/1503 | 370/500 | chr11 | 95828008 | |||
| chr11:95828015 | G | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1115G>C | p.Gly372Ala | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1316/3141 | 1115/1503 | 372/500 | chr11 | 95828015 | |||
| chr11:95828023 | A | C | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1123A>C | p.Ser375Arg | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1324/3141 | 1123/1503 | 375/500 | chr11 | 95828023 | |||
| chr11:95828024 | G | T | 1 | a0004 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1124G>T | p.Ser375Ile | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1325/3141 | 1124/1503 | 375/500 | chr11 | 95828024 | |||
| chr11:95831095 | A | G | 1 | a0002 | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
missense_variant | MODERATE | c.1342A>G | p.Arg448Gly | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1543/3141 | 1342/1503 | 448/500 | chr11 | 95831095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95799309 | G | A | 1 | a0002c0004 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.123G>A | p.Ser41Ser | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/11 | 324/3141 | 123/1503 | 41/500 | chr11 | 95799309 | |||
| chr11:95818838 | A | G | 1 | a0001c0011 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.633A>G | p.Gln211Gln | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/11 | 834/3141 | 633/1503 | 211/500 | chr11 | 95818838 | |||
| chr11:95821924 | G | A | 2 | a0001c0006 a0002c0007 |
2 | HG01175.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.753G>A | p.Pro251Pro | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/11 | 954/3141 | 753/1503 | 251/500 | chr11 | 95821924 | |||
| chr11:95821969 | A | G | 1 | a0001c0003 | 3 | HG01167.hp1 HG01169.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.798A>G | p.Pro266Pro | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/11 | 999/3141 | 798/1503 | 266/500 | chr11 | 95821969 | |||
| chr11:95828016 | G | A | 1 | a0004c0009 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.1116G>A | p.Gly372Gly | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/11 | 1317/3141 | 1116/1503 | 372/500 | chr11 | 95828016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95790498 | C | T | 1 | a0001c0001t0008 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-201C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 201 | chr11 | 95790498 | ||||||
| chr11:95790577 | G | A | 1 | a0001c0001t0006 | 7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-122G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 122 | chr11 | 95790577 | ||||||
| chr11:95790646 | A | G | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0003t0005 |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-53A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 53 | chr11 | 95790646 | ||||||
| chr11:95790671 | T | C | 1 | a0001c0001t0007 | 6 | HG02300.hp2 HG02735.hp1 HG03239.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 28 | chr11 | 95790671 | ||||||
| chr11:95790684 | T | G | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/11 | 15 | chr11 | 95790684 | ||||||
| chr11:95831628 | A | T | 1 | a0001c0001t0013 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 372 | chr11 | 95831628 | ||||||
| chr11:95832047 | A | G | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*791A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 791 | chr11 | 95832047 | ||||||
| chr11:95832124 | A | G | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(10): Show |
196 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*868A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 868 | chr11 | 95832124 | ||||||
| chr11:95832444 | TA | T | 3 | a0002c0002t0002 a0002c0004t0002 a0002c0007t0002 |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1190delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1190 | INFO_REALIGN_3_PRIME | chr11 | 95832444 | |||||
| chr11:95832617 | C | A | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1361 | chr11 | 95832617 | ||||||
| chr11:95832625 | G | A | 3 | a0002c0002t0002 a0002c0004t0002 a0002c0007t0002 |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1369G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1369 | chr11 | 95832625 | ||||||
| chr11:95832676 | G | A | 4 | a0001c0001t0003 a0001c0006t0003 a0003c0005t0003 others(1): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1420G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 11/11 | 1420 | chr11 | 95832676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:95790808 | G | A | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+65G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790808 | |||||||
| chr11:95790818 | G | A | 2 | a0002c0002t0002g0042 a0002c0002t0002g0043 |
2 | HG00438.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.45+75G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790818 | |||||||
| chr11:95790863 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+120G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790863 | |||||||
| chr11:95790903 | G | T | 97 | a0001c0001t0001g0173 a0001c0001t0005g0039 a0001c0001t0005g0040 others(94): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.45+160G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790903 | |||||||
| chr11:95790969 | C | T | 24 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0005g0039 others(21): Show |
26 | HG01081.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.45+226C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95790969 | |||||||
| chr11:95791221 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45+478C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791221 | |||||||
| chr11:95791257 | G | A | 97 | a0001c0001t0001g0173 a0001c0001t0005g0039 a0001c0001t0005g0040 others(94): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.45+514G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791257 | |||||||
| chr11:95791432 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.45+689C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791432 | |||||||
| chr11:95791549 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
8 | HG00609.hp2 HG00621.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+806A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791549 | |||||||
| chr11:95791555 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.45+812C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791555 | |||||||
| chr11:95791681 | A | T | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.45+938A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791681 | |||||||
| chr11:95791694 | G | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(30): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.45+951G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95791694 | |||||||
| chr11:95792228 | GC | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0047 |
4 | HG01515.hp1 HG01517.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+1486delC | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792228 | |||||||
| chr11:95792284 | C | A | 1 | a0001c0001t0006g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.45+1541C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792284 | |||||||
| chr11:95792502 | G | A | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+1759G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792502 | |||||||
| chr11:95792639 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.45+1896T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792639 | |||||||
| chr11:95792689 | C | G | 1 | a0001c0001t0006g0137 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.45+1946C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792689 | |||||||
| chr11:95792708 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+1965A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792708 | |||||||
| chr11:95792757 | G | A | 1 | a0001c0001t0005g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.45+2014G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792757 | |||||||
| chr11:95792759 | A | T | 3 | a0001c0003t0005g0250 a0001c0003t0005g0251 a0001c0003t0005g0252 |
3 | HG01167.hp1 HG01169.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.45+2016A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792759 | |||||||
| chr11:95792792 | T | C | 1 | a0003c0005t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+2049T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792792 | |||||||
| chr11:95792922 | T | TA | 93 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(90): Show |
109 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.45+2192dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95792922 | ||||||
| chr11:95792953 | A | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.45+2210A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95792953 | |||||||
| chr11:95793083 | A | C | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2340A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793083 | |||||||
| chr11:95793234 | T | A | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.45+2491T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793234 | |||||||
| chr11:95793416 | T | TTA | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.45+2673_45+2674ins others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793416 | |||||||
| chr11:95793424 | C | T | 5 | a0002c0002t0002g0224 a0002c0002t0002g0226 a0002c0002t0002g0227 others(2): Show |
5 | HG01175.hp2 HG01891.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+2681C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793424 | |||||||
| chr11:95793551 | C | CTT | 164 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(161): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.45+2809_45+2810ins others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95793551 | ||||||
| chr11:95793731 | G | C | 1 | a0002c0002t0002g0174 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.45+2988G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793731 | |||||||
| chr11:95793761 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.45+3018A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793761 | |||||||
| chr11:95793788 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+3045A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793788 | |||||||
| chr11:95793795 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.45+3052T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793795 | |||||||
| chr11:95793822 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.45+3079G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95793822 | |||||||
| chr11:95794046 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.45+3303A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794046 | |||||||
| chr11:95794097 | G | A | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.45+3354G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794097 | |||||||
| chr11:95794213 | T | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0140 a0001c0001t0003g0141 |
6 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+3470T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794213 | |||||||
| chr11:95794329 | A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45+3586A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794329 | |||||||
| chr11:95794361 | T | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.45+3618T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794361 | |||||||
| chr11:95794487 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+3744G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794487 | |||||||
| chr11:95794569 | A | AGT | 3 | a0001c0001t0004g0114 a0002c0002t0002g0175 a0002c0002t0002g0176 |
3 | HG02040.hp2 HG02055.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.45+3841_45+3842dup others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95794569 | ||||||
| chr11:95794763 | A | G | 1 | a0003c0005t0003g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+4020A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794763 | |||||||
| chr11:95794881 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.45+4138G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794881 | |||||||
| chr11:95794980 | G | T | 2 | a0001c0003t0005g0251 a0001c0003t0005g0252 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.45+4237G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95794980 | |||||||
| chr11:95795043 | G | A | 1 | a0002c0002t0002g0175 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.46-4189G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795043 | |||||||
| chr11:95795045 | G | A | 72 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(69): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.46-4187G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795045 | |||||||
| chr11:95795060 | C | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-4172C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795060 | |||||||
| chr11:95795346 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.46-3886T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795346 | |||||||
| chr11:95795369 | ACT | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
7 | HG00423.hp1 NA18940.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3860_46-3859del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795369 | ||||||
| chr11:95795462 | T | C | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.46-3770T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795462 | |||||||
| chr11:95795484 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.46-3748T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795484 | |||||||
| chr11:95795499 | C | CT | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.46-3722dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795499 | ||||||
| chr11:95795499 | C | CTT | 5 | a0002c0002t0002g0038 a0002c0002t0002g0219 a0002c0002t0002g0220 others(2): Show |
6 | HG00280.hp2 HG00639.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-3723_46-3722dup others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 95795499 | ||||||
| chr11:95795550 | C | T | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.46-3682C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795550 | |||||||
| chr11:95795578 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.46-3654C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795578 | |||||||
| chr11:95795727 | G | T | 20 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0028 others(17): Show |
43 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.46-3505G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795727 | |||||||
| chr11:95795842 | CAT | C | 16 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(13): Show |
18 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.46-3389_46-3388del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795842 | |||||||
| chr11:95795858 | C | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-3374C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795858 | |||||||
| chr11:95795900 | A | C | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-3332A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95795900 | |||||||
| chr11:95796048 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.46-3184C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796048 | |||||||
| chr11:95796078 | T | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.46-3154T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796078 | |||||||
| chr11:95796237 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.46-2995T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796237 | |||||||
| chr11:95796427 | C | T | 16 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0069 others(13): Show |
18 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.46-2805C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796427 | |||||||
| chr11:95796961 | C | G | 72 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(69): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.46-2271C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796961 | |||||||
| chr11:95796990 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-2242A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95796990 | |||||||
| chr11:95797101 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.46-2131C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797101 | |||||||
| chr11:95797130 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.46-2102C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797130 | |||||||
| chr11:95797189 | C | T | 1 | a0001c0001t0005g0249 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.46-2043C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797189 | |||||||
| chr11:95797200 | T | A | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-2032T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797200 | |||||||
| chr11:95797272 | T | G | 1 | a0001c0001t0003g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46-1960T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797272 | |||||||
| chr11:95797365 | A | T | 2 | a0002c0002t0002g0217 a0002c0002t0002g0218 |
2 | HG00741.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.46-1867A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797365 | |||||||
| chr11:95797703 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(43): Show |
80 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.46-1529A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797703 | |||||||
| chr11:95797723 | T | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG00544.hp1 HG00621.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-1509T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797723 | |||||||
| chr11:95797745 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-1487A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797745 | |||||||
| chr11:95797901 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.46-1331A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95797901 | |||||||
| chr11:95798487 | A | G | 1 | a0001c0001t0005g0249 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.46-745A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798487 | |||||||
| chr11:95798555 | A | C | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.46-677A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798555 | |||||||
| chr11:95798584 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.46-648G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95798584 | |||||||
| chr11:95799002 | A | G | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.46-230A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 1/10 | chr11 | 95799002 | |||||||
| chr11:95799631 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+243A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799631 | |||||||
| chr11:95799676 | A | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+288A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799676 | |||||||
| chr11:95799753 | A | G | 1 | a0002c0002t0002g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.202+365A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95799753 | |||||||
| chr11:95800028 | G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.202+640G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800028 | |||||||
| chr11:95800038 | C | T | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+650C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800038 | |||||||
| chr11:95800136 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.202+748G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800136 | |||||||
| chr11:95800383 | C | CT | 10 | a0001c0001t0003g0007 a0001c0001t0003g0140 a0001c0001t0003g0141 others(7): Show |
14 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+1007dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95800383 | ||||||
| chr11:95800393 | T | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+1005T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800393 | |||||||
| chr11:95800402 | T | C | 1 | a0001c0003t0005g0250 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+1014T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800402 | |||||||
| chr11:95800463 | C | T | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.202+1075C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800463 | |||||||
| chr11:95800500 | A | G | 3 | a0002c0002t0002g0213 a0002c0002t0002g0214 a0002c0002t0002g0215 |
3 | NA18969.hp1 NA19063.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.202+1112A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800500 | |||||||
| chr11:95800748 | G | A | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+1360G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800748 | |||||||
| chr11:95800763 | GGTTAT | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+1381_202+1385d others(7): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95800763 | ||||||
| chr11:95800992 | T | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG01167.hp2 HG01192.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.202+1604T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95800992 | |||||||
| chr11:95801012 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+1624A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801012 | |||||||
| chr11:95801080 | G | T | 16 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0069 others(13): Show |
18 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.202+1692G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801080 | |||||||
| chr11:95801248 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.202+1860G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801248 | |||||||
| chr11:95801276 | T | G | 2 | a0002c0002t0002g0177 a0002c0002t0002g0178 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.202+1888T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801276 | |||||||
| chr11:95801277 | G | A | 164 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(161): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.202+1889G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801277 | |||||||
| chr11:95801289 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.202+1901C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801289 | |||||||
| chr11:95801297 | C | T | 3 | a0001c0001t0005g0247 a0001c0001t0005g0248 a0001c0001t0005g0249 |
3 | NA18946.hp2 NA18979.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.202+1909C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801297 | |||||||
| chr11:95801316 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.202+1928G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801316 | |||||||
| chr11:95801324 | A | T | 1 | a0002c0002t0002g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.202+1936A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801324 | |||||||
| chr11:95801450 | C | CA | 50 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0108 others(47): Show |
62 | HG00423.hp2 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.202+2081dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | ||||||
| chr11:95801450 | C | CAA | 7 | a0001c0001t0005g0240 a0001c0001t0006g0027 a0001c0001t0006g0048 others(4): Show |
8 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.202+2080_202+2081d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | ||||||
| chr11:95801450 | CA | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0101 a0001c0001t0001g0107 others(5): Show |
9 | HG01257.hp1 HG02257.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.202+2081delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95801450 | ||||||
| chr11:95801495 | A | C | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.202+2107A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801495 | |||||||
| chr11:95801763 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0212 a0002c0002t0002g0216 |
4 | HG00099.hp1 HG00639.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+2375G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801763 | |||||||
| chr11:95801829 | A | C | 1 | a0001c0001t0006g0134 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.202+2441A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801829 | |||||||
| chr11:95801924 | A | C | 3 | a0001c0001t0003g0143 a0001c0001t0003g0150 a0001c0001t0003g0151 |
3 | HG02922.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.202+2536A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95801924 | |||||||
| chr11:95802154 | C | T | 1 | a0001c0001t0003g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.202+2766C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802154 | |||||||
| chr11:95802251 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00642.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202+2863C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802251 | |||||||
| chr11:95802255 | A | AT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0110 a0001c0001t0004g0123 others(4): Show |
7 | HG00423.hp1 HG01891.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+2886dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | ||||||
| chr11:95802255 | AT | A | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0003g0155 others(10): Show |
14 | HG02976.hp1 HG03239.hp2 HG03453.hp1 others(11): Show |
intron_variant | MODIFIER | c.202+2886delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | ||||||
| chr11:95802255 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0004g0124 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.202+2876_202+2886d others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95802255 | ||||||
| chr11:95802346 | C | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00642.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.202+2958C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802346 | |||||||
| chr11:95802390 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.202+3002G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802390 | |||||||
| chr11:95802886 | A | C | 2 | a0001c0001t0004g0124 a0001c0001t0004g0126 |
2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.202+3498A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802886 | |||||||
| chr11:95802918 | C | T | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+3530C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802918 | |||||||
| chr11:95802993 | C | A | 3 | a0001c0001t0003g0029 a0001c0001t0003g0156 a0001c0001t0003g0157 |
4 | HG02818.hp1 HG02922.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+3605C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95802993 | |||||||
| chr11:95803047 | A | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG02080.hp2 NA18950.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.202+3659A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803047 | |||||||
| chr11:95803410 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0013g0102 |
2 | HG00280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.202+4022T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803410 | |||||||
| chr11:95803500 | G | T | 1 | a0001c0001t0003g0162 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.202+4112G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803500 | |||||||
| chr11:95803519 | A | G | 1 | a0001c0001t0012g0131 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.202+4131A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803519 | |||||||
| chr11:95803530 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+4142A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803530 | |||||||
| chr11:95803560 | T | C | 97 | a0001c0001t0004g0041 a0001c0001t0005g0039 a0001c0001t0005g0040 others(94): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.202+4172T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803560 | |||||||
| chr11:95803561 | G | GC | 25 | a0001c0001t0001g0108 a0001c0001t0005g0234 a0001c0001t0005g0241 others(22): Show |
28 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.202+4180dupC | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803561 | ||||||
| chr11:95803568 | C | T | 1 | a0001c0001t0003g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.202+4180C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803568 | |||||||
| chr11:95803569 | G | T | 1 | a0001c0001t0007g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.202+4181G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803569 | |||||||
| chr11:95803628 | C | A | 1 | a0002c0002t0002g0189 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.202+4240C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803628 | |||||||
| chr11:95803706 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+4318G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803706 | |||||||
| chr11:95803745 | C | CT | 58 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(55): Show |
70 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.202+4366dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803745 | ||||||
| chr11:95803745 | C | CTT | 16 | a0002c0002t0002g0018 a0002c0002t0002g0185 a0002c0002t0002g0186 others(13): Show |
18 | HG00609.hp1 HG02071.hp1 HG03453.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+4365_202+4366d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95803745 | ||||||
| chr11:95803751 | T | A | 1 | a0001c0003t0005g0250 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202+4363T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95803751 | |||||||
| chr11:95804194 | G | A | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.202+4806G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804194 | |||||||
| chr11:95804352 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0168 |
3 | HG00621.hp2 NA19001.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.202+4964G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804352 | |||||||
| chr11:95804422 | C | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+5034C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804422 | |||||||
| chr11:95804538 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.202+5150C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804538 | |||||||
| chr11:95804575 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.202+5187G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804575 | |||||||
| chr11:95804598 | T | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+5210T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804598 | |||||||
| chr11:95804664 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+5276C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95804664 | |||||||
| chr11:95804721 | TATAA | T | 7 | a0002c0002t0002g0017 a0002c0002t0002g0035 a0002c0002t0002g0174 others(4): Show |
9 | NA18945.hp1 NA18946.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.202+5336_202+5339d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95804721 | ||||||
| chr11:95804867 | A | AT | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.202+5486dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95804867 | ||||||
| chr11:95805106 | G | A | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.202+5718G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805106 | |||||||
| chr11:95805373 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.202+5985C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805373 | |||||||
| chr11:95805378 | T | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202+5990T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805378 | |||||||
| chr11:95805440 | A | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.202+6052A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805440 | |||||||
| chr11:95805459 | C | T | 61 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(58): Show |
100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.202+6071C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805459 | |||||||
| chr11:95805460 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+6072G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805460 | |||||||
| chr11:95805593 | C | A | 1 | a0002c0002t0002g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.202+6205C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805593 | |||||||
| chr11:95805614 | G | A | 61 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(58): Show |
100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.202+6226G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805614 | |||||||
| chr11:95805855 | T | G | 1 | a0002c0002t0002g0224 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.202+6467T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805855 | |||||||
| chr11:95805958 | T | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.202+6570T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95805958 | |||||||
| chr11:95806033 | A | T | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.202+6645A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806033 | |||||||
| chr11:95806110 | A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+6722A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806110 | |||||||
| chr11:95806256 | G | A | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.203-6676G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806256 | |||||||
| chr11:95806353 | G | A | 1 | a0001c0001t0005g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.203-6579G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806353 | |||||||
| chr11:95806354 | G | C | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-6578G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806354 | |||||||
| chr11:95806400 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0101 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.203-6532G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806400 | |||||||
| chr11:95806427 | G | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-6505G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806427 | |||||||
| chr11:95806442 | C | T | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-6490C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806442 | |||||||
| chr11:95806443 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.203-6489G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806443 | |||||||
| chr11:95806450 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.203-6482G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806450 | |||||||
| chr11:95806590 | TG | T | 11 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0140 others(8): Show |
16 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-6341delG | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806590 | |||||||
| chr11:95806611 | G | C | 2 | a0002c0002t0002g0219 a0002c0002t0002g0221 |
2 | HG00639.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.203-6321G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806611 | |||||||
| chr11:95806728 | A | G | 164 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(161): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-6204A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806728 | |||||||
| chr11:95806815 | C | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-6117C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806815 | |||||||
| chr11:95806876 | T | C | 164 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(161): Show |
220 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.203-6056T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806876 | |||||||
| chr11:95806905 | C | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-6027C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806905 | |||||||
| chr11:95806905 | C | T | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-6027C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806905 | |||||||
| chr11:95806998 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-5934C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95806998 | |||||||
| chr11:95807153 | G | T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0242 a0001c0001t0005g0243 |
4 | NA18947.hp1 NA18963.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-5779G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807153 | |||||||
| chr11:95807206 | A | T | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.203-5726A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807206 | |||||||
| chr11:95807212 | A | C | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-5720A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807212 | |||||||
| chr11:95807246 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.203-5686G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807246 | |||||||
| chr11:95807401 | C | T | 61 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(58): Show |
100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.203-5531C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807401 | |||||||
| chr11:95807483 | C | T | 1 | a0002c0002t0002g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.203-5449C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807483 | |||||||
| chr11:95807507 | C | T | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-5425C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807507 | |||||||
| chr11:95807539 | T | C | 1 | a0001c0001t0005g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.203-5393T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807539 | |||||||
| chr11:95807703 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.203-5229G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807703 | |||||||
| chr11:95807763 | G | A | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-5169G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807763 | |||||||
| chr11:95807771 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.203-5161T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95807771 | |||||||
| chr11:95808009 | A | C | 1 | a0002c0002t0002g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.203-4923A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808009 | |||||||
| chr11:95808091 | C | T | 36 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(33): Show |
64 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-4841C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808091 | |||||||
| chr11:95808123 | T | C | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.203-4809T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808123 | |||||||
| chr11:95808308 | A | T | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-4624A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808308 | |||||||
| chr11:95808344 | T | C | 70 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(67): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.203-4588T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808344 | |||||||
| chr11:95808490 | G | C | 1 | a0001c0001t0004g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.203-4442G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808490 | |||||||
| chr11:95808585 | A | G | 61 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(58): Show |
100 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.203-4347A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808585 | |||||||
| chr11:95808783 | T | C | 1 | a0002c0002t0002g0185 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.203-4149T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808783 | |||||||
| chr11:95808850 | G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.203-4082G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808850 | |||||||
| chr11:95808866 | T | C | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-4066T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808866 | |||||||
| chr11:95808932 | A | G | 1 | a0001c0001t0004g0012 | 3 | HG02109.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.203-4000A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95808932 | |||||||
| chr11:95809154 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-3778C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809154 | |||||||
| chr11:95809208 | T | C | 1 | a0001c0001t0005g0247 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.203-3724T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809208 | |||||||
| chr11:95809245 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-3687A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809245 | |||||||
| chr11:95809382 | A | G | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-3550A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809382 | |||||||
| chr11:95809577 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0171 a0001c0001t0001g0172 |
5 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.203-3355C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809577 | |||||||
| chr11:95809581 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-3351A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809581 | |||||||
| chr11:95809684 | G | C | 1 | a0001c0001t0003g0158 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.203-3248G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809684 | |||||||
| chr11:95809692 | A | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.203-3240A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809692 | |||||||
| chr11:95809718 | A | T | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-3214A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809718 | |||||||
| chr11:95809776 | G | T | 1 | a0001c0001t0004g0123 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.203-3156G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95809776 | |||||||
| chr11:95810046 | G | A | 4 | a0002c0002t0002g0186 a0002c0002t0002g0187 a0002c0002t0002g0189 others(1): Show |
4 | HG02071.hp1 NA18942.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.203-2886G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810046 | |||||||
| chr11:95810047 | T | A | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.203-2885T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810047 | |||||||
| chr11:95810355 | A | G | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-2577A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810355 | |||||||
| chr11:95810427 | T | A | 1 | a0002c0002t0002g0222 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.203-2505T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810427 | |||||||
| chr11:95810456 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.203-2476C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810456 | |||||||
| chr11:95810457 | G | A | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-2475G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810457 | |||||||
| chr11:95810470 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.203-2462A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810470 | |||||||
| chr11:95810546 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.203-2386A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810546 | |||||||
| chr11:95810551 | C | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-2381C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810551 | |||||||
| chr11:95810752 | C | T | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-2180C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810752 | |||||||
| chr11:95810816 | C | A | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.203-2116C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810816 | |||||||
| chr11:95810825 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.203-2107G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810825 | |||||||
| chr11:95810851 | A | G | 1 | a0002c0002t0002g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.203-2081A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95810851 | |||||||
| chr11:95811028 | G | A | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.203-1904G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811028 | |||||||
| chr11:95811118 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18939.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.203-1814A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811118 | |||||||
| chr11:95811149 | G | A | 1 | a0002c0002t0002g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.203-1783G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811149 | |||||||
| chr11:95811153 | C | T | 3 | a0001c0001t0008g0235 a0001c0001t0008g0237 a0001c0001t0008g0238 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1779C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811153 | |||||||
| chr11:95811154 | G | T | 3 | a0001c0001t0008g0235 a0001c0001t0008g0237 a0001c0001t0008g0238 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1778G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811154 | |||||||
| chr11:95811155 | G | A | 3 | a0001c0001t0008g0235 a0001c0001t0008g0237 a0001c0001t0008g0238 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.203-1777G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811155 | |||||||
| chr11:95811204 | G | C | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-1728G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811204 | |||||||
| chr11:95811227 | A | G | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.203-1705A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811227 | |||||||
| chr11:95811252 | A | G | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.203-1680A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811252 | |||||||
| chr11:95811428 | C | T | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-1504C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811428 | |||||||
| chr11:95811437 | G | C | 7 | a0002c0002t0002g0038 a0002c0002t0002g0217 a0002c0002t0002g0218 others(4): Show |
8 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.203-1495G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811437 | |||||||
| chr11:95811442 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.203-1490A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811442 | |||||||
| chr11:95811442 | A | T | 1 | a0001c0001t0006g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.203-1490A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811442 | |||||||
| chr11:95811444 | G | C | 1 | a0001c0001t0007g0130 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.203-1488G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811444 | |||||||
| chr11:95811517 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-1415C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811517 | |||||||
| chr11:95811522 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.203-1410A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811522 | |||||||
| chr11:95811580 | T | TA | 6 | a0001c0001t0001g0058 a0001c0001t0005g0245 a0001c0001t0005g0249 others(3): Show |
6 | HG01175.hp2 HG01192.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.203-1338dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811580 | ||||||
| chr11:95811580 | TA | T | 7 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0003g0014 others(4): Show |
9 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.203-1338delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811580 | ||||||
| chr11:95811595 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0094 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.203-1337C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811595 | |||||||
| chr11:95811596 | G | A | 1 | a0002c0002t0002g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.203-1336G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811596 | |||||||
| chr11:95811605 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
4 | HG00621.hp1 NA18939.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.203-1327A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811605 | |||||||
| chr11:95811619 | C | A | 1 | a0001c0001t0004g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.203-1313C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811619 | |||||||
| chr11:95811650 | A | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.203-1282A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811650 | |||||||
| chr11:95811741 | C | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-1191C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811741 | |||||||
| chr11:95811741 | C | T | 1 | a0002c0002t0002g0215 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.203-1191C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811741 | |||||||
| chr11:95811944 | CAT | C | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.203-985_203-984del others(2): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 95811944 | ||||||
| chr11:95811949 | T | G | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.203-983T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95811949 | |||||||
| chr11:95812002 | T | C | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203-930T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812002 | |||||||
| chr11:95812006 | A | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-926A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812006 | |||||||
| chr11:95812020 | G | A | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.203-912G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812020 | |||||||
| chr11:95812069 | A | G | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.203-863A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812069 | |||||||
| chr11:95812160 | T | C | 1 | a0001c0001t0004g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-772T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812160 | |||||||
| chr11:95812176 | T | G | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.203-756T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812176 | |||||||
| chr11:95812205 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.203-727T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812205 | |||||||
| chr11:95812423 | T | A | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.203-509T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812423 | |||||||
| chr11:95812587 | C | T | 1 | a0001c0001t0003g0028 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.203-345C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812587 | |||||||
| chr11:95812791 | C | A | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-141C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812791 | |||||||
| chr11:95812792 | A | C | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.203-140A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 2/10 | chr11 | 95812792 | |||||||
| chr11:95813177 | A | G | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.382+66A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 3/10 | chr11 | 95813177 | |||||||
| chr11:95813628 | T | C | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.504+39T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813628 | |||||||
| chr11:95813763 | T | C | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+174T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813763 | |||||||
| chr11:95813778 | A | G | 2 | a0001c0001t0009g0118 a0001c0001t0009g0122 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.504+189A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813778 | |||||||
| chr11:95813852 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.504+263A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813852 | |||||||
| chr11:95813857 | G | T | 1 | a0002c0002t0002g0203 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.504+268G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813857 | |||||||
| chr11:95813922 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+333G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95813922 | |||||||
| chr11:95814069 | ATCT | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+481_504+483del others(3): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814069 | |||||||
| chr11:95814073 | C | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+484C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814073 | |||||||
| chr11:95814075 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+486C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814075 | |||||||
| chr11:95814076 | T | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+487T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814076 | |||||||
| chr11:95814077 | C | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+488C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814077 | |||||||
| chr11:95814078 | T | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+489T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814078 | |||||||
| chr11:95814166 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.504+577C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814166 | |||||||
| chr11:95814197 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.504+608C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814197 | |||||||
| chr11:95814206 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0009g0118 |
2 | HG02886.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.504+617C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814206 | |||||||
| chr11:95814306 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0163 a0001c0001t0001g0164 others(4): Show |
8 | HG00609.hp2 HG00621.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+717C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814306 | |||||||
| chr11:95814324 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.504+735C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814324 | |||||||
| chr11:95814357 | A | AT | 12 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0067 others(9): Show |
12 | HG00621.hp2 HG02071.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+788dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | ||||||
| chr11:95814357 | A | ATTTT | 15 | a0001c0001t0005g0040 a0001c0001t0005g0233 a0001c0001t0005g0234 others(12): Show |
16 | HG01081.hp2 HG01167.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+785_504+788dup others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | ||||||
| chr11:95814357 | AT | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0079 others(9): Show |
13 | HG02698.hp2 HG02818.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.504+788delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95814357 | ||||||
| chr11:95814403 | C | T | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.504+814C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814403 | |||||||
| chr11:95814422 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.504+833G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814422 | |||||||
| chr11:95814441 | A | G | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.504+852A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814441 | |||||||
| chr11:95814546 | G | C | 1 | a0001c0001t0007g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.504+957G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814546 | |||||||
| chr11:95814651 | C | T | 1 | a0001c0001t0007g0129 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.504+1062C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814651 | |||||||
| chr11:95814670 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.504+1081A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814670 | |||||||
| chr11:95814763 | T | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.504+1174T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814763 | |||||||
| chr11:95814970 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.504+1381T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814970 | |||||||
| chr11:95814985 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.504+1396C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95814985 | |||||||
| chr11:95815136 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0212 a0002c0002t0002g0216 |
4 | HG00099.hp1 HG00639.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1547G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815136 | |||||||
| chr11:95815164 | C | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+1575C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815164 | |||||||
| chr11:95815195 | A | G | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.504+1606A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815195 | |||||||
| chr11:95815404 | C | T | 50 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(47): Show |
84 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.504+1815C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815404 | |||||||
| chr11:95815426 | T | C | 9 | a0001c0001t0004g0023 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
10 | HG02055.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.504+1837T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95815426 | |||||||
| chr11:95815509 | CT | C | 70 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(67): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.504+1929delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 95815509 | ||||||
| chr11:95816503 | T | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02148.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-1284T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816503 | |||||||
| chr11:95816613 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.505-1174C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816613 | |||||||
| chr11:95816784 | G | A | 2 | a0002c0002t0002g0033 a0002c0002t0002g0192 |
3 | HG01168.hp1 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.505-1003G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816784 | |||||||
| chr11:95816823 | C | T | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.505-964C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816823 | |||||||
| chr11:95816923 | A | G | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-864A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95816923 | |||||||
| chr11:95817150 | G | A | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.505-637G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817150 | |||||||
| chr11:95817308 | G | A | 163 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(160): Show |
219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.505-479G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817308 | |||||||
| chr11:95817331 | A | G | 1 | a0001c0001t0005g0233 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.505-456A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817331 | |||||||
| chr11:95817646 | C | G | 36 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(33): Show |
64 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.505-141C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817646 | |||||||
| chr11:95817677 | C | T | 60 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(57): Show |
99 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.505-110C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 4/10 | chr11 | 95817677 | |||||||
| chr11:95817972 | C | T | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.621+69C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95817972 | |||||||
| chr11:95817988 | T | C | 1 | a0002c0002t0002g0182 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.621+85T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95817988 | |||||||
| chr11:95818123 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.621+220T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818123 | |||||||
| chr11:95818133 | C | T | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.621+230C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818133 | |||||||
| chr11:95818276 | G | A | 1 | a0001c0001t0009g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.621+373G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818276 | |||||||
| chr11:95818411 | C | CA | 71 | a0001c0001t0001g0065 a0002c0002t0002g0015 a0002c0002t0002g0016 others(68): Show |
85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.622-401dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 95818411 | ||||||
| chr11:95818430 | A | C | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-397A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818430 | |||||||
| chr11:95818508 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.622-319A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818508 | |||||||
| chr11:95818562 | T | A | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.622-265T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 5/10 | chr11 | 95818562 | |||||||
| chr11:95818948 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.699+44G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95818948 | |||||||
| chr11:95818981 | G | T | 1 | a0001c0001t0003g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.699+77G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95818981 | |||||||
| chr11:95819001 | T | G | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.699+97T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819001 | |||||||
| chr11:95819145 | C | A | 3 | a0002c0002t0002g0036 a0002c0002t0002g0190 a0002c0002t0002g0211 |
4 | NA18968.hp1 NA18970.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+241C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819145 | |||||||
| chr11:95819596 | A | C | 1 | a0001c0001t0006g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.699+692A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819596 | |||||||
| chr11:95819739 | C | T | 22 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.699+835C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819739 | |||||||
| chr11:95819872 | C | G | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.699+968C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95819872 | |||||||
| chr11:95819904 | T | TTTG | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.699+1009_699+1011d others(5): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95819904 | ||||||
| chr11:95820351 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.699+1447G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820351 | |||||||
| chr11:95820360 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.699+1456T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820360 | |||||||
| chr11:95820367 | CTGAGGTC others(7): Show |
C | 2 | a0001c0001t0003g0030 a0001c0001t0003g0142 |
3 | NA18943.hp1 NA19054.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.699+1482_700-1472d others(16): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820367 | ||||||
| chr11:95820464 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.700-1407G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820464 | |||||||
| chr11:95820538 | T | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0199 |
2 | NA18954.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.700-1333T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820538 | |||||||
| chr11:95820579 | C | CA | 31 | a0001c0001t0001g0062 a0001c0001t0001g0085 a0001c0001t0001g0096 others(28): Show |
33 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.700-1274dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | ||||||
| chr11:95820579 | C | CAAAA | 55 | a0002c0002t0002g0016 a0002c0002t0002g0017 a0002c0002t0002g0018 others(52): Show |
66 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.700-1277_700-1274d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | ||||||
| chr11:95820579 | C | CAAAAA | 17 | a0002c0002t0002g0015 a0002c0002t0002g0033 a0002c0002t0002g0042 others(14): Show |
20 | HG00438.hp1 HG01071.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.700-1278_700-1274d others(7): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 95820579 | ||||||
| chr11:95820726 | G | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-1145G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820726 | |||||||
| chr11:95820802 | T | C | 2 | a0002c0002t0002g0184 a0002c0002t0002g0196 |
2 | HG02135.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.700-1069T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95820802 | |||||||
| chr11:95821006 | A | G | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-865A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821006 | |||||||
| chr11:95821119 | G | A | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.700-752G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821119 | |||||||
| chr11:95821147 | A | G | 70 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(67): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.700-724A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821147 | |||||||
| chr11:95821427 | A | G | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.700-444A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821427 | |||||||
| chr11:95821752 | A | G | 1 | a0001c0001t0005g0239 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-119A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821752 | |||||||
| chr11:95821777 | A | G | 1 | a0002c0002t0002g0208 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.700-94A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 6/10 | chr11 | 95821777 | |||||||
| chr11:95821986 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | NA18950.hp1 NA18970.hp2 NA19062.hp1 |
splice_region_variant&intron_variant | LOW | c.807+8G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/10 | chr11 | 95821986 | |||||||
| chr11:95822380 | A | C | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.808-119A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 7/10 | chr11 | 95822380 | |||||||
| chr11:95822677 | G | GTGCCTTT others(16): Show |
74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.885+102_885+124dup others(23): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95822677 | ||||||
| chr11:95823017 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0128 |
2 | HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.885+441C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823017 | |||||||
| chr11:95823018 | G | A | 33 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(30): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.885+442G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823018 | |||||||
| chr11:95823093 | G | A | 25 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(22): Show |
27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.885+517G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823093 | |||||||
| chr11:95823139 | G | T | 1 | a0002c0002t0002g0195 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.885+563G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823139 | |||||||
| chr11:95823400 | T | C | 3 | a0001c0001t0008g0235 a0001c0001t0008g0237 a0001c0001t0008g0238 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.885+824T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823400 | |||||||
| chr11:95823532 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.885+956C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823532 | |||||||
| chr11:95823552 | GT | G | 19 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(16): Show |
25 | HG00323.hp2 HG02300.hp2 HG02630.hp1 others(22): Show |
intron_variant | MODIFIER | c.885+984delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823552 | ||||||
| chr11:95823570 | T | G | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.885+994T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823570 | |||||||
| chr11:95823592 | GACT | G | 6 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0144 others(3): Show |
12 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.885+1019_885+1021d others(5): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823592 | ||||||
| chr11:95823630 | CAG | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.885+1058_885+1059d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823630 | ||||||
| chr11:95823691 | C | T | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.885+1115C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823691 | |||||||
| chr11:95823784 | T | G | 1 | a0002c0002t0002g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.885+1208T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823784 | |||||||
| chr11:95823838 | C | A | 1 | a0001c0001t0003g0156 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.885+1262C>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95823838 | |||||||
| chr11:95823865 | G | GTTTA | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.885+1290_885+1293d others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95823865 | ||||||
| chr11:95824070 | T | C | 1 | a0002c0002t0002g0207 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.885+1494T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824070 | |||||||
| chr11:95824073 | T | TA | 22 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(19): Show |
27 | HG02055.hp1 HG02135.hp1 HG02559.hp1 others(24): Show |
intron_variant | MODIFIER | c.885+1520dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | ||||||
| chr11:95824073 | TA | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0001c0001t0003g0161 others(84): Show |
101 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.885+1520delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | ||||||
| chr11:95824073 | TAA | T | 8 | a0001c0001t0005g0241 a0001c0003t0005g0252 a0002c0002t0002g0032 others(5): Show |
9 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1519_885+1520d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824073 | ||||||
| chr11:95824258 | T | A | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+1682T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824258 | |||||||
| chr11:95824259 | A | T | 49 | a0001c0001t0001g0063 a0001c0001t0003g0001 a0001c0001t0003g0005 others(46): Show |
83 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.885+1683A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824259 | |||||||
| chr11:95824260 | A | T | 4 | a0001c0001t0004g0023 a0001c0001t0004g0041 a0001c0001t0004g0115 others(1): Show |
5 | HG02257.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+1684A>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824260 | |||||||
| chr11:95824351 | G | A | 5 | a0001c0001t0005g0039 a0001c0001t0005g0240 a0001c0001t0005g0244 others(2): Show |
6 | NA18940.hp1 NA18945.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.885+1775G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824351 | |||||||
| chr11:95824406 | ACT | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.885+1833_885+1834d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95824406 | ||||||
| chr11:95824552 | G | A | 1 | a0002c0002t0004g0232 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.885+1976G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824552 | |||||||
| chr11:95824874 | C | G | 1 | a0002c0002t0002g0205 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.885+2298C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824874 | |||||||
| chr11:95824983 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.885+2407C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95824983 | |||||||
| chr11:95825100 | C | T | 2 | a0001c0001t0003g0153 a0001c0001t0003g0160 |
2 | HG00423.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.885+2524C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825100 | |||||||
| chr11:95825254 | T | A | 25 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(22): Show |
27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.886-2532T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825254 | |||||||
| chr11:95825395 | C | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2391C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825395 | |||||||
| chr11:95825411 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.886-2375G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825411 | |||||||
| chr11:95825454 | A | G | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.886-2332A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825454 | |||||||
| chr11:95825593 | C | CT | 18 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0077 others(15): Show |
20 | HG01175.hp2 HG02055.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.886-2172dupT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | ||||||
| chr11:95825593 | C | CTT | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-2173_886-2172d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | ||||||
| chr11:95825593 | CT | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(17): Show |
25 | HG00438.hp1 HG01168.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.886-2172delT | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825593 | ||||||
| chr11:95825611 | T | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.886-2175T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825611 | |||||||
| chr11:95825631 | C | G | 1 | a0002c0002t0002g0212 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.886-2155C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825631 | |||||||
| chr11:95825782 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.886-2004A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825782 | |||||||
| chr11:95825789 | G | T | 1 | a0002c0002t0002g0229 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.886-1997G>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95825789 | |||||||
| chr11:95825871 | TCTGTAAT others(4): Show |
T | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.886-1903_886-1893d others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95825871 | ||||||
| chr11:95826033 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.886-1753G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826033 | |||||||
| chr11:95826074 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0083 |
3 | HG01496.hp2 HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.886-1712A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826074 | |||||||
| chr11:95826105 | T | C | 1 | a0001c0001t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.886-1681T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826105 | |||||||
| chr11:95826106 | T | A | 1 | a0001c0001t0003g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.886-1680T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826106 | |||||||
| chr11:95826165 | C | T | 6 | a0001c0001t0006g0027 a0001c0001t0006g0048 a0001c0001t0006g0132 others(3): Show |
7 | HG03239.hp2 HG03491.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.886-1621C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826165 | |||||||
| chr11:95826223 | T | C | 1 | a0001c0001t0005g0244 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.886-1563T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826223 | |||||||
| chr11:95826353 | T | C | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.886-1433T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826353 | |||||||
| chr11:95826600 | GA | G | 47 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(44): Show |
81 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.886-1177delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 95826600 | ||||||
| chr11:95826645 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.886-1141C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826645 | |||||||
| chr11:95826677 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.886-1109C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826677 | |||||||
| chr11:95826745 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(8): Show |
16 | HG02300.hp2 HG02630.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.886-1041T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826745 | |||||||
| chr11:95826825 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | NA18939.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.886-961T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826825 | |||||||
| chr11:95826930 | A | G | 4 | a0001c0001t0003g0014 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
6 | HG02258.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.886-856A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95826930 | |||||||
| chr11:95827083 | T | G | 1 | a0001c0001t0003g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.886-703T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827083 | |||||||
| chr11:95827207 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.886-579G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827207 | |||||||
| chr11:95827221 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.886-565A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827221 | |||||||
| chr11:95827284 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.886-502C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827284 | |||||||
| chr11:95827309 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.886-477T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827309 | |||||||
| chr11:95827375 | T | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.886-411T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827375 | |||||||
| chr11:95827531 | A | G | 50 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0007 others(47): Show |
84 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.886-255A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827531 | |||||||
| chr11:95827590 | TTTTCCAT others(6): Show |
T | 13 | a0001c0001t0004g0006 a0001c0001t0004g0012 a0001c0001t0004g0023 others(10): Show |
19 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.886-195_886-183del others(13): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827590 | |||||||
| chr11:95827684 | A | C | 1 | a0001c0001t0004g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.886-102A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827684 | |||||||
| chr11:95827689 | A | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.886-97A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 8/10 | chr11 | 95827689 | |||||||
| chr11:95828028 | G | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | splice_donor_variant&intron_variant | HIGH | c.1127+1G>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828028 | |||||||
| chr11:95828041 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+14T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828041 | |||||||
| chr11:95828042 | T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+15T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828042 | |||||||
| chr11:95828046 | T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+19T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828046 | |||||||
| chr11:95828047 | T | A | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+20T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828047 | |||||||
| chr11:95828049 | T | A | 1 | a0001c0001t0001g0013 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1127+22T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828049 | |||||||
| chr11:95828051 | A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+24A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828051 | |||||||
| chr11:95828054 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+27T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828054 | |||||||
| chr11:95828058 | T | A | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+31T>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828058 | |||||||
| chr11:95828059 | T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+32T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828059 | |||||||
| chr11:95828064 | T | TCGAAACA others(4): Show |
1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+38_1127+39ins others(11): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828064 | ||||||
| chr11:95828069 | A | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+42A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828069 | |||||||
| chr11:95828072 | C | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+45C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828072 | |||||||
| chr11:95828073 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+46T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828073 | |||||||
| chr11:95828077 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+50T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828077 | |||||||
| chr11:95828078 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+51T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828078 | |||||||
| chr11:95828079 | T | C | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+52T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828079 | |||||||
| chr11:95828085 | A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+58A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828085 | |||||||
| chr11:95828086 | A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+59A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828086 | |||||||
| chr11:95828092 | T | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+65T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828092 | |||||||
| chr11:95828101 | TA | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1127+77delA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828101 | ||||||
| chr11:95828130 | A | G | 25 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 others(22): Show |
27 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1127+103A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828130 | |||||||
| chr11:95828149 | A | G | 1 | a0004c0009t0001g0088 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1127+122A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828149 | |||||||
| chr11:95828324 | T | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1127+297T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828324 | |||||||
| chr11:95828480 | C | CAT | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1127+454_1127+455d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95828480 | ||||||
| chr11:95828505 | A | G | 1 | a0002c0002t0002g0210 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1127+478A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828505 | |||||||
| chr11:95828518 | G | A | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1127+491G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828518 | |||||||
| chr11:95828553 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1127+526A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828553 | |||||||
| chr11:95828577 | C | T | 96 | a0001c0001t0005g0039 a0001c0001t0005g0040 a0001c0001t0005g0233 others(93): Show |
112 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1127+550C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828577 | |||||||
| chr11:95828709 | C | T | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1128-478C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828709 | |||||||
| chr11:95828801 | A | G | 1 | a0001c0001t0004g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1128-386A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828801 | |||||||
| chr11:95828959 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1128-228G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95828959 | |||||||
| chr11:95829041 | C | CA | 16 | a0001c0001t0001g0172 a0001c0001t0004g0006 a0001c0001t0004g0012 others(13): Show |
22 | HG01109.hp2 HG01123.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1128-130dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 95829041 | ||||||
| chr11:95829107 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1128-80G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95829107 | |||||||
| chr11:95829163 | G | A | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1128-24G>A | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 9/10 | chr11 | 95829163 | |||||||
| chr11:95829371 | G | GA | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1272+50dupA | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 95829371 | ||||||
| chr11:95829381 | A | C | 1 | a0001c0001t0011g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1272+50A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829381 | |||||||
| chr11:95829607 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1272+276T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829607 | |||||||
| chr11:95829666 | TAA | T | 3 | a0001c0001t0004g0124 a0001c0001t0004g0125 a0001c0001t0004g0126 |
3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1272+336_1272+337d others(4): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829666 | |||||||
| chr11:95829704 | C | G | 73 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(70): Show |
87 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1272+373C>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829704 | |||||||
| chr11:95829835 | A | G | 22 | a0001c0001t0003g0001 a0001c0001t0003g0028 a0001c0001t0003g0029 others(19): Show |
41 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.1272+504A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95829835 | |||||||
| chr11:95830064 | T | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1272+733T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830064 | |||||||
| chr11:95830202 | A | C | 2 | a0001c0001t0003g0150 a0001c0001t0003g0151 |
2 | HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1273-824A>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830202 | |||||||
| chr11:95830318 | T | C | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1273-708T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830318 | |||||||
| chr11:95830342 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1273-684A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830342 | |||||||
| chr11:95830434 | C | T | 1 | a0001c0001t0004g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1273-592C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830434 | |||||||
| chr11:95830566 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0046 |
6 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273-460C>T | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830566 | |||||||
| chr11:95830581 | T | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0080 others(1): Show |
9 | NA18942.hp2 NA18956.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273-445T>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830581 | |||||||
| chr11:95830611 | A | G | 74 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0017 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1273-415A>G | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830611 | |||||||
| chr11:95830885 | T | C | 1 | a0001c0001t0007g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1273-141T>C | CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | chr11 | 95830885 | |||||||
| chr11:95830910 | T | TTGAG | 154 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0026 others(151): Show |
201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1273-115_1273-114i others(6): Show |
CEP57 | ENSG00000166037.11 | transcript | ENST00000325542.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 95830910 |