Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79959 |
| ensemblid | ENSG00000101624.11 |
| hgncid | 25727 |
| symbol | CEP76 |
| name | centrosomal protein 76 |
| refseq_nuc | NM_024899.4 |
| refseq_prot | NP_079175.2 |
| ensembl_nuc | ENST00000262127.7 |
| ensembl_prot | ENSP00000262127.2 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 12672625 |
| end | 12702723 |
| strand | - |
| ver | v1.2 |
| region | chr18:12672625-12702723 |
| region5000 | chr18:12667625-12707723 |
| regionname0 | CEP76_chr18_12672625_12702723 |
| regionname5000 | CEP76_chr18_12667625_12707723 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 659 | 365 | 88 | 67 | 154 | 12 | 42 | 121 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| a0002 | 0/0 | 659 | 11 | 0 | 3 | 8 | 0 | 0 | 7 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| a0003 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| a0004 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| a0005 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| a0006 | 0/0 | 659 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | MSLPP others(654): Show |
chr18 | 12667625 | 12707723 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1977 | 365 | 88 | 67 | 154 | 12 | 42 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 | ||
| a0002c0002 | 0/0 | 1977 | 11 | 0 | 3 | 8 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 | ||
| a0003c0006 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 | ||
| a0004c0004 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 | ||
| a0005c0003 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 | ||
| a0006c0005 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATGTC others(1972): Show |
chr18 | 12667625 | 12707723 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2895 | 271 | 63 | 50 | 112 | 9 | 36 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0002 | 0/0 | 2895 | 59 | 3 | 10 | 42 | 1 | 3 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0003 | 0/1 | 2895 | 19 | 12 | 3 | 0 | 1 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0004 | 0/0 | 2895 | 6 | 3 | 2 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0005 | 0/0 | 2895 | 6 | 6 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0006 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0007 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0008 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0001c0001t0009 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0002c0002t0001 | 0/0 | 2895 | 11 | 0 | 3 | 8 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0003c0006t0001 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0004c0004t0001 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0005c0003t0001 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| a0006c0005t0001 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | ATTTC others(2890): Show |
chr18 | 12667625 | 12707723 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 0 | 8 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0002 | 0/0 | 8 | 2 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0037 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0005 | 0/0 | 7 | 1 | 2 | 4 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0006 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0003c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0004c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0005c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| a0006c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0115 | EUR | FIN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0060 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02965 | hp1 | a0003 | c0006 | t0001 | g0055 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03486 | hp1 | a0004 | c0004 | t0001 | g0188 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0257 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18975 | hp2 | a0005 | c0003 | t0001 | g0083 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19011 | hp2 | a0006 | c0005 | t0001 | g0138 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ASW | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ASW | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0184 | EUR | TSI | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0111 | REF | REF | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0037 | REF | REF | CEP76_chr18_12667625_12707723 | CEP76 | chr18 | 12667625 | 12707723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12674674 | C | T | 1 | a0006 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1703G>A | p.Arg568His | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/12 | 1878/2895 | 1703/1980 | 568/659 | chr18 | 12674674 | |||
| chr18:12686401 | C | T | 1 | a0005 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.983G>A | p.Arg328Gln | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/12 | 1158/2895 | 983/1980 | 328/659 | chr18 | 12686401 | |||
| chr18:12697231 | A | G | 1 | a0004 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.698T>C | p.Met233Thr | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/12 | 873/2895 | 698/1980 | 233/659 | chr18 | 12697231 | |||
| chr18:12697355 | T | C | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.574A>G | p.Ile192Val | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/12 | 749/2895 | 574/1980 | 192/659 | chr18 | 12697355 | |||
| chr18:12698984 | C | T | 2 | a0002 a0005 |
12 | HG01192.hp1 HG01257.hp1 HG02004.hp1 others(9): Show |
missense_variant | MODERATE | c.515G>A | p.Ser172Asn | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/12 | 690/2895 | 515/1980 | 172/659 | chr18 | 12698984 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12672656 | A | G | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 709 | chr18 | 12672656 | ||||||
| chr18:12672934 | G | A | 1 | a0001c0001t0009 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 431 | chr18 | 12672934 | ||||||
| chr18:12672957 | A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*408T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 408 | chr18 | 12672957 | ||||||
| chr18:12673137 | C | G | 1 | a0001c0001t0005 | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 228 | chr18 | 12673137 | ||||||
| chr18:12673188 | T | C | 2 | a0001c0001t0005 a0001c0001t0008 |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*177A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 177 | chr18 | 12673188 | ||||||
| chr18:12673196 | G | A | 1 | a0001c0001t0004 | 6 | HG01243.hp2 HG01256.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*169C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 169 | chr18 | 12673196 | ||||||
| chr18:12673232 | T | G | 1 | a0001c0001t0005 | 6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*133A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 12/12 | 133 | chr18 | 12673232 | ||||||
| chr18:12702594 | C | T | 1 | a0001c0001t0006 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-46G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | 46 | chr18 | 12702594 | ||||||
| chr18:12702611 | G | A | 2 | a0001c0001t0001 a0001c0001t0006 |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | chr18 | 12702611 | |||||||
| chr18:12702706 | G | C | 2 | a0001c0001t0002 a0001c0001t0009 |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-158C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/12 | 158 | chr18 | 12702706 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:12673532 | TAAG | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0226 |
4 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842-32_1842-30del others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673532 | |||||||
| chr18:12673540 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1842-37C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673540 | |||||||
| chr18:12673575 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1842-72G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673575 | |||||||
| chr18:12673708 | C | T | 3 | a0001c0001t0003g0010 a0001c0001t0003g0179 a0001c0001t0003g0180 |
6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842-205G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673708 | |||||||
| chr18:12673722 | A | G | 51 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(48): Show |
71 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1842-219T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673722 | |||||||
| chr18:12673807 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1842-304C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673807 | |||||||
| chr18:12673849 | A | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1842-346T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673849 | |||||||
| chr18:12673868 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1842-365C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12673868 | |||||||
| chr18:12674422 | G | T | 1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1841+114C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674422 | |||||||
| chr18:12674441 | T | TA | 6 | a0001c0001t0001g0139 a0001c0001t0001g0146 a0001c0001t0001g0155 others(3): Show |
6 | HG01928.hp2 HG03710.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.1841+94dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674441 | |||||||
| chr18:12674441 | TA | T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
34 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1841+94delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 11/11 | chr18 | 12674441 | |||||||
| chr18:12674778 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1624-25T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674778 | |||||||
| chr18:12674852 | G | T | 10 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0212 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1624-99C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674852 | |||||||
| chr18:12674965 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0226 |
4 | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-212G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12674965 | |||||||
| chr18:12675077 | T | TACATTTT others(3): Show |
6 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-325_1624-324i others(12): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675077 | |||||||
| chr18:12675077 | T | TATATTTT others(3): Show |
65 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(62): Show |
89 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1624-334_1624-325d others(12): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675077 | |||||||
| chr18:12675159 | G | C | 2 | a0001c0001t0005g0049 a0001c0001t0005g0060 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1624-406C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675159 | |||||||
| chr18:12675318 | T | C | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1624-565A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675318 | |||||||
| chr18:12675345 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1624-592C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675345 | |||||||
| chr18:12675568 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0140 |
2 | HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1624-815A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675568 | |||||||
| chr18:12675680 | AT | A | 6 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-928delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675680 | |||||||
| chr18:12675700 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1624-947T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675700 | |||||||
| chr18:12675904 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1624-1151T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675904 | |||||||
| chr18:12675924 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1624-1171G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675924 | |||||||
| chr18:12675937 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1624-1184C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675937 | |||||||
| chr18:12675958 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1624-1205G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12675958 | |||||||
| chr18:12676010 | G | A | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1624-1257C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676010 | |||||||
| chr18:12676174 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1624-1421G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676174 | |||||||
| chr18:12676175 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1422C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676175 | |||||||
| chr18:12676279 | C | CT | 75 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0027 others(72): Show |
103 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1624-1527dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676279 | |||||||
| chr18:12676279 | C | CTT | 5 | a0001c0001t0001g0214 a0001c0001t0001g0221 a0001c0001t0002g0044 others(2): Show |
6 | HG03688.hp1 NA18944.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1624-1528_1624-152 others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676279 | |||||||
| chr18:12676350 | C | G | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1624-1597G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676350 | |||||||
| chr18:12676459 | G | GAGAT | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(63): Show |
96 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1623+1646_1623+164 others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676459 | |||||||
| chr18:12676476 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1623+1633G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676476 | |||||||
| chr18:12676765 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1623+1344C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676765 | |||||||
| chr18:12676773 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1623+1336T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676773 | |||||||
| chr18:12676786 | A | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0127 others(2): Show |
6 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+1323T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12676786 | |||||||
| chr18:12677033 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1623+1076T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677033 | |||||||
| chr18:12677045 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1623+1064G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677045 | |||||||
| chr18:12677184 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1623+925C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677184 | |||||||
| chr18:12677237 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0136 a0001c0001t0001g0150 |
4 | HG01081.hp2 HG01261.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+872G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677237 | |||||||
| chr18:12677299 | G | A | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1623+810C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677299 | |||||||
| chr18:12677394 | C | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01952.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1623+715G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677394 | |||||||
| chr18:12677422 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0207 a0001c0001t0001g0222 |
4 | HG00558.hp1 HG00597.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+687C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677422 | |||||||
| chr18:12677458 | C | CA | 26 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0048 others(23): Show |
29 | HG00621.hp1 HG00621.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1623+650dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | |||||||
| chr18:12677458 | CA | C | 35 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(32): Show |
45 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1623+650delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | |||||||
| chr18:12677458 | CAA | C | 52 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(49): Show |
71 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1623+649_1623+650d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677458 | |||||||
| chr18:12677696 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1623+413G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677696 | |||||||
| chr18:12677740 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1623+369A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677740 | |||||||
| chr18:12677935 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1623+174C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12677935 | |||||||
| chr18:12678031 | C | T | 2 | a0001c0001t0001g0050 a0003c0006t0001g0055 |
2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1623+78G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 10/11 | chr18 | 12678031 | |||||||
| chr18:12678487 | A | G | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1290-45T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678487 | |||||||
| chr18:12678697 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290-255C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678697 | |||||||
| chr18:12678699 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1290-257A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678699 | |||||||
| chr18:12678722 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1290-280C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678722 | |||||||
| chr18:12678726 | CA | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0189 a0004c0004t0001g0188 |
5 | HG01884.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1290-285delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678726 | |||||||
| chr18:12678729 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1290-287C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678729 | |||||||
| chr18:12678784 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290-342G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678784 | |||||||
| chr18:12678842 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290-400C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678842 | |||||||
| chr18:12678926 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1290-484G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678926 | |||||||
| chr18:12678950 | A | G | 20 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0065 others(17): Show |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1290-508T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12678950 | |||||||
| chr18:12679093 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1290-651C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679093 | |||||||
| chr18:12679326 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1290-884T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679326 | |||||||
| chr18:12679388 | G | GAGGCAGG others(12): Show |
1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1290-965_1290-947d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679388 | |||||||
| chr18:12679401 | C | T | 1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1290-959G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679401 | |||||||
| chr18:12679413 | G | GGAAGCAC others(12): Show |
1 | a0001c0001t0004g0178 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1290-990_1290-972d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679413 | |||||||
| chr18:12679413 | GGAAGCAC others(12): Show |
G | 1 | a0001c0001t0001g0224 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1290-990_1290-972d others(21): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679413 | |||||||
| chr18:12679760 | C | G | 2 | a0001c0001t0005g0049 a0001c0001t0005g0060 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1289+902G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679760 | |||||||
| chr18:12679829 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1289+833C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679829 | |||||||
| chr18:12679864 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1289+798T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12679864 | |||||||
| chr18:12680052 | C | CA | 8 | a0001c0001t0001g0038 a0001c0001t0002g0270 a0001c0001t0003g0112 others(5): Show |
9 | HG00280.hp2 HG01192.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1289+609dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680052 | |||||||
| chr18:12680084 | AT | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
6 | NA18946.hp2 NA18950.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1289+577delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680084 | |||||||
| chr18:12680274 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1289+388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680274 | |||||||
| chr18:12680519 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1289+143G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680519 | |||||||
| chr18:12680522 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1289+140C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680522 | |||||||
| chr18:12680562 | A | G | 1 | a0002c0002t0001g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1289+100T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680562 | |||||||
| chr18:12680596 | C | CA | 5 | a0001c0001t0001g0038 a0001c0001t0001g0205 a0001c0001t0001g0215 others(2): Show |
6 | HG00738.hp1 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1289+65dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | |||||||
| chr18:12680596 | CA | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(154): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1289+65delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | |||||||
| chr18:12680596 | CAA | C | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
29 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1289+64_1289+65del others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 9/11 | chr18 | 12680596 | |||||||
| chr18:12680969 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1123-141G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12680969 | |||||||
| chr18:12681130 | G | A | 1 | a0001c0001t0005g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1123-302C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681130 | |||||||
| chr18:12681198 | C | CA | 31 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
34 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.1123-371dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681198 | |||||||
| chr18:12681255 | CA | C | 1 | a0001c0001t0001g0014 | 3 | HG01884.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1123-428delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681255 | |||||||
| chr18:12681256 | A | AT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0018 others(32): Show |
40 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1123-429dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | |||||||
| chr18:12681256 | A | ATT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(18): Show |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1123-430_1123-429d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | |||||||
| chr18:12681256 | A | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(4): Show |
8 | HG00673.hp1 HG02027.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.1123-428T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | |||||||
| chr18:12681256 | AT | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0052 others(18): Show |
23 | HG00408.hp1 HG01243.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1123-429delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | |||||||
| chr18:12681256 | ATT | A | 38 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(35): Show |
56 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1123-430_1123-429d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681256 | |||||||
| chr18:12681437 | CAG | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1123-611_1123-610d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681437 | |||||||
| chr18:12681691 | A | G | 20 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0065 others(17): Show |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1123-863T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681691 | |||||||
| chr18:12681711 | GAAC | G | 5 | a0001c0001t0005g0049 a0001c0001t0005g0057 a0001c0001t0005g0058 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1123-886_1123-884d others(5): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681711 | |||||||
| chr18:12681947 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1119C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681947 | |||||||
| chr18:12681996 | T | TA | 7 | a0001c0001t0001g0146 a0001c0001t0005g0049 a0001c0001t0005g0056 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-1169dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12681996 | |||||||
| chr18:12682135 | G | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-1307C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682135 | |||||||
| chr18:12682171 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1123-1343A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682171 | |||||||
| chr18:12682214 | G | A | 20 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0065 others(17): Show |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1123-1386C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682214 | |||||||
| chr18:12682698 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1123-1870C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682698 | |||||||
| chr18:12682936 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1123-2108C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682936 | |||||||
| chr18:12682970 | A | T | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1123-2142T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12682970 | |||||||
| chr18:12683116 | C | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1123-2288G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683116 | |||||||
| chr18:12683119 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1123-2291C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683119 | |||||||
| chr18:12683186 | C | CA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0047 others(25): Show |
33 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1123-2359dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAA | 7 | a0001c0001t0001g0208 a0001c0001t0005g0049 a0001c0001t0005g0056 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1123-2360_1123-235 others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
11 | HG00280.hp1 HG00735.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123-2364_1123-235 others(10): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1123-2370_1123-235 others(16): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(6): Show |
22 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0002g0004 others(19): Show |
33 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1123-2371_1123-235 others(17): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(7): Show |
23 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0054 others(20): Show |
33 | HG00544.hp1 HG00673.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1123-2372_1123-235 others(18): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0053 a0001c0001t0002g0269 |
2 | HG03579.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1123-2373_1123-235 others(19): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1123-2374_1123-235 others(20): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1123-2376_1123-235 others(22): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(13): Show |
1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1123-2359_1123-235 others(24): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683186 | C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1123-2359_1123-235 others(27): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683186 | |||||||
| chr18:12683345 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1123-2517G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683345 | |||||||
| chr18:12683469 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1123-2641T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683469 | |||||||
| chr18:12683550 | A | C | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1122+2712T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683550 | |||||||
| chr18:12683567 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1122+2695T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683567 | |||||||
| chr18:12683640 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1122+2622T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683640 | |||||||
| chr18:12683806 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1122+2456T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683806 | |||||||
| chr18:12683991 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1122+2271T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683991 | |||||||
| chr18:12683999 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+2263A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12683999 | |||||||
| chr18:12684033 | A | C | 1 | a0001c0001t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2229T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684033 | |||||||
| chr18:12684045 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2217C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684045 | |||||||
| chr18:12684049 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1122+2213C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684049 | |||||||
| chr18:12684063 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1122+2199G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684063 | |||||||
| chr18:12684064 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1122+2198C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684064 | |||||||
| chr18:12684088 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122+2174C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684088 | |||||||
| chr18:12684088 | G | T | 1 | a0001c0001t0007g0114 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1122+2174C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684088 | |||||||
| chr18:12684097 | T | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+2165A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684097 | |||||||
| chr18:12684171 | G | A | 1 | a0001c0001t0004g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1122+2091C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684171 | |||||||
| chr18:12684180 | A | T | 1 | a0001c0001t0002g0253 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1122+2082T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684180 | |||||||
| chr18:12684202 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1122+2060G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684202 | |||||||
| chr18:12684282 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1122+1980A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684282 | |||||||
| chr18:12684335 | G | C | 6 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122+1927C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684335 | |||||||
| chr18:12684421 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+1841G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684421 | |||||||
| chr18:12684460 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1122+1802A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684460 | |||||||
| chr18:12684485 | GT | G | 70 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(67): Show |
94 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1122+1776delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684485 | |||||||
| chr18:12684492 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1122+1770A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684492 | |||||||
| chr18:12684536 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1122+1726C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684536 | |||||||
| chr18:12684697 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1122+1565C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684697 | |||||||
| chr18:12684700 | C | G | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+1562G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684700 | |||||||
| chr18:12684925 | C | A | 18 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.1122+1337G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12684925 | |||||||
| chr18:12685005 | A | T | 1 | a0001c0001t0006g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1122+1257T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685005 | |||||||
| chr18:12685113 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1122+1149C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685113 | |||||||
| chr18:12685202 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0124 |
3 | HG02698.hp2 HG03490.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1122+1060C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685202 | |||||||
| chr18:12685322 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1122+940C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685322 | |||||||
| chr18:12685346 | C | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(57): Show |
88 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1122+916G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685346 | |||||||
| chr18:12685396 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1122+866G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685396 | |||||||
| chr18:12685405 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122+857T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685405 | |||||||
| chr18:12685575 | G | A | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1122+687C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685575 | |||||||
| chr18:12685607 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1122+655G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685607 | |||||||
| chr18:12685637 | AT | A | 66 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(63): Show |
90 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1122+624delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685637 | |||||||
| chr18:12685638 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1122+624A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685638 | |||||||
| chr18:12685639 | T | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1122+623A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685639 | |||||||
| chr18:12685658 | T | A | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1122+604A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685658 | |||||||
| chr18:12685695 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+567C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685695 | |||||||
| chr18:12685717 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1122+545G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685717 | |||||||
| chr18:12685751 | C | T | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1122+511G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685751 | |||||||
| chr18:12685900 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1122+362C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685900 | |||||||
| chr18:12685904 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1122+358A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685904 | |||||||
| chr18:12685974 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1122+288T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685974 | |||||||
| chr18:12685984 | A | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1122+278T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12685984 | |||||||
| chr18:12686029 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122+233T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686029 | |||||||
| chr18:12686050 | A | G | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122+212T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686050 | |||||||
| chr18:12686063 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1122+199A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686063 | |||||||
| chr18:12686091 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1122+171G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686091 | |||||||
| chr18:12686247 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122+15T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 8/11 | chr18 | 12686247 | |||||||
| chr18:12686464 | G | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-14C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686464 | |||||||
| chr18:12686674 | G | A | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.934-224C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686674 | |||||||
| chr18:12686764 | G | C | 38 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(35): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.934-314C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12686764 | |||||||
| chr18:12687028 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.934-578C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687028 | |||||||
| chr18:12687139 | C | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-689G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687139 | |||||||
| chr18:12687254 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-804A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687254 | |||||||
| chr18:12687414 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.934-964A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687414 | |||||||
| chr18:12687454 | A | AT | 13 | a0001c0001t0001g0061 a0001c0001t0001g0092 a0001c0001t0001g0104 others(10): Show |
13 | HG00438.hp2 HG01109.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.934-1005dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687454 | |||||||
| chr18:12687454 | AT | A | 18 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0051 others(15): Show |
20 | HG00140.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.934-1005delA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687454 | |||||||
| chr18:12687474 | G | T | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.934-1024C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687474 | |||||||
| chr18:12687669 | T | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0234 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.934-1219A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687669 | |||||||
| chr18:12687693 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.934-1243A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687693 | |||||||
| chr18:12687713 | A | G | 6 | a0001c0001t0001g0107 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | NA18948.hp2 NA18955.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1263T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687713 | |||||||
| chr18:12687773 | AAC | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.934-1325_934-1324d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687773 | |||||||
| chr18:12687906 | G | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1456C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687906 | |||||||
| chr18:12687926 | T | G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.934-1476A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687926 | |||||||
| chr18:12687970 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0003g0112 others(1): Show |
4 | HG02738.hp2 HG03239.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-1520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12687970 | |||||||
| chr18:12688087 | C | CA | 3 | a0001c0001t0003g0010 a0001c0001t0003g0179 a0001c0001t0003g0180 |
6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.934-1638dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688087 | |||||||
| chr18:12688146 | G | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.934-1696C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688146 | |||||||
| chr18:12688156 | G | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-1706C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688156 | |||||||
| chr18:12688228 | C | CA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0070 a0001c0001t0002g0270 others(5): Show |
8 | HG01169.hp2 HG01361.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-1779dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688228 | |||||||
| chr18:12688228 | CA | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.934-1779delT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688228 | |||||||
| chr18:12688243 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0003g0180 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.934-1793T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688243 | |||||||
| chr18:12688279 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
23 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.934-1829C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688279 | |||||||
| chr18:12688390 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.934-1940A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688390 | |||||||
| chr18:12688423 | C | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1973G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688423 | |||||||
| chr18:12688609 | C | A | 2 | a0001c0001t0005g0049 a0001c0001t0005g0060 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.934-2159G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688609 | |||||||
| chr18:12688633 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.934-2183C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688633 | |||||||
| chr18:12688684 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.934-2234G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688684 | |||||||
| chr18:12688701 | A | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.934-2251T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688701 | |||||||
| chr18:12688729 | T | A | 1 | a0001c0001t0004g0185 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.934-2279A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688729 | |||||||
| chr18:12688880 | C | T | 1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.934-2430G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688880 | |||||||
| chr18:12688892 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
83 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.934-2442C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688892 | |||||||
| chr18:12688911 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02451.hp1 HG02486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.933+2448C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12688911 | |||||||
| chr18:12689014 | T | C | 60 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(57): Show |
81 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.933+2345A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689014 | |||||||
| chr18:12689280 | A | AAGC | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+2076_933+2078d others(5): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689280 | |||||||
| chr18:12689587 | T | TTCAG | 42 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0004 others(39): Show |
62 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.933+1771_933+1772i others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689587 | |||||||
| chr18:12689638 | T | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
12 | HG00280.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1721A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689638 | |||||||
| chr18:12689764 | T | TTA | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
16 | HG00280.hp1 HG00438.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.933+1593_933+1594d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689764 | |||||||
| chr18:12689782 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.933+1577T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689782 | |||||||
| chr18:12689786 | T | C | 7 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+1573A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689786 | |||||||
| chr18:12689859 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
26 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.933+1500G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689859 | |||||||
| chr18:12689866 | T | A | 1 | a0001c0001t0002g0248 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.933+1493A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689866 | |||||||
| chr18:12689911 | C | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+1448G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689911 | |||||||
| chr18:12689923 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.933+1436C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689923 | |||||||
| chr18:12689986 | G | A | 5 | a0001c0001t0005g0049 a0001c0001t0005g0057 a0001c0001t0005g0058 others(2): Show |
5 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+1373C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12689986 | |||||||
| chr18:12690030 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.933+1329G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690030 | |||||||
| chr18:12690078 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.933+1281G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690078 | |||||||
| chr18:12690080 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.933+1279G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690080 | |||||||
| chr18:12690085 | GGC | G | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.933+1272_933+1273d others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690085 | |||||||
| chr18:12690102 | C | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+1257G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690102 | |||||||
| chr18:12690163 | T | C | 1 | a0001c0001t0002g0045 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.933+1196A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690163 | |||||||
| chr18:12690375 | A | G | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.933+984T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690375 | |||||||
| chr18:12690462 | G | GT | 9 | a0001c0001t0001g0015 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
11 | HG01167.hp2 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.933+896dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690462 | |||||||
| chr18:12690462 | G | GTT | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.933+895_933+896dup others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690462 | |||||||
| chr18:12690478 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.933+881G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690478 | |||||||
| chr18:12690503 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.933+856G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690503 | |||||||
| chr18:12690504 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.933+855C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690504 | |||||||
| chr18:12690532 | T | C | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.933+827A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690532 | |||||||
| chr18:12690548 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.933+811G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690548 | |||||||
| chr18:12690581 | G | A | 2 | a0001c0001t0001g0050 a0003c0006t0001g0055 |
2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.933+778C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690581 | |||||||
| chr18:12690606 | C | T | 1 | a0001c0001t0003g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.933+753G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690606 | |||||||
| chr18:12690706 | C | T | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.933+653G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690706 | |||||||
| chr18:12690840 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.933+519A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690840 | |||||||
| chr18:12690939 | G | GC | 49 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0052 others(46): Show |
71 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.933+419dupG | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690939 | |||||||
| chr18:12690941 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.933+418G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12690941 | |||||||
| chr18:12691043 | G | GTTAAACA others(27): Show |
1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.933+282_933+315dup others(34): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 7/11 | chr18 | 12691043 | |||||||
| chr18:12691546 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.805-59A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691546 | |||||||
| chr18:12691558 | T | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18960.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.805-71A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691558 | |||||||
| chr18:12691611 | A | G | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.805-124T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691611 | |||||||
| chr18:12691630 | C | G | 1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805-143G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691630 | |||||||
| chr18:12691646 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.805-159G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691646 | |||||||
| chr18:12691684 | T | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.805-197A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691684 | |||||||
| chr18:12691709 | A | AT | 65 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(62): Show |
94 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.805-223dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691709 | |||||||
| chr18:12691817 | G | A | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.805-330C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691817 | |||||||
| chr18:12691875 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691875 | |||||||
| chr18:12691952 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.805-465G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691952 | |||||||
| chr18:12691961 | C | T | 7 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.805-474G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12691961 | |||||||
| chr18:12692038 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.805-551C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692038 | |||||||
| chr18:12692241 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
15 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-754C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692241 | |||||||
| chr18:12692265 | G | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.805-778C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692265 | |||||||
| chr18:12692273 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.805-786C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692273 | |||||||
| chr18:12692315 | C | CA | 20 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
28 | HG00597.hp2 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.805-829dupT | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692315 | |||||||
| chr18:12692373 | T | C | 1 | a0001c0001t0003g0176 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.805-886A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692373 | |||||||
| chr18:12692447 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0198 a0001c0001t0001g0199 others(3): Show |
8 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-960C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692447 | |||||||
| chr18:12692477 | A | G | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-990T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692477 | |||||||
| chr18:12692561 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.805-1074G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692561 | |||||||
| chr18:12692717 | G | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.805-1230C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12692717 | |||||||
| chr18:12693066 | C | T | 2 | a0001c0001t0004g0177 a0001c0001t0004g0178 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.805-1579G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693066 | |||||||
| chr18:12693334 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.805-1847C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693334 | |||||||
| chr18:12693656 | A | G | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+1598T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693656 | |||||||
| chr18:12693676 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.804+1578T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693676 | |||||||
| chr18:12693684 | G | A | 6 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(3): Show |
6 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+1570C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693684 | |||||||
| chr18:12693707 | C | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
27 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.804+1547G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693707 | |||||||
| chr18:12693736 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1518A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693736 | |||||||
| chr18:12693742 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1512G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693742 | |||||||
| chr18:12693746 | GCACTCCA others(39): Show |
G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1462_804+1507d others(48): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693746 | |||||||
| chr18:12693768 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.804+1486G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693768 | |||||||
| chr18:12693805 | T | A | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.804+1449A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693805 | |||||||
| chr18:12693852 | A | ATGTATAT others(6): Show |
1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1401_804+1402i others(15): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693852 | |||||||
| chr18:12693853 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1401C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12693853 | |||||||
| chr18:12694058 | GCTGGACT others(18): Show |
G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1171_804+1195d others(27): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694058 | |||||||
| chr18:12694085 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1169A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694085 | |||||||
| chr18:12694089 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1165G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694089 | |||||||
| chr18:12694090 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1164G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694090 | |||||||
| chr18:12694122 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1132T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694122 | |||||||
| chr18:12694133 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1121A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694133 | |||||||
| chr18:12694137 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1117G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694137 | |||||||
| chr18:12694138 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0119 |
2 | HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.804+1116T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694138 | |||||||
| chr18:12694143 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1111C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694143 | |||||||
| chr18:12694159 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1095T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694159 | |||||||
| chr18:12694162 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1092G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694162 | |||||||
| chr18:12694174 | C | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1080G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694174 | |||||||
| chr18:12694175 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1079T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694175 | |||||||
| chr18:12694180 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1074T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694180 | |||||||
| chr18:12694182 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1072T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694182 | |||||||
| chr18:12694185 | C | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1069G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694185 | |||||||
| chr18:12694191 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1063T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694191 | |||||||
| chr18:12694196 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1058T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694196 | |||||||
| chr18:12694216 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1038T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694216 | |||||||
| chr18:12694224 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1030T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694224 | |||||||
| chr18:12694228 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1026T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694228 | |||||||
| chr18:12694239 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.804+1015T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694239 | |||||||
| chr18:12694257 | G | T | 1 | a0001c0001t0005g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.804+997C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694257 | |||||||
| chr18:12694285 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.804+969A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694285 | |||||||
| chr18:12694368 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.804+886T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694368 | |||||||
| chr18:12694380 | G | A | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+874C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694380 | |||||||
| chr18:12694530 | G | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+724C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694530 | |||||||
| chr18:12694708 | C | CT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | NA18940.hp2 NA19002.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+545dupA | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694708 | |||||||
| chr18:12694734 | T | TG | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.804+519dupC | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694734 | |||||||
| chr18:12694867 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.804+387G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694867 | |||||||
| chr18:12694935 | A | T | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+319T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694935 | |||||||
| chr18:12694939 | T | G | 1 | a0001c0001t0003g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.804+315A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694939 | |||||||
| chr18:12694986 | A | G | 71 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(68): Show |
95 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.804+268T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694986 | |||||||
| chr18:12694995 | G | A | 20 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0065 others(17): Show |
25 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.804+259C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694995 | |||||||
| chr18:12694997 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.804+257C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12694997 | |||||||
| chr18:12695027 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.804+227G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12695027 | |||||||
| chr18:12695087 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.804+167T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 6/11 | chr18 | 12695087 | |||||||
| chr18:12695416 | C | A | 38 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(35): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.707-65G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695416 | |||||||
| chr18:12695652 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0189 a0004c0004t0001g0188 |
5 | HG01884.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-301T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695652 | |||||||
| chr18:12695852 | C | CCA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(74): Show |
97 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.707-503_707-502dup others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | C | CCACA | 43 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(40): Show |
65 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.707-505_707-502dup others(4): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | C | CCACACA | 11 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0085 others(8): Show |
12 | HG01168.hp1 HG01928.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.707-507_707-502dup others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | C | CCACACAC others(1): Show |
11 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0086 others(8): Show |
13 | HG00639.hp1 HG00741.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.707-509_707-502dup others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | C | CCACACAC others(3): Show |
1 | a0001c0001t0001g0025 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.707-511_707-502dup others(10): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | CCA | C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
26 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.707-503_707-502del others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | CCACACA | C | 12 | a0001c0001t0003g0010 a0001c0001t0003g0179 a0001c0001t0003g0180 others(9): Show |
16 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.707-507_707-502del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695852 | CCACACAC others(1): Show |
C | 5 | a0001c0001t0003g0035 a0001c0001t0003g0176 a0001c0001t0005g0057 others(2): Show |
6 | HG02486.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-509_707-502del others(8): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695852 | |||||||
| chr18:12695867 | C | G | 1 | a0001c0001t0005g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.707-516G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695867 | |||||||
| chr18:12695886 | T | A | 1 | a0001c0001t0001g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.707-535A>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12695886 | |||||||
| chr18:12696124 | G | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | NA18944.hp1 NA18969.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.707-773C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696124 | |||||||
| chr18:12696232 | G | A | 15 | a0001c0001t0003g0010 a0001c0001t0003g0035 a0001c0001t0003g0065 others(12): Show |
20 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.707-881C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696232 | |||||||
| chr18:12696449 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.706+774C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696449 | |||||||
| chr18:12696502 | A | AAAT | 7 | a0001c0001t0005g0049 a0001c0001t0005g0056 a0001c0001t0005g0057 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.706+718_706+720dup others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | |||||||
| chr18:12696502 | AAAT | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.706+718_706+720del others(3): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | |||||||
| chr18:12696502 | AAATAAT | A | 16 | a0001c0001t0001g0175 a0001c0001t0003g0010 a0001c0001t0003g0035 others(13): Show |
21 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.706+715_706+720del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696502 | |||||||
| chr18:12696593 | G | A | 1 | a0001c0001t0005g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.706+630C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696593 | |||||||
| chr18:12696871 | T | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0047 others(13): Show |
24 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.706+352A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696871 | |||||||
| chr18:12696930 | CTTATAT | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+287_706+292del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696930 | |||||||
| chr18:12696993 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | NA19065.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.706+230T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12696993 | |||||||
| chr18:12697082 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.706+141A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697082 | |||||||
| chr18:12697084 | A | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.706+139T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697084 | |||||||
| chr18:12697109 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.706+114A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697109 | |||||||
| chr18:12697207 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA18967.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.706+16T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 5/11 | chr18 | 12697207 | |||||||
| chr18:12697712 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.521-304T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697712 | |||||||
| chr18:12697776 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.521-368G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697776 | |||||||
| chr18:12697796 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0243 |
4 | HG02258.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-388A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697796 | |||||||
| chr18:12697819 | G | GC | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-412dupG | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697819 | |||||||
| chr18:12697821 | A | T | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-413T>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697821 | |||||||
| chr18:12697826 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.521-418C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697826 | |||||||
| chr18:12697975 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.521-567G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12697975 | |||||||
| chr18:12698080 | C | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0047 others(13): Show |
24 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.521-672G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698080 | |||||||
| chr18:12698158 | TTATTTA | T | 13 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(10): Show |
14 | HG00639.hp1 HG02055.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.521-756_521-751del others(6): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698158 | |||||||
| chr18:12698205 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.520+774A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698205 | |||||||
| chr18:12698365 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG02257.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.520+614G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698365 | |||||||
| chr18:12698459 | A | G | 1 | a0003c0006t0001g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.520+520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698459 | |||||||
| chr18:12698607 | C | T | 72 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.520+372G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 4/11 | chr18 | 12698607 | |||||||
| chr18:12699268 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-65A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 3/11 | chr18 | 12699268 | |||||||
| chr18:12699287 | C | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
14 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-84G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 3/11 | chr18 | 12699287 | |||||||
| chr18:12699913 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | splice_region_variant&intron_variant | LOW | c.220-8C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12699913 | |||||||
| chr18:12700093 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.220-188T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700093 | |||||||
| chr18:12700198 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.220-293A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700198 | |||||||
| chr18:12700311 | A | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG00639.hp1 HG02055.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-406T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700311 | |||||||
| chr18:12700376 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220-471T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700376 | |||||||
| chr18:12700513 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.219+445A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700513 | |||||||
| chr18:12700690 | C | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(64): Show |
98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.219+268G>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700690 | |||||||
| chr18:12700850 | G | A | 72 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.219+108C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700850 | |||||||
| chr18:12700906 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.219+52C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700906 | |||||||
| chr18:12700919 | CATAT | C | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0019 others(37): Show |
60 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.219+35_219+38delAT others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 2/11 | chr18 | 12700919 | |||||||
| chr18:12701327 | A | C | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(41): Show |
64 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.64-214T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701327 | |||||||
| chr18:12701444 | T | G | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-331A>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701444 | |||||||
| chr18:12701453 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-340C>T | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701453 | |||||||
| chr18:12701555 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.64-442A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701555 | |||||||
| chr18:12701633 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-520T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701633 | |||||||
| chr18:12701662 | GCACT | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | NA19002.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.64-553_64-550delAG others(2): Show |
CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701662 | |||||||
| chr18:12701762 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
5 | HG02055.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-649T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701762 | |||||||
| chr18:12701938 | C | G | 72 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(69): Show |
96 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.63+548G>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12701938 | |||||||
| chr18:12702081 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.63+405C>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702081 | |||||||
| chr18:12702124 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.63+362T>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702124 | |||||||
| chr18:12702146 | T | C | 1 | a0001c0001t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.63+340A>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702146 | |||||||
| chr18:12702218 | C | T | 1 | a0001c0001t0005g0049 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+268G>A | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702218 | |||||||
| chr18:12702374 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.63+112T>C | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702374 | |||||||
| chr18:12702433 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.63+53C>G | CEP76 | ENSG00000101624.11 | transcript | ENST00000262127.7 | protein_coding | 1/11 | chr18 | 12702433 |