Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64793 |
| ensemblid | ENSG00000130695.16 |
| hgncid | 25309 |
| symbol | CEP85 |
| name | centrosomal protein 85 |
| refseq_nuc | NM_001319944.2 |
| refseq_prot | NP_001306873.1 |
| ensembl_nuc | ENST00000451429.8 |
| ensembl_prot | ENSP00000417002.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 26234200 |
| end | 26278808 |
| strand | + |
| ver | v1.2 |
| region | chr1:26234200-26278808 |
| region5000 | chr1:26229200-26283808 |
| regionname0 | CEP85_chr1_26234200_26278808 |
| regionname5000 | CEP85_chr1_26229200_26283808 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 761 | 226 | 56 | 42 | 95 | 6 | 25 | 78 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0002 | 0/0 | 761 | 73 | 4 | 17 | 43 | 4 | 5 | 31 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0003 | 0/0 | 761 | 28 | 12 | 4 | 1 | 6 | 5 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0004 | 0/0 | 761 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0005 | 0/0 | 761 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0006 | 0/0 | 761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0007 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0008 | 0/0 | 761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0009 | 0/0 | 761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| a0010 | 0/0 | 761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | MAMQE others(756): Show |
chr1 | 26229200 | 26283808 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2283 | 223 | 55 | 40 | 95 | 6 | 25 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0001c0009 | 0/0 | 2283 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0001c0016 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0002c0002 | 0/0 | 2283 | 72 | 4 | 16 | 43 | 4 | 5 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0002c0012 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0003c0003 | 0/0 | 2283 | 21 | 7 | 4 | 1 | 6 | 3 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0003c0005 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0003c0007 | 0/0 | 2283 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0003c0008 | 0/0 | 2283 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0004c0004 | 0/0 | 2283 | 5 | 5 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0004c0010 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0004c0011 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0005c0006 | 0/0 | 2283 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0006c0014 | 0/0 | 2283 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0007c0018 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0008c0013 | 0/0 | 2283 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0009c0015 | 0/0 | 2283 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 | ||
| a0010c0017 | 0/0 | 2283 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | ATGGC others(2278): Show |
chr1 | 26229200 | 26283808 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3934 | 48 | 20 | 12 | 5 | 5 | 6 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0001t0002 | 1/0 | 3934 | 84 | 10 | 4 | 59 | 0 | 10 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0001t0003 | 0/1 | 3934 | 71 | 24 | 10 | 27 | 1 | 8 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0001t0005 | 0/0 | 3934 | 18 | 0 | 14 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0001t0009 | 0/0 | 3934 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0001t0012 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0009t0003 | 0/0 | 3934 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0001c0016t0011 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0002c0002t0001 | 0/0 | 3934 | 67 | 4 | 16 | 38 | 4 | 5 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0002c0002t0007 | 0/0 | 3934 | 4 | 0 | 0 | 4 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0002c0002t0010 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0002c0012t0001 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0003c0003t0004 | 0/0 | 3936 | 17 | 7 | 2 | 1 | 4 | 3 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| a0003c0003t0006 | 0/0 | 3936 | 4 | 0 | 2 | 0 | 2 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| a0003c0005t0004 | 0/0 | 3936 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| a0003c0007t0004 | 0/0 | 3936 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| a0003c0008t0004 | 0/0 | 3936 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| a0004c0004t0003 | 0/0 | 3934 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0004c0004t0008 | 0/0 | 3934 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0004c0010t0003 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0004c0011t0008 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0005c0006t0001 | 0/0 | 3934 | 3 | 3 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0006c0014t0002 | 0/0 | 3934 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0007c0018t0003 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0008c0013t0005 | 0/0 | 3934 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0009c0015t0003 | 0/0 | 3934 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3929): Show |
chr1 | 26229200 | 26283808 |
| a0010c0017t0004 | 0/0 | 3936 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | GTGCA others(3931): Show |
chr1 | 26229200 | 26283808 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0001 | 0/0 | 13 | 0 | 3 | 9 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0008 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0009t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0009t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0001c0016t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0007g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0002t0010g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0002c0012t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0006g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0003t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0005t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0005t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0005t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0007t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0007t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0008t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0003c0008t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0004t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0004t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0004t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0004t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0010t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0004c0011t0008g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0005c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0005c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0005c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0006c0014t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0007c0018t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0008c0013t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0009c0015t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| a0010c0017t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0230 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00140 | hp2 | a0003 | c0003 | t0004 | g0294 | EUR | GBR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0220 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00280 | hp2 | a0003 | c0003 | t0006 | g0094 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00323 | hp1 | a0003 | c0003 | t0004 | g0287 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0107 | EUR | FIN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00558 | hp1 | a0006 | c0014 | t0002 | g0067 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00621 | hp2 | a0002 | c0002 | t0010 | g0270 | EAS | CHS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00639 | hp1 | a0004 | c0011 | t0008 | g0276 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0027 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00733 | hp1 | a0003 | c0003 | t0006 | g0095 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00741 | hp1 | a0003 | c0003 | t0004 | g0295 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01069 | hp2 | a0001 | c0009 | t0003 | g0108 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01071 | hp2 | a0001 | c0009 | t0003 | g0111 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01192 | hp2 | a0007 | c0018 | t0003 | g0123 | AMR | PUR | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01361 | hp1 | a0003 | c0003 | t0006 | g0096 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01515 | hp1 | a0003 | c0003 | t0006 | g0093 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0212 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01516 | hp2 | a0003 | c0003 | t0004 | g0300 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01517 | hp1 | a0003 | c0003 | t0004 | g0293 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01934 | hp1 | a0008 | c0013 | t0005 | g0002 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0034 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02004 | hp2 | a0003 | c0003 | t0004 | g0017 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02056 | hp1 | a0002 | c0002 | t0007 | g0268 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02080 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | CDX | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02257 | hp2 | a0004 | c0004 | t0003 | g0277 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02300 | hp2 | a0001 | c0001 | t0005 | g0083 | AMR | PEL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02572 | hp1 | a0003 | c0003 | t0004 | g0301 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02615 | hp1 | a0004 | c0004 | t0003 | g0281 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02622 | hp2 | a0003 | c0005 | t0004 | g0305 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02630 | hp2 | a0005 | c0006 | t0001 | g0248 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02647 | hp1 | a0003 | c0007 | t0004 | g0303 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02647 | hp2 | a0005 | c0006 | t0001 | g0265 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02683 | hp2 | a0003 | c0003 | t0004 | g0302 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02723 | hp1 | a0004 | c0010 | t0003 | g0275 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02809 | hp1 | a0001 | c0016 | t0011 | g0307 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02895 | hp2 | a0005 | c0006 | t0001 | g0247 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02896 | hp1 | a0003 | c0003 | t0004 | g0286 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02896 | hp2 | a0003 | c0005 | t0004 | g0306 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02897 | hp2 | a0003 | c0003 | t0004 | g0285 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02976 | hp2 | a0009 | c0015 | t0003 | g0163 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03041 | hp1 | a0003 | c0003 | t0004 | g0288 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03195 | hp1 | a0003 | c0005 | t0004 | g0282 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03486 | hp2 | a0003 | c0003 | t0004 | g0299 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03491 | hp1 | a0003 | c0008 | t0004 | g0292 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03492 | hp2 | a0003 | c0008 | t0004 | g0291 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03516 | hp1 | a0004 | c0004 | t0008 | g0279 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | MSL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0228 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03710 | hp2 | a0003 | c0003 | t0004 | g0017 | SAS | PJL | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04115 | hp1 | a0010 | c0017 | t0004 | g0289 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04199 | hp1 | a0003 | c0003 | t0004 | g0297 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0233 | SAS | STU | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18522 | hp2 | a0003 | c0003 | t0004 | g0308 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18612 | hp2 | a0002 | c0002 | t0007 | g0005 | EAS | CHB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18906 | hp2 | a0004 | c0004 | t0008 | g0278 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18960 | hp2 | a0002 | c0002 | t0007 | g0014 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19030 | hp2 | a0003 | c0003 | t0004 | g0296 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19043 | hp1 | a0004 | c0004 | t0003 | g0280 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19080 | hp1 | a0003 | c0003 | t0004 | g0290 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19083 | hp2 | a0002 | c0002 | t0007 | g0207 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ASW | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0206 | EUR | TSI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG01123 | hp2 | a0002 | c0012 | t0001 | g0188 | AMR | CLM | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG02486 | hp2 | a0003 | c0007 | t0004 | g0304 | AFR | ACB | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | USA | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0141 | REF | REF | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0008 | REF | REF | CEP85_chr1_26229200_26283808 | CEP85 | chr1 | 26229200 | 26283808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:26244166 | G | T | 1 | a0007 | 1 | HG01192.hp2 | missense_variant&splice_region_variant | MODERATE | c.56G>T | p.Ser19Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 189/3934 | 56/2286 | 19/761 | chr1 | 26244166 | |||
| chr1:26244205 | A | G | 1 | a0010 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.95A>G | p.Glu32Gly | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 228/3934 | 95/2286 | 32/761 | chr1 | 26244205 | |||
| chr1:26244253 | G | A | 1 | a0004 | 7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
missense_variant | MODERATE | c.143G>A | p.Arg48His | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 276/3934 | 143/2286 | 48/761 | chr1 | 26244253 | |||
| chr1:26255600 | G | A | 1 | a0002 | 73 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(70): Show |
missense_variant | MODERATE | c.638G>A | p.Ser213Asn | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 771/3934 | 638/2286 | 213/761 | chr1 | 26255600 | |||
| chr1:26255849 | A | G | 1 | a0005 | 3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
missense_variant | MODERATE | c.887A>G | p.Gln296Arg | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 1020/3934 | 887/2286 | 296/761 | chr1 | 26255849 | |||
| chr1:26258178 | T | C | 1 | a0008 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1073T>C | p.Val358Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/14 | 1206/3934 | 1073/2286 | 358/761 | chr1 | 26258178 | |||
| chr1:26259676 | G | T | 1 | a0009 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1215G>T | p.Leu405Phe | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1348/3934 | 1215/2286 | 405/761 | chr1 | 26259676 | |||
| chr1:26269589 | G | A | 2 | a0003 a0010 |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
missense_variant | MODERATE | c.1624G>A | p.Ala542Thr | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/14 | 1757/3934 | 1624/2286 | 542/761 | chr1 | 26269589 | |||
| chr1:26269604 | G | A | 1 | a0006 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1639G>A | p.Ala547Thr | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/14 | 1772/3934 | 1639/2286 | 547/761 | chr1 | 26269604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:26244269 | C | A | 1 | a0004c0010 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.159C>A | p.Ala53Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/14 | 292/3934 | 159/2286 | 53/761 | chr1 | 26244269 | |||
| chr1:26255490 | G | A | 2 | a0003c0005 a0003c0007 |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
synonymous_variant | LOW | c.528G>A | p.Ala176Ala | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 661/3934 | 528/2286 | 176/761 | chr1 | 26255490 | |||
| chr1:26255769 | G | A | 1 | a0003c0008 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.807G>A | p.Pro269Pro | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/14 | 940/3934 | 807/2286 | 269/761 | chr1 | 26255769 | |||
| chr1:26257653 | C | A | 1 | a0003c0007 | 2 | HG02486.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.960C>A | p.Ile320Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/14 | 1093/3934 | 960/2286 | 320/761 | chr1 | 26257653 | |||
| chr1:26257680 | C | T | 1 | a0001c0009 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.987C>T | p.Ile329Ile | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/14 | 1120/3934 | 987/2286 | 329/761 | chr1 | 26257680 | |||
| chr1:26259619 | A | G | 1 | a0001c0016 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.1158A>G | p.Glu386Glu | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1291/3934 | 1158/2286 | 386/761 | chr1 | 26259619 | |||
| chr1:26259652 | G | A | 1 | a0002c0012 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1191G>A | p.Gln397Gln | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/14 | 1324/3934 | 1191/2286 | 397/761 | chr1 | 26259652 | |||
| chr1:26271047 | T | C | 1 | a0004c0011 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.1683T>C | p.Ser561Ser | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/14 | 1816/3934 | 1683/2286 | 561/761 | chr1 | 26271047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:26234243 | A | G | 1 | a0001c0001t0012 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-90A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/14 | 5541 | chr1 | 26234243 | ||||||
| chr1:26234254 | G | A | 10 | a0001c0001t0003 a0001c0001t0012 a0001c0009t0003 others(7): Show |
86 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/14 | 5530 | chr1 | 26234254 | ||||||
| chr1:26277392 | G | GAA | 6 | a0003c0003t0004 a0003c0003t0006 a0003c0005t0004 others(3): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*99_*100insAA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 100 | chr1 | 26277392 | ||||||
| chr1:26277502 | A | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0012 others(19): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*209A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 209 | chr1 | 26277502 | ||||||
| chr1:26277580 | T | G | 6 | a0003c0003t0004 a0003c0003t0006 a0003c0005t0004 others(3): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*287T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 287 | chr1 | 26277580 | ||||||
| chr1:26277865 | G | A | 1 | a0002c0002t0010 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 572 | chr1 | 26277865 | ||||||
| chr1:26277880 | G | A | 1 | a0001c0001t0009 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 587 | chr1 | 26277880 | ||||||
| chr1:26277900 | C | A | 2 | a0004c0004t0008 a0004c0011t0008 |
3 | HG00639.hp1 HG03516.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*607C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 607 | chr1 | 26277900 | ||||||
| chr1:26278031 | C | A | 2 | a0001c0001t0005 a0008c0013t0005 |
19 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 738 | chr1 | 26278031 | ||||||
| chr1:26278450 | G | A | 1 | a0002c0002t0007 | 4 | HG02056.hp1 NA18612.hp2 NA18960.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1157 | chr1 | 26278450 | ||||||
| chr1:26278578 | T | C | 6 | a0003c0003t0004 a0003c0003t0006 a0003c0005t0004 others(3): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1285T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1285 | chr1 | 26278578 | ||||||
| chr1:26278650 | C | T | 1 | a0001c0016t0011 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 14/14 | 1357 | chr1 | 26278650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:26234454 | C | G | 230 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-23+144C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234454 | |||||||
| chr1:26234471 | C | T | 25 | a0001c0001t0001g0298 a0001c0016t0011g0307 a0003c0003t0004g0017 others(22): Show |
26 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23+161C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234471 | |||||||
| chr1:26234596 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+286C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234596 | |||||||
| chr1:26234705 | A | G | 1 | a0003c0003t0004g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-23+395A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234705 | |||||||
| chr1:26234729 | G | C | 77 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(74): Show |
79 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-23+419G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234729 | |||||||
| chr1:26234749 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-23+439G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234749 | |||||||
| chr1:26234952 | G | A | 1 | a0001c0001t0003g0092 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-23+642G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234952 | |||||||
| chr1:26234970 | A | G | 1 | a0003c0005t0004g0282 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-23+660A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26234970 | |||||||
| chr1:26235268 | C | T | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+958C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235268 | |||||||
| chr1:26235310 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0274 |
3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-23+1000A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235310 | |||||||
| chr1:26235326 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | HG00597.hp1 NA18960.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-23+1016T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235326 | |||||||
| chr1:26235365 | T | C | 28 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-23+1055T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235365 | |||||||
| chr1:26235393 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-23+1083G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235393 | |||||||
| chr1:26235540 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-23+1230A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235540 | |||||||
| chr1:26235564 | A | ATTTTTTT others(3): Show |
1 | a0003c0005t0004g0306 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-23+1256_-23+1257i others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235564 | ||||||
| chr1:26235567 | C | CT | 42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(39): Show |
45 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23+1277dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTT | 135 | a0001c0001t0001g0208 a0001c0001t0001g0235 a0001c0001t0001g0250 others(132): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-23+1276_-23+1277d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTT | 12 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0164 others(9): Show |
12 | HG00621.hp2 HG02056.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-23+1275_-23+1277d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(3): Show |
9 | a0003c0003t0004g0017 a0003c0003t0004g0286 a0003c0003t0004g0287 others(6): Show |
10 | HG00323.hp1 HG01515.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+1268_-23+1277d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(4): Show |
9 | a0001c0001t0001g0298 a0003c0003t0004g0293 a0003c0003t0004g0294 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+1267_-23+1277d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(5): Show |
2 | a0003c0003t0004g0300 a0003c0003t0006g0096 |
2 | HG01361.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-23+1266_-23+1277d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0012g0168 a0003c0003t0004g0301 a0003c0003t0004g0302 |
3 | HG02486.hp1 HG02572.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-23+1265_-23+1277d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0271 a0004c0011t0008g0276 |
2 | HG00639.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-23+1261_-23+1277d others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(11): Show |
5 | a0001c0001t0001g0272 a0004c0004t0003g0277 a0004c0004t0003g0280 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1260_-23+1277d others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | CTTTTTTT others(14): Show |
1 | a0004c0004t0003g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+1277_-23+1278i others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26235567 | ||||||
| chr1:26235567 | C | T | 5 | a0002c0002t0001g0273 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+1257C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235567 | |||||||
| chr1:26235813 | C | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-23+1503C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26235813 | |||||||
| chr1:26236023 | G | A | 1 | a0001c0001t0002g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-23+1713G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236023 | |||||||
| chr1:26236152 | C | T | 2 | a0003c0008t0004g0291 a0003c0008t0004g0292 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-23+1842C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236152 | |||||||
| chr1:26236240 | G | T | 1 | a0001c0001t0005g0083 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-23+1930G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236240 | |||||||
| chr1:26236270 | T | C | 308 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(305): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-23+1960T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236270 | |||||||
| chr1:26236394 | C | CT | 21 | a0001c0001t0001g0205 a0001c0001t0001g0271 a0001c0001t0001g0272 others(18): Show |
21 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-23+2097dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26236394 | ||||||
| chr1:26236407 | T | C | 17 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(14): Show |
19 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+2097T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236407 | |||||||
| chr1:26236408 | C | T | 219 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(216): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-23+2098C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236408 | |||||||
| chr1:26236614 | G | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-23+2304G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236614 | |||||||
| chr1:26236923 | G | A | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+2613G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26236923 | |||||||
| chr1:26237174 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0274 |
3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-22-2588G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237174 | |||||||
| chr1:26237205 | T | G | 1 | a0002c0002t0001g0273 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-22-2557T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237205 | |||||||
| chr1:26237252 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-22-2510C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237252 | |||||||
| chr1:26237359 | T | G | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.-22-2403T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237359 | |||||||
| chr1:26237416 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-22-2346A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237416 | |||||||
| chr1:26237441 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-2321A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237441 | |||||||
| chr1:26237621 | T | C | 3 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0003g0101 |
3 | HG00639.hp2 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-22-2141T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237621 | |||||||
| chr1:26237739 | C | A | 28 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-2023C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237739 | |||||||
| chr1:26237755 | T | C | 1 | a0001c0001t0005g0023 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-22-2007T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237755 | |||||||
| chr1:26237805 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-22-1957C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26237805 | |||||||
| chr1:26238067 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-22-1695T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238067 | |||||||
| chr1:26238202 | C | CTTTTTT | 27 | a0001c0001t0001g0176 a0001c0001t0001g0284 a0001c0001t0003g0103 others(24): Show |
28 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.-22-1549_-22-1544d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | ||||||
| chr1:26238202 | C | CTTTTTTT | 160 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(157): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.-22-1550_-22-1544d others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | ||||||
| chr1:26238202 | C | CTTTTTTT others(1): Show |
33 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(30): Show |
33 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-22-1551_-22-1544d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 26238202 | ||||||
| chr1:26238344 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-22-1418G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238344 | |||||||
| chr1:26238347 | C | T | 28 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-22-1415C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238347 | |||||||
| chr1:26238389 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-22-1373C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238389 | |||||||
| chr1:26238415 | C | T | 6 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0003g0101 others(3): Show |
6 | HG00639.hp2 HG01099.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-22-1347C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238415 | |||||||
| chr1:26238447 | C | T | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-22-1315C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238447 | |||||||
| chr1:26238478 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-22-1284G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238478 | |||||||
| chr1:26238492 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-22-1270G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26238492 | |||||||
| chr1:26239174 | G | A | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-22-588G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239174 | |||||||
| chr1:26239355 | T | A | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-22-407T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239355 | |||||||
| chr1:26239534 | T | C | 1 | a0002c0002t0001g0209 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-22-228T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239534 | |||||||
| chr1:26239551 | CATGTTGG others(56): Show |
C | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-22-210_-22-148del others(63): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239551 | |||||||
| chr1:26239599 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-22-163G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239599 | |||||||
| chr1:26239696 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
6 | HG00140.hp1 HG01496.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-66G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 1/13 | chr1 | 26239696 | |||||||
| chr1:26240126 | A | G | 1 | a0002c0002t0001g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.55+288A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240126 | |||||||
| chr1:26240194 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.55+356A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240194 | |||||||
| chr1:26240275 | C | T | 2 | a0002c0002t0001g0258 a0002c0002t0001g0263 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.55+437C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240275 | |||||||
| chr1:26240378 | C | T | 3 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | HG02129.hp2 NA18954.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.55+540C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240378 | |||||||
| chr1:26240422 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55+584G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240422 | |||||||
| chr1:26240553 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+715A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240553 | |||||||
| chr1:26240751 | C | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.55+913C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240751 | |||||||
| chr1:26240774 | A | T | 1 | a0004c0004t0003g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55+936A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240774 | |||||||
| chr1:26240869 | G | A | 1 | a0001c0001t0005g0024 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.55+1031G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240869 | |||||||
| chr1:26240894 | T | C | 1 | a0002c0002t0001g0210 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.55+1056T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240894 | |||||||
| chr1:26240913 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55+1075A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26240913 | |||||||
| chr1:26241163 | A | G | 1 | a0003c0003t0004g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.55+1325A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241163 | |||||||
| chr1:26241243 | A | ATTTTTTT others(5): Show |
23 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0287 others(20): Show |
24 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.55+1405_55+1406ins others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241243 | |||||||
| chr1:26241243 | A | ATTTTTTT others(6): Show |
6 | a0003c0003t0004g0285 a0003c0003t0004g0286 a0003c0003t0004g0296 others(3): Show |
6 | HG01361.hp1 HG01515.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.55+1405_55+1406ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241243 | |||||||
| chr1:26241244 | A | ATTTTTTT others(2): Show |
6 | a0001c0001t0003g0106 a0001c0001t0003g0107 a0002c0002t0001g0211 others(3): Show |
6 | HG00323.hp2 HG01516.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+1414_55+1422dup others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | ||||||
| chr1:26241244 | A | ATTTTTTT others(3): Show |
143 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0169 others(140): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.55+1413_55+1422dup others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | ||||||
| chr1:26241244 | A | ATTTTTTT others(4): Show |
39 | a0001c0001t0001g0010 a0001c0001t0001g0176 a0001c0001t0001g0178 others(36): Show |
40 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.55+1412_55+1422dup others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | ||||||
| chr1:26241244 | A | ATTTTTTT others(5): Show |
6 | a0001c0001t0001g0175 a0001c0001t0001g0256 a0001c0001t0001g0271 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.55+1411_55+1422dup others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26241244 | ||||||
| chr1:26241244 | A | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1406A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241244 | |||||||
| chr1:26241318 | C | T | 1 | a0001c0001t0003g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.55+1480C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241318 | |||||||
| chr1:26241389 | C | G | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.55+1551C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241389 | |||||||
| chr1:26241392 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.55+1554G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241392 | |||||||
| chr1:26241411 | T | A | 2 | a0003c0003t0004g0293 a0003c0003t0004g0300 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.55+1573T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241411 | |||||||
| chr1:26241446 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1608A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241446 | |||||||
| chr1:26241502 | G | A | 5 | a0001c0001t0003g0106 a0001c0001t0003g0109 a0001c0001t0003g0110 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.55+1664G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241502 | |||||||
| chr1:26241674 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.55+1836A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241674 | |||||||
| chr1:26241839 | G | C | 1 | a0002c0002t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.55+2001G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241839 | |||||||
| chr1:26241971 | A | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.55+2133A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26241971 | |||||||
| chr1:26242032 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56-2134G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242032 | |||||||
| chr1:26242051 | T | C | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.56-2115T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242051 | |||||||
| chr1:26242207 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-1959A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242207 | |||||||
| chr1:26242224 | G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.56-1942G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242224 | |||||||
| chr1:26242421 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-1745G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242421 | |||||||
| chr1:26242435 | G | A | 22 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(19): Show |
23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-1731G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242435 | |||||||
| chr1:26242539 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.56-1627G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242539 | |||||||
| chr1:26242637 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.56-1529G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242637 | |||||||
| chr1:26242794 | T | TTTTG | 215 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(212): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.56-1360_56-1357dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26242794 | ||||||
| chr1:26242976 | T | C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0189 others(2): Show |
5 | HG01255.hp1 HG02280.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.56-1190T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242976 | |||||||
| chr1:26242988 | C | T | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-1178C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26242988 | |||||||
| chr1:26243020 | G | T | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.56-1146G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243020 | |||||||
| chr1:26243025 | C | A | 2 | a0003c0008t0004g0291 a0003c0008t0004g0292 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.56-1141C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243025 | |||||||
| chr1:26243120 | G | A | 230 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.56-1046G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243120 | |||||||
| chr1:26243128 | CTT | C | 217 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.56-1020_56-1019del others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243128 | ||||||
| chr1:26243131 | T | C | 2 | a0003c0007t0004g0303 a0003c0007t0004g0304 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.56-1035T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243131 | |||||||
| chr1:26243132 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.56-1034T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243132 | |||||||
| chr1:26243194 | G | A | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.56-972G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243194 | |||||||
| chr1:26243208 | C | A | 1 | a0001c0001t0003g0161 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.56-958C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243208 | |||||||
| chr1:26243293 | G | A | 1 | a0002c0002t0001g0216 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.56-873G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243293 | |||||||
| chr1:26243311 | GTCTTGGT others(3): Show |
G | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.56-854_56-845delTC others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243311 | |||||||
| chr1:26243312 | T | G | 153 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(150): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.56-854T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243312 | |||||||
| chr1:26243330 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.56-836G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243330 | |||||||
| chr1:26243476 | A | G | 11 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(8): Show |
13 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.56-690A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243476 | |||||||
| chr1:26243499 | C | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.56-667C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243499 | |||||||
| chr1:26243518 | G | A | 22 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(19): Show |
23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.56-648G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243518 | |||||||
| chr1:26243770 | C | T | 8 | a0001c0001t0003g0098 a0001c0001t0003g0136 a0001c0001t0003g0137 others(5): Show |
8 | HG02258.hp2 HG02622.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.56-396C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243770 | |||||||
| chr1:26243825 | G | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.56-341G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243825 | |||||||
| chr1:26243927 | G | A | 3 | a0001c0001t0003g0146 a0001c0001t0003g0147 a0001c0001t0003g0159 |
3 | HG01099.hp2 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.56-239G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243927 | |||||||
| chr1:26243969 | G | T | 1 | a0002c0002t0001g0249 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.56-197G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | chr1 | 26243969 | |||||||
| chr1:26243991 | C | CA | 41 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0002g0037 others(38): Show |
41 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.56-149dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | C | CAA | 26 | a0001c0001t0001g0298 a0001c0001t0003g0109 a0001c0001t0003g0110 others(23): Show |
27 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.56-150_56-149dupAA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | C | CAAA | 9 | a0001c0009t0003g0108 a0003c0003t0004g0285 a0003c0003t0004g0286 others(6): Show |
9 | HG00323.hp1 HG01069.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-151_56-149dupAA others(1): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | C | CAAAA | 9 | a0001c0001t0001g0271 a0001c0001t0003g0106 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.56-152_56-149dupAA others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | CA | C | 9 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(6): Show |
9 | HG00544.hp2 HG02040.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.56-149delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0208 a0002c0002t0001g0210 |
2 | NA18961.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.56-158_56-149delAA others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26243991 | CAAAAAAA others(4): Show |
C | 109 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(106): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.56-159_56-149delAA others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 26243991 | ||||||
| chr1:26244465 | C | G | 11 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(8): Show |
13 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.208+147C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244465 | |||||||
| chr1:26244502 | T | A | 108 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(105): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.208+184T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244502 | |||||||
| chr1:26244601 | G | A | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.208+283G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244601 | |||||||
| chr1:26244714 | C | T | 1 | a0002c0002t0001g0273 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.208+396C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244714 | |||||||
| chr1:26244992 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208+674C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244992 | |||||||
| chr1:26244999 | A | G | 1 | a0002c0002t0010g0270 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+681A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26244999 | |||||||
| chr1:26245187 | A | AT | 186 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(183): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.208+883dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | ||||||
| chr1:26245187 | A | ATT | 8 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0003g0097 others(5): Show |
8 | HG01167.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+882_208+883dup others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | ||||||
| chr1:26245187 | AT | A | 29 | a0001c0001t0001g0298 a0001c0001t0002g0085 a0003c0003t0004g0017 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+883delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245187 | ||||||
| chr1:26245202 | C | T | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+884C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245202 | |||||||
| chr1:26245203 | A | C | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+885A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245203 | |||||||
| chr1:26245204 | T | A | 1 | a0001c0001t0003g0162 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.208+886T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245204 | |||||||
| chr1:26245320 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.208+1002A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245320 | |||||||
| chr1:26245360 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.208+1042C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245360 | |||||||
| chr1:26245463 | C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+1145C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245463 | |||||||
| chr1:26245484 | A | G | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.208+1166A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245484 | |||||||
| chr1:26245486 | G | A | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.208+1168G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245486 | |||||||
| chr1:26245738 | C | T | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+1420C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245738 | |||||||
| chr1:26245910 | C | A | 1 | a0002c0002t0001g0218 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.208+1592C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26245910 | |||||||
| chr1:26245979 | C | CA | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.208+1672dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26245979 | ||||||
| chr1:26246141 | A | G | 10 | a0002c0002t0001g0213 a0002c0002t0001g0214 a0002c0002t0001g0242 others(7): Show |
10 | NA18954.hp1 NA18968.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+1823A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246141 | |||||||
| chr1:26246220 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.208+1902C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246220 | |||||||
| chr1:26246301 | T | A | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.208+1983T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246301 | |||||||
| chr1:26246477 | T | C | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+2159T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246477 | |||||||
| chr1:26246532 | G | A | 28 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.208+2214G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246532 | |||||||
| chr1:26246726 | CT | C | 63 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0169 others(60): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+2411delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26246726 | ||||||
| chr1:26246728 | TTA | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0187 a0001c0001t0001g0191 others(2): Show |
6 | HG01071.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+2411_208+2412d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246728 | |||||||
| chr1:26246729 | T | A | 73 | a0001c0001t0001g0235 a0001c0001t0001g0254 a0001c0001t0001g0256 others(70): Show |
79 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.208+2411T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26246729 | |||||||
| chr1:26247150 | T | C | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+2832T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247150 | |||||||
| chr1:26247476 | T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+3158T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247476 | |||||||
| chr1:26247767 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.208+3449A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247767 | |||||||
| chr1:26247786 | C | T | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+3468C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247786 | |||||||
| chr1:26247839 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+3521G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247839 | |||||||
| chr1:26247941 | G | T | 72 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+3623G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26247941 | |||||||
| chr1:26248067 | A | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+3749A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248067 | |||||||
| chr1:26248168 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.208+3850C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248168 | |||||||
| chr1:26248175 | T | C | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3857T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248175 | |||||||
| chr1:26248176 | G | A | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3858G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248176 | |||||||
| chr1:26248177 | T | G | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.208+3859T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248177 | |||||||
| chr1:26248325 | C | A | 1 | a0001c0001t0002g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.208+4007C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248325 | |||||||
| chr1:26248478 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.208+4160T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248478 | |||||||
| chr1:26248549 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.208+4231G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248549 | |||||||
| chr1:26248677 | G | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208+4359G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248677 | |||||||
| chr1:26248722 | C | CTT | 17 | a0001c0001t0001g0177 a0001c0001t0001g0283 a0001c0001t0001g0284 others(14): Show |
17 | HG00544.hp1 HG01167.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.208+4425_208+4426d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTT | 98 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(95): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.208+4424_208+4426d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTT | 10 | a0001c0001t0001g0200 a0001c0001t0001g0205 a0002c0002t0001g0217 others(7): Show |
10 | HG00438.hp1 HG00621.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+4423_208+4426d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTT | 21 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0287 others(18): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+4422_208+4426d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTT | 8 | a0001c0001t0001g0298 a0001c0001t0003g0107 a0003c0003t0004g0290 others(5): Show |
8 | HG00323.hp2 HG00741.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+4421_208+4426d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT | 9 | a0001c0001t0003g0098 a0001c0001t0003g0104 a0001c0001t0003g0109 others(6): Show |
9 | HG02258.hp2 HG02486.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+4420_208+4426d others(9): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0117 others(4): Show |
7 | HG01891.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+4419_208+4426d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0003g0097 a0001c0001t0003g0113 a0004c0004t0003g0277 others(3): Show |
6 | HG01106.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+4418_208+4426d others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0120 others(2): Show |
7 | HG00639.hp1 HG00733.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+4417_208+4426d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0122 a0001c0001t0003g0143 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.208+4416_208+4426d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0099 a0001c0001t0003g0151 a0007c0018t0003g0123 |
3 | HG01192.hp2 HG03139.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.208+4414_208+4426d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(7): Show |
5 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0114 others(2): Show |
5 | HG00639.hp2 HG01099.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+4413_208+4426d others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.208+4412_208+4426d others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0118 a0001c0001t0003g0147 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.208+4411_208+4426d others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0003g0124 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208+4410_208+4426d others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0125 a0001c0001t0003g0135 |
2 | HG03017.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.208+4409_208+4426d others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0106 a0001c0001t0003g0110 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.208+4408_208+4426d others(21): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0003g0126 a0001c0001t0003g0152 |
2 | HG01952.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.208+4407_208+4426d others(22): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0003g0158 a0001c0001t0003g0164 |
2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.208+4406_208+4426d others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(15): Show |
6 | a0001c0001t0003g0119 a0001c0001t0003g0127 a0001c0001t0003g0128 others(3): Show |
6 | NA18943.hp2 NA18949.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+4405_208+4426d others(24): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0132 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(28): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(29): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(21): Show |
3 | a0001c0001t0003g0103 a0001c0001t0003g0134 a0001c0001t0003g0144 |
3 | HG01074.hp2 HG01358.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.208+4426_208+4427i others(30): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.208+4426_208+4427i others(32): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(36): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(33): Show |
1 | a0001c0009t0003g0108 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(42): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248722 | C | CTTTTTTT others(37): Show |
1 | a0001c0009t0003g0111 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.208+4426_208+4427i others(46): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26248722 | ||||||
| chr1:26248927 | C | T | 5 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0008g0278 others(2): Show |
5 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+4609C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248927 | |||||||
| chr1:26248990 | T | C | 1 | a0001c0001t0005g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.208+4672T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26248990 | |||||||
| chr1:26249032 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+4714A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249032 | |||||||
| chr1:26249087 | G | A | 2 | a0001c0001t0005g0026 a0001c0001t0005g0027 |
2 | HG00642.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.208+4769G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249087 | |||||||
| chr1:26249167 | C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208+4849C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249167 | |||||||
| chr1:26249186 | A | T | 1 | a0001c0001t0003g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.208+4868A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249186 | |||||||
| chr1:26249204 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.208+4886T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249204 | |||||||
| chr1:26249225 | G | A | 1 | a0004c0010t0003g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.208+4907G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249225 | |||||||
| chr1:26249238 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.208+4920C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249238 | |||||||
| chr1:26249343 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+5025A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249343 | |||||||
| chr1:26249386 | A | G | 1 | a0001c0001t0003g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.208+5068A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249386 | |||||||
| chr1:26249448 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.208+5130G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249448 | |||||||
| chr1:26249481 | C | A | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208+5163C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249481 | |||||||
| chr1:26249490 | T | C | 2 | a0001c0001t0003g0158 a0001c0001t0003g0164 |
2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.208+5172T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249490 | |||||||
| chr1:26249528 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.208+5210G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249528 | |||||||
| chr1:26249541 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.208+5223A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249541 | |||||||
| chr1:26249756 | T | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-5415T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249756 | |||||||
| chr1:26249953 | A | G | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-5218A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26249953 | |||||||
| chr1:26250165 | CAG | C | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-5003_209-5002d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250165 | ||||||
| chr1:26250775 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.209-4396T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250775 | |||||||
| chr1:26250847 | C | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-4324C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250847 | |||||||
| chr1:26250893 | A | G | 2 | a0003c0003t0004g0293 a0003c0003t0004g0300 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.209-4278A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250893 | |||||||
| chr1:26250925 | C | CCTTTTTT others(7): Show |
1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.209-4246_209-4245i others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250925 | |||||||
| chr1:26250925 | C | CT | 6 | a0001c0001t0001g0272 a0001c0001t0002g0001 a0001c0001t0002g0065 others(3): Show |
6 | HG00558.hp1 HG01891.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4240dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | C | CTT | 4 | a0001c0001t0002g0001 a0001c0001t0002g0059 a0001c0001t0002g0088 others(1): Show |
5 | HG00438.hp2 HG01192.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-4241_209-4240d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | C | CTTT | 5 | a0001c0001t0001g0271 a0001c0001t0002g0001 a0001c0001t0002g0042 others(2): Show |
5 | HG02723.hp1 NA18906.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-4242_209-4240d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(1): Show |
C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(3): Show |
6 | HG00597.hp1 HG02486.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4239_209-4232d others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(2): Show |
C | 6 | a0003c0003t0004g0299 a0003c0003t0006g0093 a0003c0003t0006g0094 others(3): Show |
6 | HG00280.hp2 HG00733.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-4239_209-4231d others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(3): Show |
C | 21 | a0001c0001t0001g0298 a0001c0016t0011g0307 a0003c0003t0004g0017 others(18): Show |
22 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-4239_209-4230d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(4): Show |
C | 5 | a0001c0001t0003g0003 a0001c0001t0003g0101 a0001c0001t0003g0120 others(2): Show |
7 | HG00733.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-4239_209-4229d others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(5): Show |
C | 64 | a0001c0001t0003g0092 a0001c0001t0003g0098 a0001c0001t0003g0099 others(61): Show |
64 | HG00544.hp1 HG00639.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.209-4239_209-4228d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(6): Show |
C | 2 | a0001c0001t0003g0107 a0001c0001t0003g0153 |
2 | HG00323.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.209-4239_209-4227d others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250925 | CTTTTTTC others(9): Show |
C | 1 | a0001c0001t0002g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.209-4239_209-4224d others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250925 | ||||||
| chr1:26250928 | T | C | 1 | a0002c0002t0007g0207 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.209-4243T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250928 | |||||||
| chr1:26250928 | TTTTC | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0187 a0001c0001t0001g0192 others(6): Show |
10 | HG00639.hp1 HG01071.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-4239_209-4236d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250928 | ||||||
| chr1:26250929 | TTTC | T | 104 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0169 others(101): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.209-4239_209-4237d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26250929 | ||||||
| chr1:26250931 | TC | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(41): Show |
54 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.209-4239delC | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250931 | |||||||
| chr1:26250932 | C | T | 42 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0002g0001 others(39): Show |
46 | HG00438.hp2 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-4239C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250932 | |||||||
| chr1:26250936 | T | C | 2 | a0001c0001t0002g0087 a0001c0001t0002g0090 |
2 | HG00621.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.209-4235T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250936 | |||||||
| chr1:26250940 | T | C | 3 | a0001c0001t0001g0177 a0002c0002t0001g0239 a0002c0002t0001g0242 |
3 | HG02280.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.209-4231T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250940 | |||||||
| chr1:26250941 | T | C | 108 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(105): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.209-4230T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250941 | |||||||
| chr1:26250942 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-4229T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26250942 | |||||||
| chr1:26251028 | G | A | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.209-4143G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251028 | |||||||
| chr1:26251091 | C | T | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-4080C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251091 | |||||||
| chr1:26251251 | G | GT | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.209-3903dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26251251 | ||||||
| chr1:26251251 | G | GTT | 18 | a0001c0001t0001g0186 a0001c0001t0001g0271 a0001c0001t0001g0272 others(15): Show |
18 | HG00639.hp1 HG01358.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-3904_209-3903d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26251251 | ||||||
| chr1:26251257 | T | TG | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-3914_209-3913i others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251257 | |||||||
| chr1:26251300 | G | A | 2 | a0002c0002t0001g0220 a0002c0002t0001g0251 |
2 | HG00280.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.209-3871G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251300 | |||||||
| chr1:26251321 | G | A | 3 | a0005c0006t0001g0247 a0005c0006t0001g0248 a0005c0006t0001g0265 |
3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.209-3850G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251321 | |||||||
| chr1:26251494 | G | A | 31 | a0001c0001t0001g0298 a0001c0001t0002g0046 a0001c0001t0002g0070 others(28): Show |
32 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.209-3677G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251494 | |||||||
| chr1:26251649 | A | G | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-3522A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251649 | |||||||
| chr1:26251742 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-3429G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251742 | |||||||
| chr1:26251852 | A | T | 1 | a0002c0002t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.209-3319A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251852 | |||||||
| chr1:26251943 | T | C | 1 | a0003c0005t0004g0282 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.209-3228T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26251943 | |||||||
| chr1:26252036 | C | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.209-3135C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252036 | |||||||
| chr1:26252123 | C | T | 1 | a0001c0001t0003g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.209-3048C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252123 | |||||||
| chr1:26252185 | C | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-2986C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252185 | |||||||
| chr1:26252251 | G | T | 5 | a0003c0003t0004g0287 a0003c0003t0004g0293 a0003c0003t0004g0294 others(2): Show |
5 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2920G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252251 | |||||||
| chr1:26252258 | G | C | 5 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0008g0278 others(2): Show |
5 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2913G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252258 | |||||||
| chr1:26252307 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.209-2864C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252307 | |||||||
| chr1:26252314 | C | T | 107 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(104): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-2857C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252314 | |||||||
| chr1:26252341 | TGACCA | T | 2 | a0001c0001t0002g0007 a0001c0001t0002g0063 |
3 | NA18968.hp1 NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.209-2828_209-2824d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26252341 | ||||||
| chr1:26252487 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.209-2684G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252487 | |||||||
| chr1:26252489 | G | A | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.209-2682G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252489 | |||||||
| chr1:26252512 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.209-2659A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252512 | |||||||
| chr1:26252732 | C | T | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.209-2439C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252732 | |||||||
| chr1:26252915 | C | T | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2256C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252915 | |||||||
| chr1:26252929 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.209-2242A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252929 | |||||||
| chr1:26252995 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.209-2176G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26252995 | |||||||
| chr1:26253070 | T | C | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.209-2101T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253070 | |||||||
| chr1:26253145 | A | G | 10 | a0001c0001t0003g0119 a0001c0001t0003g0126 a0001c0001t0003g0127 others(7): Show |
10 | HG01358.hp2 HG01952.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2026A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253145 | |||||||
| chr1:26253156 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.209-2015A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253156 | |||||||
| chr1:26253390 | C | CT | 10 | a0001c0001t0001g0177 a0001c0001t0002g0062 a0001c0001t0003g0156 others(7): Show |
10 | HG00438.hp1 HG00544.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-1764dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26253390 | ||||||
| chr1:26253390 | C | CTT | 24 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0286 others(21): Show |
25 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.209-1765_209-1764d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26253390 | ||||||
| chr1:26253590 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-1581C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253590 | |||||||
| chr1:26253683 | C | T | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1488C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253683 | |||||||
| chr1:26253685 | C | T | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1486C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253685 | |||||||
| chr1:26253688 | C | T | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1483C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253688 | |||||||
| chr1:26253689 | C | G | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1482C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253689 | |||||||
| chr1:26253690 | T | C | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1481T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253690 | |||||||
| chr1:26253692 | A | G | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1479A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253692 | |||||||
| chr1:26253694 | C | G | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1477C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253694 | |||||||
| chr1:26253695 | T | A | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1476T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253695 | |||||||
| chr1:26253697 | T | A | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1474T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253697 | |||||||
| chr1:26253698 | T | A | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1473T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253698 | |||||||
| chr1:26253699 | T | A | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1472T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253699 | |||||||
| chr1:26253705 | T | A | 1 | a0002c0002t0001g0214 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.209-1466T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253705 | |||||||
| chr1:26253839 | C | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1332C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253839 | |||||||
| chr1:26253871 | A | G | 1 | a0003c0003t0004g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.209-1300A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253871 | |||||||
| chr1:26253927 | C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.209-1244C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26253927 | |||||||
| chr1:26254299 | C | T | 12 | a0001c0001t0001g0169 a0001c0001t0001g0194 a0001c0001t0001g0195 others(9): Show |
12 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-872C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254299 | |||||||
| chr1:26254336 | T | C | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.209-835T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254336 | |||||||
| chr1:26254393 | C | T | 1 | a0002c0002t0001g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.209-778C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254393 | |||||||
| chr1:26254427 | T | TA | 30 | a0001c0001t0001g0298 a0001c0001t0002g0038 a0001c0001t0003g0158 others(27): Show |
31 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.209-731dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 26254427 | ||||||
| chr1:26254439 | A | C | 1 | a0001c0001t0002g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209-732A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254439 | |||||||
| chr1:26254446 | T | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(104): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-725T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254446 | |||||||
| chr1:26254667 | G | A | 1 | a0002c0002t0001g0269 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.209-504G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254667 | |||||||
| chr1:26254864 | T | A | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-307T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254864 | |||||||
| chr1:26254920 | A | G | 1 | a0002c0002t0001g0233 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.209-251A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 3/13 | chr1 | 26254920 | |||||||
| chr1:26256073 | A | G | 1 | a0003c0003t0004g0290 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.903+208A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256073 | |||||||
| chr1:26256195 | T | A | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.903+330T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256195 | |||||||
| chr1:26256204 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.903+339A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256204 | |||||||
| chr1:26256220 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.903+355G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256220 | |||||||
| chr1:26256222 | C | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.903+357C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256222 | |||||||
| chr1:26256335 | A | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.903+470A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256335 | |||||||
| chr1:26256596 | T | TTTTC | 4 | a0003c0003t0004g0293 a0003c0003t0004g0299 a0003c0003t0004g0300 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+735_903+738dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256596 | ||||||
| chr1:26256600 | C | CT | 6 | a0001c0001t0001g0185 a0001c0001t0001g0198 a0001c0001t0002g0044 others(3): Show |
6 | HG00438.hp2 HG02056.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+751dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256600 | ||||||
| chr1:26256600 | CTT | C | 79 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(76): Show |
81 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.903+750_903+751del others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256600 | ||||||
| chr1:26256601 | T | TTTC | 24 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(21): Show |
25 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.903+738_903+739ins others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256601 | ||||||
| chr1:26256735 | A | G | 6 | a0002c0002t0001g0015 a0002c0002t0001g0218 a0002c0002t0001g0232 others(3): Show |
7 | HG00621.hp2 HG02132.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-862A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256735 | |||||||
| chr1:26256746 | G | A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-851G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256746 | |||||||
| chr1:26256808 | C | T | 1 | a0001c0001t0003g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.904-789C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256808 | |||||||
| chr1:26256924 | T | G | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.904-673T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256924 | |||||||
| chr1:26256926 | T | G | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.904-671T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256926 | |||||||
| chr1:26256928 | G | GGGGTGTG others(3): Show |
6 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0008g0278 others(3): Show |
6 | HG00639.hp1 HG02257.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.904-668_904-667ins others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGGGTGTG others(7): Show |
2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.904-668_904-667ins others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGGGTGTG others(9): Show |
3 | a0001c0001t0012g0168 a0003c0005t0004g0282 a0003c0007t0004g0304 |
3 | HG02486.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.904-668_904-667ins others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGGGTGTG others(11): Show |
1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.904-668_904-667ins others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGGGTGTG others(13): Show |
1 | a0001c0001t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.904-668_904-667ins others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGT | 74 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(71): Show |
89 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.904-642_904-641dup others(2): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGT | 5 | a0001c0001t0002g0001 a0001c0001t0002g0052 a0001c0001t0002g0058 others(2): Show |
5 | HG01934.hp2 HG02071.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-644_904-641dup others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0003g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.904-652_904-641dup others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(7): Show |
24 | a0001c0001t0001g0298 a0001c0001t0003g0153 a0001c0001t0003g0154 others(21): Show |
24 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.904-654_904-641dup others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(9): Show |
36 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(33): Show |
36 | HG00544.hp1 HG00639.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.904-656_904-641dup others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(11): Show |
21 | a0001c0001t0003g0003 a0001c0001t0003g0098 a0001c0001t0003g0103 others(18): Show |
23 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.904-658_904-641dup others(18): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(13): Show |
5 | a0001c0001t0003g0107 a0001c0001t0003g0128 a0001c0001t0003g0129 others(2): Show |
5 | HG00323.hp2 HG02818.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-660_904-641dup others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GGTGTGTG others(15): Show |
3 | a0001c0001t0003g0097 a0001c0016t0011g0307 a0003c0003t0004g0302 |
3 | HG02683.hp2 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.904-662_904-641dup others(22): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256928 | ||||||
| chr1:26256928 | G | GTGTGTGT | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0198 |
3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.904-669_904-668ins others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(4): Show |
28 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0169 others(25): Show |
28 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(11): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(6): Show |
24 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0185 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(8): Show |
40 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0178 others(37): Show |
41 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(15): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(10): Show |
16 | a0001c0001t0001g0180 a0001c0001t0001g0284 a0002c0002t0001g0004 others(13): Show |
17 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.904-669_904-668ins others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(12): Show |
2 | a0002c0002t0001g0012 a0002c0002t0001g0209 |
2 | HG01433.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.904-669_904-668ins others(19): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(14): Show |
2 | a0001c0001t0001g0283 a0002c0002t0001g0229 |
2 | NA19079.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.904-669_904-668ins others(21): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256928 | G | GTGTGTGT others(16): Show |
1 | a0002c0002t0001g0239 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.904-669_904-668ins others(23): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256928 | |||||||
| chr1:26256930 | T | G | 1 | a0003c0007t0004g0303 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.904-667T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256930 | |||||||
| chr1:26256955 | G | GTGTGTGT others(6): Show |
1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.904-641_904-640ins others(13): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | 26256955 | ||||||
| chr1:26256956 | T | TG | 4 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0002c0002t0001g0232 others(1): Show |
4 | HG00642.hp1 HG02647.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-641_904-640ins others(1): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256956 | |||||||
| chr1:26256956 | T | TGTGTGTG others(10): Show |
5 | a0001c0001t0003g0099 a0001c0001t0003g0115 a0001c0001t0003g0136 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-641_904-640ins others(17): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256956 | |||||||
| chr1:26256981 | C | T | 1 | a0001c0001t0005g0030 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904-616C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26256981 | |||||||
| chr1:26257076 | G | A | 1 | a0001c0001t0002g0006 | 2 | NA18970.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.904-521G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257076 | |||||||
| chr1:26257087 | C | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.904-510C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257087 | |||||||
| chr1:26257122 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00642.hp1 HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.904-475G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257122 | |||||||
| chr1:26257169 | G | A | 72 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.904-428G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257169 | |||||||
| chr1:26257190 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.904-407T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257190 | |||||||
| chr1:26257213 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.904-384G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257213 | |||||||
| chr1:26257360 | A | G | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-237A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257360 | |||||||
| chr1:26257377 | A | C | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.904-220A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257377 | |||||||
| chr1:26257507 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.904-90T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257507 | |||||||
| chr1:26257564 | G | A | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-33G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 4/13 | chr1 | 26257564 | |||||||
| chr1:26257840 | G | A | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+110G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257840 | |||||||
| chr1:26257860 | T | C | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1037+130T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257860 | |||||||
| chr1:26257910 | G | A | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037+180G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26257910 | |||||||
| chr1:26258011 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1038-132C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26258011 | |||||||
| chr1:26258019 | T | C | 1 | a0002c0002t0001g0220 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1038-124T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 5/13 | chr1 | 26258019 | |||||||
| chr1:26258303 | C | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1155+43C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258303 | |||||||
| chr1:26258542 | TA | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1155+284delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 26258542 | ||||||
| chr1:26258566 | A | G | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155+306A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258566 | |||||||
| chr1:26258631 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1155+371C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258631 | |||||||
| chr1:26258640 | A | G | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0003g0003 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1155+380A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258640 | |||||||
| chr1:26258683 | G | A | 3 | a0003c0003t0006g0094 a0003c0003t0006g0095 a0003c0003t0006g0096 |
3 | HG00280.hp2 HG00733.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1155+423G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258683 | |||||||
| chr1:26258685 | C | T | 15 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(12): Show |
17 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1155+425C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258685 | |||||||
| chr1:26258752 | A | T | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1155+492A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258752 | |||||||
| chr1:26258754 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0089 |
2 | NA18940.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1155+494G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258754 | |||||||
| chr1:26258799 | G | T | 8 | a0001c0001t0003g0092 a0001c0001t0003g0105 a0001c0001t0003g0121 others(5): Show |
8 | HG03831.hp2 HG03834.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155+539G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258799 | |||||||
| chr1:26258891 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1155+631G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258891 | |||||||
| chr1:26258892 | G | C | 1 | a0001c0001t0003g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1155+632G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26258892 | |||||||
| chr1:26259166 | G | T | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1156-451G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259166 | |||||||
| chr1:26259265 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1156-352C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259265 | |||||||
| chr1:26259283 | A | G | 1 | a0002c0002t0001g0231 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1156-334A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259283 | |||||||
| chr1:26259351 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1156-266G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259351 | |||||||
| chr1:26259504 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1156-113A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259504 | |||||||
| chr1:26259590 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1156-27G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 6/13 | chr1 | 26259590 | |||||||
| chr1:26259869 | T | A | 1 | a0001c0001t0001g0298 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1341+67T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259869 | |||||||
| chr1:26259894 | G | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+92G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259894 | |||||||
| chr1:26259927 | T | A | 1 | a0004c0004t0003g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1341+125T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26259927 | |||||||
| chr1:26260112 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+310T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260112 | |||||||
| chr1:26260501 | G | GA | 110 | a0001c0001t0001g0201 a0001c0001t0001g0208 a0001c0001t0001g0298 others(107): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1341+713dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26260501 | ||||||
| chr1:26260520 | A | T | 2 | a0003c0003t0004g0288 a0003c0003t0004g0308 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1341+718A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260520 | |||||||
| chr1:26260547 | A | T | 223 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(220): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1341+745A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260547 | |||||||
| chr1:26260664 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1341+862A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26260664 | |||||||
| chr1:26261416 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1341+1614G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261416 | |||||||
| chr1:26261426 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1341+1624C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261426 | |||||||
| chr1:26261427 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+1625G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261427 | |||||||
| chr1:26261567 | T | C | 1 | a0003c0003t0006g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1341+1765T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261567 | |||||||
| chr1:26261630 | C | G | 2 | a0002c0002t0001g0230 a0002c0002t0001g0262 |
2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1341+1828C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261630 | |||||||
| chr1:26261720 | C | CTCTT | 140 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(137): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1341+1921_1341+192 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261720 | ||||||
| chr1:26261724 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1341+1922C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261724 | |||||||
| chr1:26261726 | TA | T | 6 | a0001c0001t0002g0044 a0001c0001t0002g0057 a0001c0001t0002g0063 others(3): Show |
6 | HG01975.hp2 HG02723.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1341+1939delA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261726 | ||||||
| chr1:26261727 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1341+1925A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261727 | |||||||
| chr1:26261741 | AT | A | 181 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(178): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1341+1949delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26261741 | ||||||
| chr1:26261742 | T | A | 40 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0298 others(37): Show |
41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1341+1940T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261742 | |||||||
| chr1:26261743 | T | A | 86 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0175 others(83): Show |
90 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1341+1941T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261743 | |||||||
| chr1:26261773 | T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+1971T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261773 | |||||||
| chr1:26261817 | A | C | 1 | a0004c0010t0003g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1341+2015A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26261817 | |||||||
| chr1:26262180 | G | A | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1341+2378G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262180 | |||||||
| chr1:26262239 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1341+2437G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262239 | |||||||
| chr1:26262263 | C | T | 1 | a0001c0001t0003g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1341+2461C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262263 | |||||||
| chr1:26262300 | C | G | 2 | a0002c0002t0001g0258 a0002c0002t0001g0263 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1341+2498C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262300 | |||||||
| chr1:26262306 | C | CA | 34 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(31): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1341+2513dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26262306 | ||||||
| chr1:26262335 | G | A | 72 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1341+2533G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262335 | |||||||
| chr1:26262407 | G | A | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1341+2605G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262407 | |||||||
| chr1:26262417 | G | A | 1 | a0001c0001t0005g0030 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1341+2615G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262417 | |||||||
| chr1:26262419 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1341+2617A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262419 | |||||||
| chr1:26262510 | C | T | 1 | a0001c0001t0005g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1341+2708C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262510 | |||||||
| chr1:26262535 | G | A | 1 | a0007c0018t0003g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1341+2733G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262535 | |||||||
| chr1:26262561 | G | T | 72 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1341+2759G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262561 | |||||||
| chr1:26262882 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1341+3080A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262882 | |||||||
| chr1:26262938 | T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+3136T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26262938 | |||||||
| chr1:26263145 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3343A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263145 | |||||||
| chr1:26263207 | T | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3405T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263207 | |||||||
| chr1:26263459 | A | T | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1341+3657A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263459 | |||||||
| chr1:26263496 | C | T | 1 | a0001c0001t0002g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1341+3694C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263496 | |||||||
| chr1:26263617 | G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1341+3815G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263617 | |||||||
| chr1:26263631 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00642.hp1 HG00738.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1341+3829A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263631 | |||||||
| chr1:26263691 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+3889G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263691 | |||||||
| chr1:26263753 | C | A | 1 | a0001c0001t0002g0066 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1341+3951C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263753 | |||||||
| chr1:26263807 | C | T | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341+4005C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263807 | |||||||
| chr1:26263875 | A | C | 2 | a0003c0003t0006g0094 a0003c0003t0006g0095 |
2 | HG00280.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.1341+4073A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263875 | |||||||
| chr1:26263941 | G | A | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1341+4139G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263941 | |||||||
| chr1:26263952 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1341+4150G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26263952 | |||||||
| chr1:26264110 | A | G | 71 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0098 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1341+4308A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264110 | |||||||
| chr1:26264685 | C | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1342-3798C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264685 | |||||||
| chr1:26264764 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-3719A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264764 | |||||||
| chr1:26264809 | T | A | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-3674T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264809 | |||||||
| chr1:26264979 | G | T | 1 | a0001c0001t0003g0098 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1342-3504G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26264979 | |||||||
| chr1:26264980 | C | CT | 77 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0175 others(74): Show |
80 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1342-3480dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | ||||||
| chr1:26264980 | C | CTT | 6 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0186 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342-3481_1342-348 others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | ||||||
| chr1:26264980 | CT | C | 60 | a0001c0001t0002g0048 a0001c0001t0003g0003 a0001c0001t0003g0092 others(57): Show |
62 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1342-3480delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26264980 | ||||||
| chr1:26265003 | T | TA | 5 | a0004c0004t0003g0277 a0004c0004t0003g0281 a0004c0004t0008g0278 others(2): Show |
5 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342-3479dupA | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26265003 | ||||||
| chr1:26265007 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1342-3476T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265007 | |||||||
| chr1:26265060 | T | C | 10 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0016t0011g0307 others(7): Show |
10 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1342-3423T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265060 | |||||||
| chr1:26265076 | C | T | 1 | a0004c0004t0003g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1342-3407C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265076 | |||||||
| chr1:26265145 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1342-3338G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265145 | |||||||
| chr1:26265336 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0274 |
3 | HG01081.hp1 HG01346.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1342-3147C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265336 | |||||||
| chr1:26265550 | A | G | 1 | a0002c0002t0001g0231 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1342-2933A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265550 | |||||||
| chr1:26265565 | T | C | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1342-2918T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265565 | |||||||
| chr1:26265701 | T | C | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1342-2782T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265701 | |||||||
| chr1:26265800 | C | T | 1 | a0010c0017t0004g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1342-2683C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265800 | |||||||
| chr1:26265819 | C | G | 1 | a0002c0002t0001g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1342-2664C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265819 | |||||||
| chr1:26265819 | C | T | 111 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(108): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1342-2664C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265819 | |||||||
| chr1:26265870 | C | T | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-2613C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26265870 | |||||||
| chr1:26266082 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1342-2401A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266082 | |||||||
| chr1:26266103 | G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1342-2380G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266103 | |||||||
| chr1:26266143 | A | G | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-2340A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266143 | |||||||
| chr1:26266221 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1342-2262T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266221 | |||||||
| chr1:26266223 | G | T | 29 | a0001c0001t0001g0298 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1342-2260G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266223 | |||||||
| chr1:26266236 | A | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(104): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1342-2247A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266236 | |||||||
| chr1:26266259 | A | C | 1 | a0004c0010t0003g0275 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1342-2224A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266259 | |||||||
| chr1:26266380 | C | T | 21 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(18): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1342-2103C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266380 | |||||||
| chr1:26266548 | G | A | 6 | a0001c0001t0003g0106 a0001c0001t0003g0109 a0001c0001t0003g0110 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1342-1935G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266548 | |||||||
| chr1:26266587 | T | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-1896T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266587 | |||||||
| chr1:26266591 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1342-1892A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26266591 | |||||||
| chr1:26267012 | T | C | 72 | a0001c0001t0001g0298 a0001c0001t0003g0003 a0001c0001t0003g0092 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1342-1471T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267012 | |||||||
| chr1:26267169 | G | C | 1 | a0003c0003t0004g0296 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1342-1314G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267169 | |||||||
| chr1:26267216 | TACTC | T | 3 | a0003c0003t0004g0287 a0003c0003t0004g0294 a0003c0003t0004g0302 |
3 | HG00140.hp2 HG00323.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1342-1264_1342-126 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 26267216 | ||||||
| chr1:26267273 | A | G | 2 | a0001c0001t0002g0054 a0001c0001t0002g0086 |
2 | NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1342-1210A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267273 | |||||||
| chr1:26267353 | CAG | C | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1342-1129_1342-112 others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267353 | |||||||
| chr1:26267362 | G | A | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1342-1121G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267362 | |||||||
| chr1:26267433 | G | A | 1 | a0002c0002t0010g0270 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1342-1050G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267433 | |||||||
| chr1:26267502 | C | T | 1 | a0003c0003t0004g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1342-981C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267502 | |||||||
| chr1:26267719 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0250 |
3 | NA18940.hp2 NA18966.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1342-764G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26267719 | |||||||
| chr1:26268109 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1342-374C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268109 | |||||||
| chr1:26268213 | TTTGGGAG others(3): Show |
T | 1 | a0002c0002t0001g0269 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1342-269_1342-260d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268213 | |||||||
| chr1:26268445 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1342-38G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 7/13 | chr1 | 26268445 | |||||||
| chr1:26268773 | T | C | 1 | a0002c0002t0001g0013 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1494+138T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26268773 | |||||||
| chr1:26268777 | C | T | 1 | a0002c0012t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1494+142C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26268777 | |||||||
| chr1:26269015 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1494+380C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269015 | |||||||
| chr1:26269109 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1495-351C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269109 | |||||||
| chr1:26269126 | C | T | 13 | a0001c0001t0003g0102 a0001c0001t0003g0148 a0001c0001t0003g0149 others(10): Show |
13 | HG00544.hp1 HG02056.hp2 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.1495-334C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269126 | |||||||
| chr1:26269156 | C | G | 72 | a0001c0001t0001g0298 a0001c0001t0003g0003 a0001c0001t0003g0092 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1495-304C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269156 | |||||||
| chr1:26269194 | T | C | 3 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0198 |
3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1495-266T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269194 | |||||||
| chr1:26269244 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1495-216C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269244 | |||||||
| chr1:26269342 | C | T | 3 | a0005c0006t0001g0247 a0005c0006t0001g0248 a0005c0006t0001g0265 |
3 | HG02630.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1495-118C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269342 | |||||||
| chr1:26269398 | C | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1495-62C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 8/13 | chr1 | 26269398 | |||||||
| chr1:26269782 | C | CT | 24 | a0001c0001t0001g0271 a0001c0001t0001g0284 a0001c0001t0002g0019 others(21): Show |
24 | HG00621.hp1 HG01167.hp2 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.1649+190dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | ||||||
| chr1:26269782 | C | CTT | 57 | a0001c0001t0001g0272 a0001c0001t0001g0283 a0001c0001t0002g0053 others(54): Show |
62 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1649+189_1649+190d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | ||||||
| chr1:26269782 | C | CTTT | 61 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(58): Show |
66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.1649+188_1649+190d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | ||||||
| chr1:26269782 | C | CTTTT | 17 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0184 others(14): Show |
17 | HG00741.hp1 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1649+187_1649+190d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | ||||||
| chr1:26269782 | CT | C | 10 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0136 others(7): Show |
10 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1649+190delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 26269782 | ||||||
| chr1:26269849 | C | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1649+235C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269849 | |||||||
| chr1:26269891 | A | G | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1649+277A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269891 | |||||||
| chr1:26269936 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1649+322G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269936 | |||||||
| chr1:26269978 | C | T | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1649+364C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26269978 | |||||||
| chr1:26270001 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1649+387C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270001 | |||||||
| chr1:26270027 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1649+413T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270027 | |||||||
| chr1:26270065 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0274 a0007c0018t0003g0123 |
4 | HG01081.hp1 HG01192.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1649+451C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270065 | |||||||
| chr1:26270072 | G | C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(37): Show |
43 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1649+458G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270072 | |||||||
| chr1:26270083 | G | A | 5 | a0003c0005t0004g0282 a0003c0005t0004g0305 a0003c0005t0004g0306 others(2): Show |
5 | HG02486.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1649+469G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270083 | |||||||
| chr1:26270108 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1649+494A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270108 | |||||||
| chr1:26270123 | G | A | 21 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(18): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1649+509G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270123 | |||||||
| chr1:26270218 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1649+604G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270218 | |||||||
| chr1:26270258 | G | C | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1649+644G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270258 | |||||||
| chr1:26270392 | A | C | 2 | a0002c0002t0001g0266 a0002c0002t0001g0267 |
2 | HG03834.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1650-622A>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270392 | |||||||
| chr1:26270489 | T | C | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1650-525T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270489 | |||||||
| chr1:26270586 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0171 a0001c0001t0002g0173 others(1): Show |
5 | HG02055.hp1 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650-428T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270586 | |||||||
| chr1:26270595 | C | A | 27 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(24): Show |
28 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.1650-419C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270595 | |||||||
| chr1:26270653 | G | A | 112 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(109): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1650-361G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270653 | |||||||
| chr1:26270698 | G | A | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1650-316G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270698 | |||||||
| chr1:26270944 | G | A | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1650-70G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 9/13 | chr1 | 26270944 | |||||||
| chr1:26271182 | G | A | 182 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0283 others(179): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1743+75G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271182 | |||||||
| chr1:26271290 | C | T | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1743+183C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271290 | |||||||
| chr1:26271505 | G | A | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1743+398G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271505 | |||||||
| chr1:26271550 | A | G | 78 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0298 others(75): Show |
80 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1743+443A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271550 | |||||||
| chr1:26271568 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1744-453C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271568 | |||||||
| chr1:26271616 | G | A | 1 | a0004c0004t0003g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1744-405G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271616 | |||||||
| chr1:26271624 | C | T | 1 | a0001c0016t0011g0307 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1744-397C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271624 | |||||||
| chr1:26271790 | T | C | 95 | a0001c0001t0001g0298 a0001c0001t0003g0003 a0001c0001t0003g0092 others(92): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1744-231T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271790 | |||||||
| chr1:26271877 | A | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1744-144A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26271877 | |||||||
| chr1:26272017 | T | G | 2 | a0003c0005t0004g0305 a0003c0005t0004g0306 |
2 | HG02622.hp2 HG02896.hp2 |
splice_region_variant&intron_variant | LOW | c.1744-4T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 10/13 | chr1 | 26272017 | |||||||
| chr1:26272136 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1794+65A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272136 | |||||||
| chr1:26272360 | G | T | 1 | a0002c0002t0001g0224 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1794+289G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272360 | |||||||
| chr1:26272541 | C | G | 1 | a0001c0001t0003g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1794+470C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272541 | |||||||
| chr1:26272586 | C | G | 83 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0298 others(80): Show |
85 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1794+515C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272586 | |||||||
| chr1:26272617 | A | AT | 50 | a0001c0001t0001g0177 a0001c0001t0001g0182 a0001c0001t0001g0184 others(47): Show |
50 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.1794+573dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATT | 14 | a0001c0001t0002g0040 a0001c0001t0003g0099 a0001c0001t0003g0101 others(11): Show |
14 | HG01071.hp2 HG01099.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.1794+572_1794+573d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTT | 28 | a0001c0001t0003g0003 a0001c0001t0003g0092 a0001c0001t0003g0097 others(25): Show |
30 | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1794+571_1794+573d others(5): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTT | 18 | a0001c0001t0001g0298 a0001c0001t0002g0172 a0001c0001t0003g0098 others(15): Show |
18 | HG00323.hp2 HG00544.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1794+570_1794+573d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTTT | 6 | a0001c0001t0003g0114 a0001c0001t0003g0119 a0001c0001t0003g0126 others(3): Show |
6 | HG01358.hp2 HG01952.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1794+569_1794+573d others(7): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTTTT | 11 | a0001c0001t0003g0104 a0001c0001t0003g0127 a0001c0001t0003g0128 others(8): Show |
11 | HG02293.hp2 HG03516.hp1 NA18906.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+568_1794+573d others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTTTTT others(3): Show |
1 | a0004c0004t0003g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1794+564_1794+573d others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1794+562_1794+573d others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | A | ATTTTTTT others(29): Show |
1 | a0001c0001t0001g0272 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1794+573_1794+574i others(38): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272617 | AT | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0283 a0001c0001t0001g0284 others(8): Show |
11 | HG01167.hp2 HG01515.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+573delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26272617 | ||||||
| chr1:26272641 | T | G | 2 | a0003c0007t0004g0303 a0003c0007t0004g0304 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1794+570T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272641 | |||||||
| chr1:26272642 | T | G | 23 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(20): Show |
24 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1794+571T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272642 | |||||||
| chr1:26272642 | T | TG | 3 | a0003c0003t0004g0301 a0003c0003t0006g0096 a0010c0017t0004g0289 |
3 | HG01361.hp1 HG02572.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1794+571_1794+572i others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272642 | |||||||
| chr1:26272645 | G | T | 26 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(23): Show |
27 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1794+574G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272645 | |||||||
| chr1:26272668 | G | A | 2 | a0003c0008t0004g0291 a0003c0008t0004g0292 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1794+597G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272668 | |||||||
| chr1:26272697 | C | T | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1794+626C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272697 | |||||||
| chr1:26272769 | C | T | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1794+698C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272769 | |||||||
| chr1:26272778 | A | G | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1794+707A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272778 | |||||||
| chr1:26272790 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1794+719G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272790 | |||||||
| chr1:26272817 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1794+746C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272817 | |||||||
| chr1:26272881 | G | A | 1 | a0003c0003t0004g0302 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1794+810G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272881 | |||||||
| chr1:26272998 | A | G | 71 | a0001c0001t0001g0298 a0001c0001t0003g0003 a0001c0001t0003g0092 others(68): Show |
73 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1794+927A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26272998 | |||||||
| chr1:26273044 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1794+973G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273044 | |||||||
| chr1:26273051 | G | A | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1794+980G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273051 | |||||||
| chr1:26273097 | G | C | 1 | a0002c0002t0007g0207 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1026G>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273097 | |||||||
| chr1:26273098 | A | G | 1 | a0002c0002t0007g0207 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1027A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273098 | |||||||
| chr1:26273099 | G | A | 1 | a0002c0002t0007g0207 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1794+1028G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273099 | |||||||
| chr1:26273105 | A | G | 2 | a0002c0002t0001g0258 a0002c0002t0001g0263 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1794+1034A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273105 | |||||||
| chr1:26273258 | G | A | 3 | a0003c0003t0004g0285 a0003c0003t0004g0286 a0003c0003t0004g0296 |
3 | HG02896.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1794+1187G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273258 | |||||||
| chr1:26273317 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1794+1246G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273317 | |||||||
| chr1:26273350 | C | T | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1794+1279C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273350 | |||||||
| chr1:26273724 | G | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1795-1240G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273724 | |||||||
| chr1:26273813 | T | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(221): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1795-1151T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273813 | |||||||
| chr1:26273846 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1795-1118G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273846 | |||||||
| chr1:26273900 | C | CTAAA | 66 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0169 others(63): Show |
71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | |||||||
| chr1:26273900 | C | CTAAATAA others(1): Show |
41 | a0001c0001t0001g0010 a0001c0001t0001g0178 a0001c0001t0001g0179 others(38): Show |
45 | HG00140.hp1 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | |||||||
| chr1:26273900 | C | CTAAATAA others(5): Show |
3 | a0001c0001t0001g0272 a0005c0006t0001g0248 a0005c0006t0001g0265 |
3 | HG01891.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1795-1064_1795-106 others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | |||||||
| chr1:26273900 | C | CTAAATAA others(9): Show |
1 | a0002c0002t0001g0219 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1795-1064_1795-106 others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273900 | |||||||
| chr1:26273901 | A | AAAAT | 9 | a0001c0001t0002g0039 a0001c0001t0002g0046 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1795-1035_1795-103 others(8): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | ||||||
| chr1:26273901 | A | AAAATAAA others(1): Show |
54 | a0001c0001t0003g0003 a0001c0001t0003g0099 a0001c0001t0003g0100 others(51): Show |
56 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1795-1039_1795-103 others(12): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | ||||||
| chr1:26273901 | A | AAAATAAA others(5): Show |
11 | a0001c0001t0001g0298 a0001c0001t0003g0098 a0001c0001t0003g0136 others(8): Show |
11 | HG01358.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1795-1043_1795-103 others(16): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | ||||||
| chr1:26273901 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0154 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1795-1047_1795-103 others(20): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273901 | ||||||
| chr1:26273901 | A | T | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1795-1063A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273901 | |||||||
| chr1:26273931 | A | AATAAAT | 5 | a0003c0003t0004g0295 a0003c0003t0004g0299 a0003c0005t0004g0282 others(2): Show |
5 | HG00741.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(10): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273931 | ||||||
| chr1:26273931 | A | AATAAATA others(3): Show |
21 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(18): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26273931 | ||||||
| chr1:26273932 | A | ATAAATAA others(3): Show |
5 | a0001c0001t0003g0092 a0001c0001t0003g0121 a0001c0001t0003g0124 others(2): Show |
5 | NA18952.hp2 NA18970.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-1032_1795-103 others(14): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273932 | |||||||
| chr1:26273934 | T | A | 29 | a0001c0001t0003g0097 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1795-1030T>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273934 | |||||||
| chr1:26273992 | A | G | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1795-972A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26273992 | |||||||
| chr1:26274023 | GT | G | 219 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(216): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1795-930delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274023 | ||||||
| chr1:26274192 | CACTT | C | 21 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(18): Show |
22 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1795-769_1795-766d others(6): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274192 | ||||||
| chr1:26274200 | C | T | 1 | a0002c0002t0001g0273 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1795-764C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274200 | |||||||
| chr1:26274250 | A | AT | 3 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 |
3 | NA18986.hp2 NA19068.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1795-713dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 26274250 | ||||||
| chr1:26274302 | A | G | 108 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(105): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1795-662A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274302 | |||||||
| chr1:26274667 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1795-297G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274667 | |||||||
| chr1:26274882 | T | C | 4 | a0004c0004t0003g0277 a0004c0004t0008g0278 a0004c0004t0008g0279 others(1): Show |
4 | HG00639.hp1 HG02257.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-82T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274882 | |||||||
| chr1:26274892 | C | T | 3 | a0001c0001t0003g0128 a0001c0001t0003g0158 a0001c0001t0003g0164 |
3 | NA18986.hp1 NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1795-72C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274892 | |||||||
| chr1:26274894 | G | A | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1795-70G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 11/13 | chr1 | 26274894 | |||||||
| chr1:26275079 | A | G | 29 | a0001c0001t0002g0039 a0003c0003t0004g0017 a0003c0003t0004g0285 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1902+8A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275079 | |||||||
| chr1:26275186 | A | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1902+115A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275186 | |||||||
| chr1:26275264 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1902+193A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275264 | |||||||
| chr1:26275283 | G | GT | 72 | a0001c0001t0001g0208 a0001c0001t0001g0298 a0001c0001t0002g0045 others(69): Show |
74 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1902+228dupT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275283 | ||||||
| chr1:26275283 | GT | G | 6 | a0001c0001t0001g0178 a0001c0001t0002g0058 a0001c0001t0002g0077 others(3): Show |
6 | HG01515.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1902+228delT | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275283 | ||||||
| chr1:26275404 | C | CTG | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0004c0004t0003g0277 others(6): Show |
9 | HG00639.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1902+337_1902+338d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 26275404 | ||||||
| chr1:26275467 | G | A | 7 | a0004c0004t0003g0277 a0004c0004t0003g0280 a0004c0004t0003g0281 others(4): Show |
7 | HG00639.hp1 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1902+396G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275467 | |||||||
| chr1:26275760 | C | T | 113 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(110): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1902+689C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275760 | |||||||
| chr1:26275765 | T | G | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1902+694T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275765 | |||||||
| chr1:26275805 | C | G | 1 | a0002c0002t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1903-730C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275805 | |||||||
| chr1:26275816 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1903-719G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275816 | |||||||
| chr1:26275820 | G | T | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-715G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275820 | |||||||
| chr1:26275821 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-714G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275821 | |||||||
| chr1:26275822 | A | T | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-713A>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275822 | |||||||
| chr1:26275823 | C | A | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-712C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275823 | |||||||
| chr1:26275824 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-711T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275824 | |||||||
| chr1:26275825 | C | A | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-710C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275825 | |||||||
| chr1:26275828 | T | G | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-707T>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275828 | |||||||
| chr1:26275830 | C | G | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-705C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275830 | |||||||
| chr1:26275832 | G | T | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-703G>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275832 | |||||||
| chr1:26275833 | A | G | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-702A>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275833 | |||||||
| chr1:26275834 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1903-701C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275834 | |||||||
| chr1:26275867 | G | A | 1 | a0003c0003t0004g0301 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1903-668G>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26275867 | |||||||
| chr1:26276019 | C | T | 2 | a0001c0001t0003g0150 a0001c0001t0003g0156 |
2 | HG00544.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1903-516C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276019 | |||||||
| chr1:26276023 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1903-512C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276023 | |||||||
| chr1:26276034 | C | T | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1903-501C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276034 | |||||||
| chr1:26276037 | C | A | 1 | a0001c0001t0003g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1903-498C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276037 | |||||||
| chr1:26276059 | T | C | 31 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0002c0002t0001g0005 others(28): Show |
34 | HG00621.hp2 HG01261.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.1903-476T>C | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276059 | |||||||
| chr1:26276065 | C | G | 38 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(35): Show |
41 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1903-470C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276065 | |||||||
| chr1:26276076 | TGA | T | 28 | a0003c0003t0004g0017 a0003c0003t0004g0285 a0003c0003t0004g0286 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1903-458_1903-457d others(4): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276076 | |||||||
| chr1:26276328 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1903-207C>T | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276328 | |||||||
| chr1:26276494 | C | G | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1903-41C>G | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 12/13 | chr1 | 26276494 | |||||||
| chr1:26276800 | CCTT | C | 5 | a0003c0003t0004g0287 a0003c0003t0004g0293 a0003c0003t0004g0294 others(2): Show |
5 | HG00140.hp2 HG00323.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2128+44_2128+46del others(3): Show |
CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 26276800 | ||||||
| chr1:26276957 | C | A | 1 | a0001c0001t0012g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2129-179C>A | CEP85 | ENSG00000130695.16 | transcript | ENST00000451429.8 | protein_coding | 13/13 | chr1 | 26276957 |