Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9662 |
| ensemblid | ENSG00000174799.12 |
| hgncid | 29086 |
| symbol | CEP135 |
| name | centrosomal protein 135 |
| refseq_nuc | NM_025009.5 |
| refseq_prot | NP_079285.2 |
| ensembl_nuc | ENST00000257287.5 |
| ensembl_prot | ENSP00000257287.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 55948945 |
| end | 56033361 |
| strand | + |
| ver | v1.2 |
| region | chr4:55948945-56033361 |
| region5000 | chr4:55943945-56038361 |
| regionname0 | CEP135_chr4_55948945_56033361 |
| regionname5000 | CEP135_chr4_55943945_56038361 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1140 | 274 | 59 | 55 | 119 | 12 | 27 | 101 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0002 | 0/0 | 1140 | 48 | 7 | 10 | 23 | 2 | 6 | 20 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0003 | 0/0 | 1140 | 5 | 0 | 2 | 0 | 2 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0004 | 0/0 | 1140 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0005 | 0/0 | 1140 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0006 | 0/0 | 1140 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0007 | 0/0 | 1140 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0008 | 0/0 | 1140 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0009 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0010 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0011 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0012 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | MTTAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| a0013 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | MATAV others(1135): Show |
chr4 | 55943945 | 56038361 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3420 | 257 | 56 | 44 | 117 | 12 | 26 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0001c0003 | 0/0 | 3420 | 11 | 2 | 7 | 1 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0001c0007 | 0/0 | 3420 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0001c0013 | 0/0 | 3420 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0001c0015 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0001c0016 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0002c0002 | 0/0 | 3420 | 48 | 7 | 10 | 23 | 2 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0003c0004 | 0/0 | 3420 | 5 | 0 | 2 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0004c0005 | 0/0 | 3420 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0005c0006 | 0/0 | 3420 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0006c0008 | 0/0 | 3420 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0007c0009 | 0/0 | 3420 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0008c0010 | 0/0 | 3420 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0009c0014 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0010c0011 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0011c0012 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0012c0017 | 0/0 | 3420 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGAC others(3415): Show |
chr4 | 55943945 | 56038361 | ||
| a0013c0018 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATGGC others(3415): Show |
chr4 | 55943945 | 56038361 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5596 | 80 | 13 | 9 | 48 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0002 | 0/0 | 5605 | 76 | 3 | 9 | 51 | 3 | 10 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0003 | 0/0 | 5597 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0004 | 0/0 | 5605 | 31 | 8 | 10 | 10 | 1 | 2 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0005 | 0/1 | 5596 | 22 | 7 | 4 | 1 | 3 | 6 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0006 | 0/0 | 5595 | 10 | 3 | 4 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5590): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0007 | 0/0 | 5599 | 5 | 5 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5594): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0009 | 0/0 | 5598 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5593): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0010 | 0/0 | 5607 | 4 | 2 | 1 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5602): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0011 | 0/0 | 5603 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5598): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0012 | 0/0 | 5598 | 4 | 3 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5593): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0013 | 0/0 | 5603 | 3 | 2 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5598): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0014 | 0/0 | 5603 | 2 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5598): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0016 | 0/0 | 5596 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0019 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0020 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5590): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0021 | 0/0 | 5606 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5601): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0022 | 0/0 | 5606 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5601): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0023 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5590): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0024 | 0/0 | 5607 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5602): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0025 | 0/0 | 5607 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5602): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0026 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0028 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0029 | 0/0 | 5596 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0030 | 0/0 | 5596 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0001t0031 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5590): Show |
chr4 | 55943945 | 56038361 |
| a0001c0003t0003 | 0/0 | 5597 | 11 | 2 | 7 | 1 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0001c0007t0001 | 0/0 | 5596 | 3 | 0 | 3 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0013t0005 | 0/0 | 5596 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0001c0015t0004 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0001c0016t0027 | 0/0 | 5605 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0002c0002t0003 | 0/0 | 5597 | 41 | 6 | 9 | 19 | 2 | 5 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0002c0002t0004 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0002c0002t0006 | 0/0 | 5595 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5590): Show |
chr4 | 55943945 | 56038361 |
| a0002c0002t0015 | 0/0 | 5599 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5594): Show |
chr4 | 55943945 | 56038361 |
| a0002c0002t0017 | 0/0 | 5597 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0003c0004t0003 | 0/0 | 5597 | 5 | 0 | 2 | 0 | 2 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0004c0005t0001 | 0/0 | 5596 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0005c0006t0008 | 0/0 | 5600 | 4 | 4 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5595): Show |
chr4 | 55943945 | 56038361 |
| a0006c0008t0011 | 0/0 | 5603 | 2 | 1 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5598): Show |
chr4 | 55943945 | 56038361 |
| a0007c0009t0002 | 0/0 | 5605 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0008c0010t0001 | 0/0 | 5596 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0009c0014t0002 | 0/0 | 5605 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5600): Show |
chr4 | 55943945 | 56038361 |
| a0010c0011t0005 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| a0011c0012t0008 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5595): Show |
chr4 | 55943945 | 56038361 |
| a0012c0017t0003 | 0/0 | 5597 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5592): Show |
chr4 | 55943945 | 56038361 |
| a0013c0018t0018 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | ATTTT others(5591): Show |
chr4 | 55943945 | 56038361 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 5 | 0 | 1 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0007g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0010g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0012g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0013g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0014g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0016g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0020g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0022g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0023g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0024g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0025g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0026g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0028g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0029g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0030g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0001t0031g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0003 | 0/0 | 5 | 1 | 3 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0007t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0007t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0013t0005g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0015t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0001c0016t0027g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0002 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0015g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0002c0002t0017g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0003c0004t0003g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0003c0004t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0003c0004t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0004c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0004c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0004c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0004c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0005c0006t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0005c0006t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0005c0006t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0005c0006t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0006c0008t0011g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0006c0008t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0007c0009t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0007c0009t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0008c0010t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0008c0010t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0009c0014t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0010c0011t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0011c0012t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0012c0017t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| a0013c0018t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | GBR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0018 | EUR | GBR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0050 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0046 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0247 | EUR | FIN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00408 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00558 | hp2 | a0001 | c0003 | t0003 | g0003 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00639 | hp1 | a0001 | c0001 | t0025 | g0008 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00639 | hp2 | a0002 | c0002 | t0003 | g0138 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00673 | hp2 | a0009 | c0014 | t0002 | g0096 | EAS | CHS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00733 | hp2 | a0003 | c0004 | t0003 | g0139 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0307 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00738 | hp2 | a0003 | c0004 | t0003 | g0007 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0272 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01070 | hp1 | a0001 | c0007 | t0001 | g0017 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0271 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01071 | hp2 | a0001 | c0007 | t0001 | g0017 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01099 | hp1 | a0001 | c0013 | t0005 | g0187 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01099 | hp2 | a0002 | c0002 | t0015 | g0162 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0130 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01167 | hp1 | a0001 | c0007 | t0001 | g0226 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0158 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0161 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0160 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01243 | hp2 | a0006 | c0008 | t0011 | g0029 | AMR | PUR | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01255 | hp1 | a0001 | c0001 | t0030 | g0151 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0150 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0211 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01257 | hp2 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01258 | hp2 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0020 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0146 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01358 | hp2 | a0007 | c0009 | t0002 | g0094 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01361 | hp1 | a0007 | c0009 | t0002 | g0114 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01433 | hp2 | a0002 | c0002 | t0003 | g0261 | AMR | CLM | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01515 | hp1 | a0002 | c0002 | t0003 | g0136 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0252 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0002 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0065 | EUR | IBS | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0263 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01928 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01928 | hp2 | a0001 | c0001 | t0023 | g0116 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0048 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0244 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG01993 | hp2 | a0001 | c0003 | t0003 | g0274 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02004 | hp2 | a0001 | c0001 | t0013 | g0008 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0128 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0127 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0304 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0010 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0134 | EAS | CDX | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | CDX | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0266 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0027 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0305 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0273 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02523 | hp1 | a0001 | c0001 | t0022 | g0115 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0153 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02572 | hp2 | a0001 | c0001 | t0009 | g0197 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02622 | hp2 | a0004 | c0005 | t0001 | g0178 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0278 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0299 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0002 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02886 | hp1 | a0010 | c0011 | t0005 | g0163 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0156 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02970 | hp2 | a0001 | c0016 | t0027 | g0276 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0034 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02976 | hp2 | a0005 | c0006 | t0008 | g0159 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03017 | hp1 | a0001 | c0003 | t0003 | g0020 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03017 | hp2 | a0002 | c0002 | t0003 | g0149 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03130 | hp2 | a0004 | c0005 | t0001 | g0215 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0133 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03139 | hp2 | a0004 | c0005 | t0001 | g0239 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0147 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0246 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03486 | hp1 | a0005 | c0006 | t0008 | g0155 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03486 | hp2 | a0011 | c0012 | t0008 | g0179 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03492 | hp1 | a0002 | c0002 | t0017 | g0306 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0286 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0218 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0049 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0242 | SAS | PJL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03834 | hp2 | a0003 | c0004 | t0003 | g0141 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0210 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0180 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04115 | hp2 | a0002 | c0002 | t0003 | g0126 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0175 | SAS | BEB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0233 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18522 | hp1 | a0006 | c0008 | t0011 | g0030 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18940 | hp2 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18948 | hp2 | a0002 | c0002 | t0006 | g0140 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0132 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18952 | hp2 | a0002 | c0002 | t0003 | g0145 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18968 | hp1 | a0002 | c0002 | t0006 | g0148 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0062 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18975 | hp1 | a0002 | c0002 | t0003 | g0135 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18979 | hp2 | a0001 | c0001 | t0026 | g0255 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18983 | hp2 | a0001 | c0015 | t0004 | g0284 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18986 | hp1 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18988 | hp1 | a0012 | c0017 | t0003 | g0002 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18989 | hp1 | a0008 | c0010 | t0001 | g0229 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0137 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18995 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18995 | hp2 | a0008 | c0010 | t0001 | g0232 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19006 | hp1 | a0001 | c0001 | t0010 | g0105 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0142 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19010 | hp1 | a0002 | c0002 | t0003 | g0144 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0288 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0043 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19057 | hp1 | a0001 | c0001 | t0028 | g0176 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0089 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19058 | hp1 | a0001 | c0001 | t0029 | g0191 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0118 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19079 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19081 | hp1 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19084 | hp1 | a0002 | c0002 | t0003 | g0308 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19090 | hp1 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0268 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA19240 | hp2 | a0013 | c0018 | t0018 | g0269 | AFR | YRI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | ASW | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20129 | hp2 | a0005 | c0006 | t0008 | g0152 | AFR | ASW | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20752 | hp2 | a0003 | c0004 | t0003 | g0007 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0303 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20805 | hp2 | a0003 | c0004 | t0003 | g0007 | EUR | TSI | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | GIH | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0035 | SAS | GIH | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02109 | hp1 | a0001 | c0001 | t0031 | g0129 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03471 | hp1 | a0002 | c0002 | t0015 | g0014 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | MSL | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG06807 | hp1 | a0001 | c0001 | t0021 | g0122 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA20300 | hp2 | a0004 | c0005 | t0001 | g0240 | AFR | USA | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0267 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| NA21309 | hp2 | a0005 | c0006 | t0008 | g0157 | AFR | LWK | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0237 | REF | REF | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CEP135_chr4_55943945_56038361 | CEP135 | chr4 | 55943945 | 56038361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55952134 | A | G | 1 | a0013 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.4A>G | p.Thr2Ala | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/26 | 164/5596 | 4/3423 | 2/1140 | chr4 | 55952134 | |||
| chr4:55954246 | G | A | 1 | a0003 | 5 | HG00733.hp2 HG00738.hp2 HG03834.hp2 others(2): Show |
missense_variant | MODERATE | c.335G>A | p.Arg112His | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/26 | 495/5596 | 335/3423 | 112/1140 | chr4 | 55954246 | |||
| chr4:55959687 | A | C | 1 | a0012 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.620A>C | p.Gln207Pro | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/26 | 780/5596 | 620/3423 | 207/1140 | chr4 | 55959687 | |||
| chr4:55959753 | A | G | 1 | a0008 | 2 | NA18989.hp1 NA18995.hp2 |
missense_variant | MODERATE | c.686A>G | p.Asp229Gly | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/26 | 846/5596 | 686/3423 | 229/1140 | chr4 | 55959753 | |||
| chr4:55965752 | G | A | 1 | a0010 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.937G>A | p.Glu313Lys | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/26 | 1097/5596 | 937/3423 | 313/1140 | chr4 | 55965752 | |||
| chr4:55971379 | G | A | 2 | a0004 a0011 |
5 | HG02622.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.1220G>A | p.Ser407Asn | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/26 | 1380/5596 | 1220/3423 | 407/1140 | chr4 | 55971379 | |||
| chr4:55974909 | A | T | 1 | a0009 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1413A>T | p.Arg471Ser | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1573/5596 | 1413/3423 | 471/1140 | chr4 | 55974909 | |||
| chr4:55981275 | G | A | 1 | a0005 | 4 | HG02976.hp2 HG03486.hp1 NA20129.hp2 others(1): Show |
missense_variant | MODERATE | c.1675G>A | p.Ala559Thr | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/26 | 1835/5596 | 1675/3423 | 559/1140 | chr4 | 55981275 | |||
| chr4:56008351 | A | C | 3 | a0002 a0003 a0012 |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
missense_variant | MODERATE | c.2305A>C | p.Ile769Leu | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/26 | 2465/5596 | 2305/3423 | 769/1140 | chr4 | 56008351 | |||
| chr4:56009796 | G | C | 1 | a0011 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2398G>C | p.Asp800His | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/26 | 2558/5596 | 2398/3423 | 800/1140 | chr4 | 56009796 | |||
| chr4:56020725 | T | A | 1 | a0006 | 2 | HG01243.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.3265T>A | p.Leu1089Ile | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/26 | 3425/5596 | 3265/3423 | 1089/1140 | chr4 | 56020725 | |||
| chr4:56024527 | G | A | 1 | a0007 | 2 | HG01358.hp2 HG01361.hp1 |
missense_variant | MODERATE | c.3347G>A | p.Arg1116Gln | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/26 | 3507/5596 | 3347/3423 | 1116/1140 | chr4 | 56024527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55974750 | A | G | 1 | a0001c0016 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1254A>G | p.Arg418Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1414/5596 | 1254/3423 | 418/1140 | chr4 | 55974750 | |||
| chr4:55974855 | A | G | 1 | a0001c0015 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1359A>G | p.Glu453Glu | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/26 | 1519/5596 | 1359/3423 | 453/1140 | chr4 | 55974855 | |||
| chr4:55981340 | A | G | 1 | a0001c0013 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.1740A>G | p.Arg580Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/26 | 1900/5596 | 1740/3423 | 580/1140 | chr4 | 55981340 | |||
| chr4:56011907 | A | G | 1 | a0010c0011 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2724A>G | p.Arg908Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/26 | 2884/5596 | 2724/3423 | 908/1140 | chr4 | 56011907 | |||
| chr4:56011938 | A | C | 1 | a0001c0007 | 3 | HG01070.hp1 HG01071.hp2 HG01167.hp1 |
synonymous_variant | LOW | c.2755A>C | p.Arg919Arg | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/26 | 2915/5596 | 2755/3423 | 919/1140 | chr4 | 56011938 | |||
| chr4:56017821 | C | G | 1 | a0001c0003 | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
synonymous_variant | LOW | c.2976C>G | p.Thr992Thr | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/26 | 3136/5596 | 2976/3423 | 992/1140 | chr4 | 56017821 | |||
| chr4:56019415 | T | C | 1 | a0001c0003 | 11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
synonymous_variant | LOW | c.3075T>C | p.Asn1025Asn | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/26 | 3235/5596 | 3075/3423 | 1025/1140 | chr4 | 56019415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55948964 | G | T | 1 | a0001c0001t0031 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-141G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/26 | 3167 | chr4 | 55948964 | ||||||
| chr4:55948979 | T | C | 6 | a0001c0001t0005 a0001c0001t0016 a0001c0013t0005 others(3): Show |
26 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-126T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/26 | 3152 | chr4 | 55948979 | ||||||
| chr4:56031397 | A | C | 4 | a0001c0001t0012 a0001c0001t0030 a0005c0006t0008 others(1): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 6794 | chr4 | 56031397 | ||||||
| chr4:56031562 | C | T | 3 | a0001c0001t0007 a0001c0001t0011 a0006c0008t0011 |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*214C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 6959 | chr4 | 56031562 | ||||||
| chr4:56031851 | T | C | 4 | a0001c0001t0012 a0001c0001t0030 a0005c0006t0008 others(1): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*503T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7248 | chr4 | 56031851 | ||||||
| chr4:56031856 | G | C | 1 | a0001c0001t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7253 | chr4 | 56031856 | ||||||
| chr4:56032046 | A | G | 1 | a0001c0001t0029 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*698A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7443 | chr4 | 56032046 | ||||||
| chr4:56032050 | A | G | 1 | a0001c0001t0028 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*702A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7447 | chr4 | 56032050 | ||||||
| chr4:56032074 | A | G | 1 | a0001c0016t0027 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*726A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7471 | chr4 | 56032074 | ||||||
| chr4:56032167 | G | A | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7564 | chr4 | 56032167 | ||||||
| chr4:56032173 | A | G | 1 | a0001c0001t0026 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7570 | chr4 | 56032173 | ||||||
| chr4:56032218 | G | A | 1 | a0001c0001t0021 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*870G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7615 | chr4 | 56032218 | ||||||
| chr4:56032248 | C | G | 1 | a0013c0018t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*900C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7645 | chr4 | 56032248 | ||||||
| chr4:56032288 | T | C | 1 | a0001c0001t0016 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*940T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7685 | chr4 | 56032288 | ||||||
| chr4:56032446 | GA | G | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(25): Show |
212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1111delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7856 | INFO_REALIGN_3_PRIME | chr4 | 56032446 | |||||
| chr4:56032470 | T | A | 2 | a0001c0001t0014 a0001c0016t0027 |
3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1122T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 7867 | chr4 | 56032470 | ||||||
| chr4:56032628 | T | G | 3 | a0001c0001t0007 a0001c0001t0011 a0006c0008t0011 |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1280T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8025 | chr4 | 56032628 | ||||||
| chr4:56032847 | A | AGT | 8 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(5): Show |
68 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1522_*1523dupGT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | |||||
| chr4:56032847 | A | AGTGT | 4 | a0001c0001t0007 a0002c0002t0015 a0005c0006t0008 others(1): Show |
12 | HG01099.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1520_*1523dupGTGT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | |||||
| chr4:56032847 | A | AGTGTGTG others(1): Show |
4 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0014 others(1): Show |
9 | HG01243.hp2 HG02004.hp2 HG02300.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1516_*1523dupGTGT others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | |||||
| chr4:56032847 | A | AGTGTGTG others(3): Show |
10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0019 others(7): Show |
116 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1523dupGTGT others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | |||||
| chr4:56032847 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0010 a0001c0001t0024 a0001c0001t0025 |
6 | HG00639.hp1 HG02148.hp2 HG02451.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1512_*1523dupGTGT others(8): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8269 | INFO_REALIGN_3_PRIME | chr4 | 56032847 | |||||
| chr4:56032848 | G | A | 1 | a0001c0001t0020 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1500G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8245 | chr4 | 56032848 | ||||||
| chr4:56033078 | C | A | 1 | a0001c0001t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8475 | chr4 | 56033078 | ||||||
| chr4:56033211 | A | G | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0022 others(3): Show |
85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1863A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 26/26 | 8608 | chr4 | 56033211 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55949238 | C | T | 1 | a0002c0002t0003g0308 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-46+179C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949238 | |||||||
| chr4:55949253 | C | G | 1 | a0001c0001t0005g0307 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-46+194C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949253 | |||||||
| chr4:55949273 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-46+214G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949273 | |||||||
| chr4:55949331 | C | G | 1 | a0002c0002t0017g0306 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46+272C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949331 | |||||||
| chr4:55949332 | G | T | 1 | a0002c0002t0017g0306 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-46+273G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949332 | |||||||
| chr4:55949714 | C | T | 33 | a0001c0001t0001g0294 a0001c0001t0002g0282 a0001c0001t0004g0008 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46+655C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949714 | |||||||
| chr4:55949765 | T | A | 1 | a0001c0001t0005g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-46+706T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55949765 | |||||||
| chr4:55950000 | A | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-46+941A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950000 | |||||||
| chr4:55950091 | GTCTC | G | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1034_-46+1037d others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950091 | ||||||
| chr4:55950096 | T | A | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1037T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950096 | |||||||
| chr4:55950331 | G | C | 1 | a0001c0001t0002g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-46+1272G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950331 | |||||||
| chr4:55950378 | T | G | 1 | a0001c0001t0006g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-46+1319T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950378 | |||||||
| chr4:55950423 | G | C | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-46+1364G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950423 | |||||||
| chr4:55950640 | T | TA | 6 | a0001c0001t0004g0008 a0001c0001t0004g0279 a0001c0001t0004g0280 others(3): Show |
6 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-1434dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950640 | ||||||
| chr4:55950679 | T | C | 1 | a0001c0001t0004g0281 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-45-1407T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950679 | |||||||
| chr4:55950723 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-45-1363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55950723 | |||||||
| chr4:55950759 | C | CT | 33 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-45-1318dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950759 | ||||||
| chr4:55950798 | C | CAT | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-45-1286_-45-1285d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr4 | 55950798 | ||||||
| chr4:55951534 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-45-552G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951534 | |||||||
| chr4:55951698 | C | G | 1 | a0001c0001t0002g0270 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-45-388C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951698 | |||||||
| chr4:55951828 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
3 | NA18955.hp1 NA19011.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-45-258G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55951828 | |||||||
| chr4:55952021 | C | T | 1 | a0013c0018t0018g0269 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-45-65C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 1/25 | chr4 | 55952021 | |||||||
| chr4:55952335 | A | G | 1 | a0001c0001t0024g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.113+92A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952335 | |||||||
| chr4:55952545 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.113+302T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952545 | |||||||
| chr4:55952546 | C | T | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.113+303C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952546 | |||||||
| chr4:55952654 | G | A | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.113+411G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952654 | |||||||
| chr4:55952682 | C | T | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.114-403C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952682 | |||||||
| chr4:55952875 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA18948.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.114-210A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 2/25 | chr4 | 55952875 | |||||||
| chr4:55953514 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.304+239G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953514 | |||||||
| chr4:55953570 | T | C | 1 | a0002c0002t0003g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.304+295T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953570 | |||||||
| chr4:55953943 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305-273C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55953943 | |||||||
| chr4:55954045 | T | G | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-171T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954045 | |||||||
| chr4:55954064 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.305-152T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954064 | |||||||
| chr4:55954136 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.305-80T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 3/25 | chr4 | 55954136 | |||||||
| chr4:55954401 | C | T | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.472+18C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954401 | |||||||
| chr4:55954550 | G | C | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.472+167G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954550 | |||||||
| chr4:55954566 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472+183G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954566 | |||||||
| chr4:55954604 | A | G | 8 | a0001c0001t0006g0032 a0001c0001t0006g0044 a0001c0001t0006g0045 others(5): Show |
8 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+221A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954604 | |||||||
| chr4:55954923 | A | T | 1 | a0002c0002t0003g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+540A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954923 | |||||||
| chr4:55954924 | T | A | 1 | a0002c0002t0003g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+541T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954924 | |||||||
| chr4:55954926 | C | A | 1 | a0002c0002t0003g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+543C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954926 | |||||||
| chr4:55954927 | A | C | 1 | a0002c0002t0003g0262 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.472+544A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954927 | |||||||
| chr4:55954970 | A | T | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.472+587A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55954970 | |||||||
| chr4:55955088 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.472+705A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955088 | |||||||
| chr4:55955145 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472+762G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955145 | |||||||
| chr4:55955228 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472+845G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955228 | |||||||
| chr4:55955465 | G | A | 2 | a0001c0001t0005g0124 a0001c0001t0005g0125 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.472+1082G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955465 | |||||||
| chr4:55955640 | C | T | 89 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(86): Show |
98 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.472+1257C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955640 | |||||||
| chr4:55955999 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.473-1224A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55955999 | |||||||
| chr4:55956177 | C | CCTTAAAA others(7): Show |
1 | a0002c0002t0003g0261 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.473-1037_473-1036i others(16): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr4 | 55956177 | ||||||
| chr4:55956222 | A | C | 2 | a0006c0008t0011g0029 a0006c0008t0011g0030 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.473-1001A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956222 | |||||||
| chr4:55956441 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.473-782C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956441 | |||||||
| chr4:55956591 | T | C | 50 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(47): Show |
55 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.473-632T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956591 | |||||||
| chr4:55956695 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.473-528C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956695 | |||||||
| chr4:55956704 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.473-519G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956704 | |||||||
| chr4:55956740 | A | G | 1 | a0001c0003t0003g0274 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.473-483A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956740 | |||||||
| chr4:55956801 | C | T | 1 | a0002c0002t0003g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.473-422C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956801 | |||||||
| chr4:55956825 | C | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.473-398C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956825 | |||||||
| chr4:55956885 | A | G | 1 | a0001c0001t0004g0023 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.473-338A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956885 | |||||||
| chr4:55956913 | C | A | 1 | a0001c0001t0006g0009 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.473-310C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55956913 | |||||||
| chr4:55957158 | G | A | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.473-65G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 4/25 | chr4 | 55957158 | |||||||
| chr4:55957563 | A | G | 4 | a0002c0002t0003g0035 a0002c0002t0003g0160 a0002c0002t0003g0161 others(1): Show |
4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.614+199A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957563 | |||||||
| chr4:55957609 | C | T | 1 | a0005c0006t0008g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.614+245C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957609 | |||||||
| chr4:55957649 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.614+285T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957649 | |||||||
| chr4:55957679 | A | C | 1 | a0006c0008t0011g0030 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.614+315A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55957679 | |||||||
| chr4:55958256 | G | A | 1 | a0001c0015t0004g0284 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.614+892G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958256 | |||||||
| chr4:55958743 | C | T | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.615-939C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958743 | |||||||
| chr4:55958744 | G | A | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.615-938G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958744 | |||||||
| chr4:55958886 | A | T | 32 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(29): Show |
35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.615-796A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55958886 | |||||||
| chr4:55959469 | T | C | 2 | a0001c0001t0004g0285 a0001c0015t0004g0284 |
2 | HG00408.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.615-213T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55959469 | |||||||
| chr4:55959492 | C | CTG | 199 | a0001c0001t0001g0123 a0001c0001t0001g0294 a0001c0001t0002g0005 others(196): Show |
222 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.615-189_615-188ins others(2): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr4 | 55959492 | ||||||
| chr4:55959622 | G | A | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.615-60G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 5/25 | chr4 | 55959622 | |||||||
| chr4:55960067 | T | C | 34 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(31): Show |
37 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+301T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960067 | |||||||
| chr4:55960129 | A | G | 1 | a0001c0001t0006g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.699+363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960129 | |||||||
| chr4:55960300 | TTTTG | T | 23 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0022 others(20): Show |
26 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.699+542_699+545del others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960300 | ||||||
| chr4:55960369 | G | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.699+603G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960369 | |||||||
| chr4:55960913 | G | A | 2 | a0001c0001t0010g0055 a0001c0001t0010g0056 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.699+1147G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960913 | |||||||
| chr4:55960921 | G | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(120): Show |
133 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.699+1155G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960921 | |||||||
| chr4:55960925 | C | CA | 134 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(131): Show |
149 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.699+1183dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | ||||||
| chr4:55960925 | C | CAA | 21 | a0001c0001t0002g0031 a0001c0001t0002g0038 a0001c0001t0002g0039 others(18): Show |
21 | HG00423.hp2 HG01106.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.699+1182_699+1183d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | ||||||
| chr4:55960925 | CA | C | 10 | a0001c0001t0001g0257 a0001c0001t0012g0153 a0001c0001t0012g0154 others(7): Show |
10 | HG01167.hp2 HG01884.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+1183delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55960925 | ||||||
| chr4:55960950 | T | A | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.699+1184T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960950 | |||||||
| chr4:55960988 | C | T | 1 | a0001c0001t0023g0116 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.699+1222C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55960988 | |||||||
| chr4:55961041 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.699+1275G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961041 | |||||||
| chr4:55961101 | C | CA | 15 | a0001c0001t0001g0184 a0001c0001t0001g0188 a0001c0001t0002g0031 others(12): Show |
21 | HG00423.hp2 HG00558.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.699+1354dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | ||||||
| chr4:55961101 | CA | C | 37 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(34): Show |
40 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.699+1354delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | ||||||
| chr4:55961101 | CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.699+1345_699+1354d others(12): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961101 | ||||||
| chr4:55961164 | A | ATGT | 36 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(33): Show |
39 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.699+1401_699+1403d others(5): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961164 | ||||||
| chr4:55961168 | T | G | 3 | a0001c0001t0004g0283 a0001c0001t0004g0295 a0001c0001t0004g0298 |
3 | HG02155.hp2 HG03942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.699+1402T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961168 | |||||||
| chr4:55961181 | T | C | 1 | a0001c0001t0004g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.699+1415T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961181 | |||||||
| chr4:55961183 | T | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.699+1417T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961183 | |||||||
| chr4:55961245 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.699+1479G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961245 | |||||||
| chr4:55961322 | A | G | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+1556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961322 | |||||||
| chr4:55961493 | G | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0092 others(2): Show |
6 | HG02132.hp1 NA18984.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+1727G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961493 | |||||||
| chr4:55961531 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.699+1765G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961531 | |||||||
| chr4:55961624 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.699+1858T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961624 | |||||||
| chr4:55961632 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.699+1866C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961632 | |||||||
| chr4:55961637 | T | C | 2 | a0001c0001t0004g0287 a0001c0001t0004g0288 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.699+1871T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961637 | |||||||
| chr4:55961764 | T | TA | 34 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(31): Show |
34 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.699+2029dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAA | 9 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0167 others(6): Show |
10 | HG00609.hp1 HG01109.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.699+2028_699+2029d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAA | 17 | a0001c0001t0002g0054 a0001c0001t0002g0060 a0001c0001t0002g0082 others(14): Show |
17 | HG00609.hp2 HG01346.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.699+2025_699+2029d others(7): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAA | 26 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0038 others(23): Show |
30 | HG00423.hp2 HG01070.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.699+2024_699+2029d others(8): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA | 16 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0051 others(13): Show |
17 | HG00140.hp1 HG00642.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.699+2023_699+2029d others(9): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA others(1): Show |
13 | a0001c0001t0002g0011 a0001c0001t0002g0063 a0001c0001t0002g0064 others(10): Show |
14 | HG02080.hp2 HG02145.hp1 HG03579.hp1 others(11): Show |
intron_variant | MODIFIER | c.699+2022_699+2029d others(10): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA others(2): Show |
6 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0092 others(3): Show |
6 | HG00673.hp2 HG03927.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+2021_699+2029d others(11): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA others(3): Show |
6 | a0001c0001t0002g0012 a0001c0001t0002g0024 a0001c0001t0002g0069 others(3): Show |
7 | HG01358.hp2 HG02132.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+2020_699+2029d others(12): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA others(4): Show |
1 | a0001c0001t0002g0061 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.699+2019_699+2029d others(13): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0068 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.699+2018_699+2029d others(14): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TA | T | 41 | a0001c0001t0001g0165 a0001c0001t0001g0181 a0001c0001t0001g0182 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.699+2029delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAA | T | 17 | a0001c0001t0001g0256 a0001c0001t0007g0004 a0001c0001t0007g0028 others(14): Show |
19 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.699+2028_699+2029d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAAA | T | 32 | a0002c0002t0003g0002 a0002c0002t0003g0015 a0002c0002t0003g0035 others(29): Show |
37 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.699+2027_699+2029d others(5): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.699+2019_699+2029d others(13): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAAAAAAA others(8): Show |
T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.699+2015_699+2029d others(17): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAAAAAAA others(9): Show |
T | 1 | a0001c0001t0022g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.699+2014_699+2029d others(18): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961764 | TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0006g0050 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699+2013_699+2029d others(19): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55961764 | ||||||
| chr4:55961765 | A | T | 2 | a0001c0001t0004g0292 a0001c0001t0004g0293 |
2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.699+1999A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961765 | |||||||
| chr4:55961766 | A | T | 1 | a0001c0001t0005g0125 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.699+2000A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961766 | |||||||
| chr4:55961823 | T | C | 1 | a0002c0002t0003g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.699+2057T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961823 | |||||||
| chr4:55961830 | T | C | 2 | a0001c0001t0005g0235 a0001c0001t0005g0236 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.699+2064T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961830 | |||||||
| chr4:55961966 | T | C | 8 | a0001c0001t0004g0021 a0001c0001t0004g0275 a0001c0001t0004g0285 others(5): Show |
9 | HG00408.hp1 HG02083.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+2200T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55961966 | |||||||
| chr4:55962106 | A | AT | 9 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 others(6): Show |
14 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.700-2157dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962106 | ||||||
| chr4:55962106 | AT | A | 41 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0014 others(38): Show |
46 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.700-2157delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962106 | ||||||
| chr4:55962131 | C | G | 188 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(185): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.700-2143C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962131 | |||||||
| chr4:55962351 | C | T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.700-1923C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962351 | |||||||
| chr4:55962464 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.700-1810C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962464 | |||||||
| chr4:55962482 | A | G | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700-1792A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962482 | |||||||
| chr4:55962500 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.700-1774C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962500 | |||||||
| chr4:55962603 | G | A | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.700-1671G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962603 | |||||||
| chr4:55962683 | CT | C | 187 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(184): Show |
209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.700-1589delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962683 | ||||||
| chr4:55962708 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.700-1566C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962708 | |||||||
| chr4:55962714 | T | G | 45 | a0001c0001t0019g0278 a0001c0001t0031g0129 a0002c0002t0003g0002 others(42): Show |
52 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.700-1560T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55962714 | |||||||
| chr4:55962730 | C | CT | 8 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
8 | HG01884.hp2 HG02258.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.700-1530dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | ||||||
| chr4:55962730 | C | CTT | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.700-1531_700-1530d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | ||||||
| chr4:55962730 | CT | C | 169 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0002g0005 others(166): Show |
186 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.700-1530delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr4 | 55962730 | ||||||
| chr4:55963195 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.700-1079T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963195 | |||||||
| chr4:55963316 | G | A | 197 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(194): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.700-958G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963316 | |||||||
| chr4:55963511 | C | T | 1 | a0002c0002t0003g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.700-763C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963511 | |||||||
| chr4:55963619 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.700-655A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963619 | |||||||
| chr4:55963788 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.700-486T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55963788 | |||||||
| chr4:55964143 | C | T | 3 | a0002c0002t0003g0014 a0002c0002t0003g0147 a0002c0002t0015g0014 |
3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.700-131C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964143 | |||||||
| chr4:55964151 | T | G | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.700-123T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964151 | |||||||
| chr4:55964171 | A | T | 1 | a0001c0001t0006g0009 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.700-103A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 6/25 | chr4 | 55964171 | |||||||
| chr4:55964439 | A | G | 7 | a0002c0002t0003g0035 a0002c0002t0003g0130 a0002c0002t0003g0146 others(4): Show |
7 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.828+37A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964439 | |||||||
| chr4:55964482 | G | C | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.828+80G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964482 | |||||||
| chr4:55964649 | G | T | 1 | a0002c0002t0003g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.828+247G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964649 | |||||||
| chr4:55964768 | G | A | 40 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0014 others(37): Show |
45 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.828+366G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964768 | |||||||
| chr4:55964930 | C | T | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.828+528C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964930 | |||||||
| chr4:55964958 | A | G | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.828+556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55964958 | |||||||
| chr4:55965167 | C | T | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-477C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965167 | |||||||
| chr4:55965280 | G | A | 187 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(184): Show |
209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.829-364G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965280 | |||||||
| chr4:55965423 | T | C | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.829-221T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 7/25 | chr4 | 55965423 | |||||||
| chr4:55965881 | T | A | 1 | a0001c0001t0016g0175 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1044+22T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55965881 | |||||||
| chr4:55965938 | C | G | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1044+79C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55965938 | |||||||
| chr4:55966007 | C | T | 38 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(35): Show |
41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1044+148C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966007 | |||||||
| chr4:55966163 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1044+304G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966163 | |||||||
| chr4:55966205 | C | CT | 33 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1044+355dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55966205 | ||||||
| chr4:55966318 | A | G | 9 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 others(6): Show |
14 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1044+459A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966318 | |||||||
| chr4:55966328 | A | C | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044+469A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966328 | |||||||
| chr4:55966371 | T | C | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044+512T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966371 | |||||||
| chr4:55966501 | T | C | 1 | a0002c0002t0003g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1044+642T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966501 | |||||||
| chr4:55966555 | C | G | 128 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(125): Show |
140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1044+696C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966555 | |||||||
| chr4:55966739 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1044+880T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966739 | |||||||
| chr4:55966959 | C | A | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1044+1100C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55966959 | |||||||
| chr4:55967097 | G | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044+1238G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967097 | |||||||
| chr4:55967601 | T | G | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1045-1462T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967601 | |||||||
| chr4:55967719 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1045-1344C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967719 | |||||||
| chr4:55967950 | A | G | 2 | a0001c0001t0002g0069 a0001c0001t0002g0071 |
2 | NA18952.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1045-1113A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55967950 | |||||||
| chr4:55968204 | A | T | 1 | a0002c0002t0003g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1045-859A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968204 | |||||||
| chr4:55968220 | T | G | 188 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(185): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1045-843T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968220 | |||||||
| chr4:55968235 | T | C | 5 | a0001c0001t0004g0021 a0001c0001t0004g0296 a0001c0001t0004g0297 others(2): Show |
6 | NA18961.hp1 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-828T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968235 | |||||||
| chr4:55968347 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1045-716C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968347 | |||||||
| chr4:55968368 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-695A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968368 | |||||||
| chr4:55968374 | G | GT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0230 a0001c0001t0002g0081 others(7): Show |
10 | HG01167.hp2 HG01981.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1045-673dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | ||||||
| chr4:55968374 | GT | G | 95 | a0001c0001t0001g0206 a0001c0001t0002g0011 a0001c0001t0002g0012 others(92): Show |
106 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1045-673delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | ||||||
| chr4:55968374 | GTT | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-674_1045-673d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | INFO_REALIGN_3_PRIME | chr4 | 55968374 | ||||||
| chr4:55968651 | T | C | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1045-412T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968651 | |||||||
| chr4:55968671 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1045-392A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968671 | |||||||
| chr4:55968689 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1045-374T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968689 | |||||||
| chr4:55968832 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1045-231C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968832 | |||||||
| chr4:55968844 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1045-219T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968844 | |||||||
| chr4:55968877 | C | T | 3 | a0001c0001t0002g0120 a0001c0001t0014g0033 a0001c0001t0014g0034 |
3 | HG02717.hp1 HG02976.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1045-186C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968877 | |||||||
| chr4:55968878 | G | A | 1 | a0001c0001t0005g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1045-185G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968878 | |||||||
| chr4:55968938 | T | A | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1045-125T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968938 | |||||||
| chr4:55968948 | G | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(121): Show |
134 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1045-115G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 8/25 | chr4 | 55968948 | |||||||
| chr4:55969143 | T | C | 32 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1110+15T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969143 | |||||||
| chr4:55969247 | C | T | 197 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(194): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1110+119C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969247 | |||||||
| chr4:55969277 | A | G | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1110+149A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969277 | |||||||
| chr4:55969428 | TA | T | 189 | a0001c0001t0001g0174 a0001c0001t0001g0188 a0001c0001t0001g0190 others(186): Show |
211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1110+320delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55969428 | ||||||
| chr4:55969428 | TAA | T | 11 | a0001c0001t0002g0059 a0001c0001t0002g0065 a0001c0001t0002g0090 others(8): Show |
11 | HG01099.hp2 HG01517.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1110+319_1110+320d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55969428 | ||||||
| chr4:55969444 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110+316A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969444 | |||||||
| chr4:55969445 | A | G | 2 | a0001c0001t0019g0278 a0002c0002t0004g0143 |
2 | HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1110+317A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969445 | |||||||
| chr4:55969741 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0121 a0001c0001t0001g0202 others(4): Show |
7 | HG02080.hp1 HG02523.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1110+613A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969741 | |||||||
| chr4:55969904 | G | A | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1110+776G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969904 | |||||||
| chr4:55969909 | G | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0230 |
3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1110+781G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969909 | |||||||
| chr4:55969953 | G | A | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1110+825G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55969953 | |||||||
| chr4:55970037 | C | CT | 186 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(183): Show |
208 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1110+923dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr4 | 55970037 | ||||||
| chr4:55970077 | A | G | 197 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(194): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1110+949A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970077 | |||||||
| chr4:55970123 | C | T | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+995C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970123 | |||||||
| chr4:55970585 | C | T | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1111-685C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970585 | |||||||
| chr4:55970668 | G | A | 2 | a0001c0001t0011g0026 a0011c0012t0008g0179 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1111-602G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970668 | |||||||
| chr4:55970701 | G | T | 2 | a0004c0005t0001g0178 a0011c0012t0008g0179 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1111-569G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970701 | |||||||
| chr4:55970828 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1111-442C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55970828 | |||||||
| chr4:55971205 | ATCTT | A | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111-64_1111-61del others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 9/25 | chr4 | 55971205 | |||||||
| chr4:55971454 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1249+46C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55971454 | |||||||
| chr4:55971926 | G | A | 33 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0022 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1249+518G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55971926 | |||||||
| chr4:55972292 | G | A | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1249+884G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972292 | |||||||
| chr4:55972358 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1249+950G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972358 | |||||||
| chr4:55972365 | TA | T | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1249+960delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr4 | 55972365 | ||||||
| chr4:55972390 | G | C | 1 | a0001c0001t0029g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1249+982G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972390 | |||||||
| chr4:55972486 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1249+1078T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972486 | |||||||
| chr4:55972487 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249+1079A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972487 | |||||||
| chr4:55972629 | C | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0080 a0001c0001t0002g0086 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249+1221C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972629 | |||||||
| chr4:55972749 | A | T | 1 | a0002c0002t0003g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1249+1341A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972749 | |||||||
| chr4:55972759 | C | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | NA18970.hp1 NA18979.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249+1351C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972759 | |||||||
| chr4:55972905 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1249+1497G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972905 | |||||||
| chr4:55972985 | C | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1249+1577C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55972985 | |||||||
| chr4:55973206 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1250-1540C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973206 | |||||||
| chr4:55973280 | G | A | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250-1466G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973280 | |||||||
| chr4:55973539 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1250-1207G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973539 | |||||||
| chr4:55973642 | G | A | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1250-1104G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973642 | |||||||
| chr4:55973700 | A | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
138 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1250-1046A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973700 | |||||||
| chr4:55973874 | G | A | 187 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(184): Show |
209 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1250-872G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55973874 | |||||||
| chr4:55974061 | A | G | 1 | a0001c0001t0005g0252 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1250-685A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974061 | |||||||
| chr4:55974135 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250-611A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974135 | |||||||
| chr4:55974509 | C | T | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250-237C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974509 | |||||||
| chr4:55974584 | T | C | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1250-162T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974584 | |||||||
| chr4:55974664 | A | G | 4 | a0002c0002t0003g0035 a0002c0002t0003g0160 a0002c0002t0003g0161 others(1): Show |
4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-82A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974664 | |||||||
| chr4:55974680 | A | G | 49 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0019g0278 others(46): Show |
56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1250-66A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 10/25 | chr4 | 55974680 | |||||||
| chr4:55975049 | C | T | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+80C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975049 | |||||||
| chr4:55975157 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1473+188A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975157 | |||||||
| chr4:55975901 | G | T | 1 | a0001c0001t0014g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1473+932G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975901 | |||||||
| chr4:55975940 | G | A | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+971G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55975940 | |||||||
| chr4:55976048 | G | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0209 |
2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1473+1079G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976048 | |||||||
| chr4:55976131 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1473+1162C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976131 | |||||||
| chr4:55976235 | CA | C | 27 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(24): Show |
34 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1473+1280delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976235 | ||||||
| chr4:55976246 | A | G | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1473+1277A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976246 | |||||||
| chr4:55976593 | T | C | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1473+1624T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976593 | |||||||
| chr4:55976708 | A | T | 197 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(194): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1473+1739A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976708 | |||||||
| chr4:55976973 | C | CT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0168 a0001c0001t0001g0219 others(5): Show |
9 | HG00280.hp1 HG00733.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+2017dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976973 | ||||||
| chr4:55976973 | CT | C | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1473+2017delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55976973 | ||||||
| chr4:55976979 | T | G | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1473+2010T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976979 | |||||||
| chr4:55976982 | T | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1473+2013T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976982 | |||||||
| chr4:55976983 | T | G | 160 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(157): Show |
175 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1473+2014T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976983 | |||||||
| chr4:55976987 | G | T | 4 | a0001c0001t0001g0205 a0001c0001t0001g0220 a0008c0010t0001g0229 others(1): Show |
4 | NA18955.hp2 NA18989.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1473+2018G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55976987 | |||||||
| chr4:55977005 | A | G | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0188 others(5): Show |
8 | HG01884.hp1 HG02132.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+2036A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977005 | |||||||
| chr4:55977191 | A | G | 2 | a0002c0002t0003g0142 a0002c0002t0003g0144 |
2 | NA19007.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1473+2222A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977191 | |||||||
| chr4:55977601 | T | G | 12 | a0001c0001t0004g0008 a0001c0001t0004g0022 a0001c0001t0004g0023 others(9): Show |
14 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1474-2542T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977601 | |||||||
| chr4:55977760 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1474-2383A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977760 | |||||||
| chr4:55977783 | A | T | 188 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(185): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1474-2360A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977783 | |||||||
| chr4:55977883 | G | C | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-2260G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55977883 | |||||||
| chr4:55978167 | A | AGGGAACT others(13): Show |
1 | a0001c0013t0005g0187 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1474-1974_1474-195 others(24): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55978167 | ||||||
| chr4:55978320 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1474-1823T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978320 | |||||||
| chr4:55978534 | C | G | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1474-1609C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978534 | |||||||
| chr4:55978996 | C | T | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-1147C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55978996 | |||||||
| chr4:55979039 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1474-1104A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979039 | |||||||
| chr4:55979120 | A | G | 49 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0019g0278 others(46): Show |
56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1474-1023A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979120 | |||||||
| chr4:55979122 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1474-1021A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979122 | |||||||
| chr4:55979149 | A | G | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1474-994A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979149 | |||||||
| chr4:55979238 | CT | C | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1474-896delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr4 | 55979238 | ||||||
| chr4:55979604 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1474-539G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979604 | |||||||
| chr4:55979605 | C | T | 34 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(31): Show |
37 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1474-538C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 11/25 | chr4 | 55979605 | |||||||
| chr4:55980401 | T | A | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1626+106T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980401 | |||||||
| chr4:55980585 | A | C | 58 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(55): Show |
65 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.1626+290A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980585 | |||||||
| chr4:55980859 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1627-368G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 12/25 | chr4 | 55980859 | |||||||
| chr4:55981575 | G | T | 1 | a0002c0002t0003g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1779+196G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55981575 | |||||||
| chr4:55981802 | T | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1779+423T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55981802 | |||||||
| chr4:55982023 | T | C | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1779+644T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982023 | |||||||
| chr4:55982147 | C | G | 2 | a0001c0001t0004g0285 a0001c0015t0004g0284 |
2 | HG00408.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1779+768C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982147 | |||||||
| chr4:55982203 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1779+824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982203 | |||||||
| chr4:55982313 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1779+934A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982313 | |||||||
| chr4:55982340 | A | G | 3 | a0001c0001t0002g0104 a0007c0009t0002g0094 a0007c0009t0002g0114 |
3 | HG00140.hp1 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1779+961A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982340 | |||||||
| chr4:55982426 | A | G | 1 | a0001c0001t0005g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1779+1047A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982426 | |||||||
| chr4:55982510 | G | A | 1 | a0001c0001t0022g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1779+1131G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982510 | |||||||
| chr4:55982847 | C | A | 1 | a0013c0018t0018g0269 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1779+1468C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55982847 | |||||||
| chr4:55983149 | T | C | 1 | a0002c0002t0017g0306 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1779+1770T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983149 | |||||||
| chr4:55983218 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1779+1839A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983218 | |||||||
| chr4:55983324 | C | T | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1779+1945C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983324 | |||||||
| chr4:55983453 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1780-1828C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983453 | |||||||
| chr4:55983628 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1780-1653A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983628 | |||||||
| chr4:55983638 | CT | C | 141 | a0001c0001t0001g0174 a0001c0001t0002g0005 a0001c0001t0002g0010 others(138): Show |
151 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1780-1630delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr4 | 55983638 | ||||||
| chr4:55983651 | T | G | 49 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0019g0278 others(46): Show |
56 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1780-1630T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983651 | |||||||
| chr4:55983666 | C | T | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1780-1615C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983666 | |||||||
| chr4:55983706 | A | G | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-1575A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983706 | |||||||
| chr4:55983734 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0209 |
2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1780-1547C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983734 | |||||||
| chr4:55983807 | A | G | 1 | a0001c0001t0013g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1780-1474A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983807 | |||||||
| chr4:55983811 | T | C | 44 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0006 others(41): Show |
51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-1470T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983811 | |||||||
| chr4:55983826 | A | T | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1780-1455A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55983826 | |||||||
| chr4:55984032 | A | G | 44 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0006 others(41): Show |
51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-1249A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984032 | |||||||
| chr4:55984153 | G | A | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-1128G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984153 | |||||||
| chr4:55984246 | A | T | 43 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0031 others(40): Show |
45 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(42): Show |
intron_variant | MODIFIER | c.1780-1035A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984246 | |||||||
| chr4:55984546 | G | T | 190 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(187): Show |
212 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1780-735G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984546 | |||||||
| chr4:55984680 | A | G | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1780-601A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984680 | |||||||
| chr4:55984730 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0109 a0001c0001t0002g0113 |
3 | HG00642.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1780-551A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984730 | |||||||
| chr4:55984786 | C | G | 1 | a0003c0004t0003g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1780-495C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984786 | |||||||
| chr4:55984837 | C | T | 1 | a0001c0001t0002g0112 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1780-444C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984837 | |||||||
| chr4:55984857 | G | T | 44 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0006 others(41): Show |
51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-424G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984857 | |||||||
| chr4:55984872 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1780-409C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984872 | |||||||
| chr4:55984982 | G | C | 6 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(3): Show |
8 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1780-299G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984982 | |||||||
| chr4:55984993 | A | G | 40 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0031 others(37): Show |
42 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.1780-288A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55984993 | |||||||
| chr4:55985061 | A | T | 44 | a0001c0001t0031g0129 a0002c0002t0003g0002 a0002c0002t0003g0006 others(41): Show |
51 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1780-220A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55985061 | |||||||
| chr4:55985241 | T | C | 1 | a0001c0001t0014g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1780-40T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 13/25 | chr4 | 55985241 | |||||||
| chr4:55985425 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1857+67A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985425 | |||||||
| chr4:55985430 | CTA | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0230 |
3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1857+74_1857+75del others(2): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55985430 | ||||||
| chr4:55985558 | G | A | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1857+200G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985558 | |||||||
| chr4:55985700 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1857+342A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55985700 | |||||||
| chr4:55986020 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1857+662G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986020 | |||||||
| chr4:55986124 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1857+766C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986124 | |||||||
| chr4:55986130 | G | A | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1857+772G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986130 | |||||||
| chr4:55986174 | A | G | 43 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0014 others(40): Show |
50 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1857+816A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986174 | |||||||
| chr4:55986181 | C | T | 4 | a0001c0001t0005g0218 a0001c0001t0005g0244 a0001c0001t0005g0246 others(1): Show |
4 | HG00738.hp1 HG01993.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857+823C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986181 | |||||||
| chr4:55986302 | C | T | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1857+944C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986302 | |||||||
| chr4:55986334 | G | C | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1857+976G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55986334 | |||||||
| chr4:55987043 | A | G | 83 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(80): Show |
88 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1857+1685A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987043 | |||||||
| chr4:55987096 | G | A | 1 | a0001c0001t0004g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1857+1738G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987096 | |||||||
| chr4:55987325 | G | A | 3 | a0002c0002t0003g0014 a0002c0002t0003g0147 a0002c0002t0015g0014 |
3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1857+1967G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987325 | |||||||
| chr4:55987472 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1857+2114A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987472 | |||||||
| chr4:55987474 | A | G | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1857+2116A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987474 | |||||||
| chr4:55987591 | G | A | 188 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(185): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1857+2233G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987591 | |||||||
| chr4:55987805 | G | C | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0011g0026 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1857+2447G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987805 | |||||||
| chr4:55987810 | G | A | 1 | a0001c0001t0014g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1857+2452G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987810 | |||||||
| chr4:55987919 | A | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0217 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1857+2561A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55987919 | |||||||
| chr4:55988003 | A | G | 1 | a0001c0001t0007g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1857+2645A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988003 | |||||||
| chr4:55988084 | T | C | 1 | a0002c0002t0017g0306 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1857+2726T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988084 | |||||||
| chr4:55988145 | G | GT | 189 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(186): Show |
211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1857+2788dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988145 | ||||||
| chr4:55988165 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1857+2807T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988165 | |||||||
| chr4:55988228 | G | A | 43 | a0001c0001t0002g0109 a0002c0002t0003g0002 a0002c0002t0003g0006 others(40): Show |
50 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1857+2870G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988228 | |||||||
| chr4:55988261 | C | T | 1 | a0002c0002t0003g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1857+2903C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988261 | |||||||
| chr4:55988402 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1857+3044G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988402 | |||||||
| chr4:55988661 | G | GA | 120 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(117): Show |
130 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1858-3260dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988661 | ||||||
| chr4:55988661 | GA | G | 6 | a0001c0001t0001g0177 a0001c0001t0001g0189 a0001c0001t0001g0200 others(3): Show |
6 | HG00741.hp2 HG01516.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1858-3260delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988661 | ||||||
| chr4:55988687 | G | T | 1 | a0001c0001t0004g0295 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1858-3247G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988687 | |||||||
| chr4:55988753 | C | T | 1 | a0001c0001t0004g0298 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1858-3181C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988753 | |||||||
| chr4:55988773 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1858-3161C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988773 | |||||||
| chr4:55988817 | C | T | 3 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0016t0027g0276 |
5 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-3117C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988817 | |||||||
| chr4:55988818 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0209 |
2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1858-3116G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988818 | |||||||
| chr4:55988831 | G | C | 1 | a0001c0001t0005g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1858-3103G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988831 | |||||||
| chr4:55988853 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1858-3081C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988853 | |||||||
| chr4:55988894 | G | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1858-3040G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988894 | |||||||
| chr4:55988935 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1858-2999C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988935 | |||||||
| chr4:55988966 | G | GA | 17 | a0001c0001t0002g0095 a0001c0001t0002g0110 a0001c0001t0002g0186 others(14): Show |
17 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1858-2954dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55988966 | ||||||
| chr4:55988989 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1858-2945A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55988989 | |||||||
| chr4:55989021 | C | T | 2 | a0001c0001t0007g0004 a0001c0001t0007g0028 |
4 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1858-2913C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989021 | |||||||
| chr4:55989044 | G | A | 9 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(6): Show |
9 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1858-2890G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989044 | |||||||
| chr4:55989076 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-2858A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989076 | |||||||
| chr4:55989349 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0264 others(1): Show |
5 | HG00558.hp1 HG00609.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-2585T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989349 | |||||||
| chr4:55989354 | T | C | 8 | a0001c0001t0005g0180 a0001c0001t0005g0210 a0001c0001t0005g0218 others(5): Show |
8 | HG00738.hp1 HG01515.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-2580T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989354 | |||||||
| chr4:55989366 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1858-2568A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989366 | |||||||
| chr4:55989447 | G | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0279 a0001c0001t0004g0280 others(2): Show |
5 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1858-2487G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989447 | |||||||
| chr4:55989501 | A | G | 189 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(186): Show |
211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1858-2433A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989501 | |||||||
| chr4:55989651 | A | G | 43 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0014 others(40): Show |
50 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1858-2283A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55989651 | |||||||
| chr4:55990004 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1858-1930T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990004 | |||||||
| chr4:55990053 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1858-1881T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990053 | |||||||
| chr4:55990208 | T | C | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1858-1726T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990208 | |||||||
| chr4:55990543 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1858-1391C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990543 | |||||||
| chr4:55990544 | G | A | 81 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1858-1390G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990544 | |||||||
| chr4:55990609 | C | G | 3 | a0001c0001t0013g0267 a0001c0001t0013g0268 a0001c0001t0020g0266 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1858-1325C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990609 | |||||||
| chr4:55990677 | T | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0177 a0001c0001t0001g0253 others(2): Show |
5 | NA18970.hp1 NA18977.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1858-1257T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990677 | |||||||
| chr4:55990701 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1858-1233C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990701 | |||||||
| chr4:55990703 | G | A | 188 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(185): Show |
210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1858-1231G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990703 | |||||||
| chr4:55990849 | G | C | 189 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(186): Show |
211 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1858-1085G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990849 | |||||||
| chr4:55990943 | T | A | 1 | a0001c0001t0005g0025 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1858-991T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990943 | |||||||
| chr4:55990973 | A | G | 1 | a0001c0001t0004g0283 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1858-961A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55990973 | |||||||
| chr4:55990980 | CT | C | 43 | a0001c0001t0001g0224 a0001c0001t0004g0008 a0001c0001t0004g0021 others(40): Show |
46 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1858-941delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55990980 | ||||||
| chr4:55991109 | A | G | 2 | a0006c0008t0011g0029 a0006c0008t0011g0030 |
2 | HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1858-825A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991109 | |||||||
| chr4:55991177 | C | T | 3 | a0001c0001t0014g0033 a0001c0001t0014g0034 a0001c0001t0019g0278 |
3 | HG02647.hp2 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1858-757C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991177 | |||||||
| chr4:55991178 | G | A | 1 | a0001c0001t0004g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1858-756G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991178 | |||||||
| chr4:55991190 | A | G | 1 | a0001c0001t0004g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1858-744A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991190 | |||||||
| chr4:55991318 | CT | C | 35 | a0001c0001t0002g0081 a0001c0001t0004g0008 a0001c0001t0004g0021 others(32): Show |
38 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1858-601delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr4 | 55991318 | ||||||
| chr4:55991324 | T | C | 1 | a0013c0018t0018g0269 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-610T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991324 | |||||||
| chr4:55991409 | T | A | 1 | a0001c0001t0012g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1858-525T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991409 | |||||||
| chr4:55991436 | T | C | 1 | a0002c0002t0003g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1858-498T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991436 | |||||||
| chr4:55991841 | G | C | 82 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(79): Show |
88 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1858-93G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991841 | |||||||
| chr4:55991921 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1858-13A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 14/25 | chr4 | 55991921 | |||||||
| chr4:55992169 | T | G | 6 | a0001c0001t0002g0010 a0001c0001t0002g0080 a0001c0001t0002g0086 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2009+84T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992169 | |||||||
| chr4:55992284 | A | G | 46 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0014 others(43): Show |
53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2009+199A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992284 | |||||||
| chr4:55992448 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2009+363A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992448 | |||||||
| chr4:55992455 | T | A | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+370T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992455 | |||||||
| chr4:55992460 | T | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+375T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992460 | |||||||
| chr4:55992471 | G | T | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+386G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992471 | |||||||
| chr4:55992535 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+450A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992535 | |||||||
| chr4:55992658 | C | T | 2 | a0001c0001t0010g0055 a0001c0001t0010g0056 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2009+573C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992658 | |||||||
| chr4:55992772 | C | T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2009+687C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992772 | |||||||
| chr4:55992889 | G | A | 1 | a0009c0014t0002g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2009+804G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992889 | |||||||
| chr4:55992916 | G | A | 1 | a0001c0001t0004g0301 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2009+831G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992916 | |||||||
| chr4:55992932 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0200 |
2 | HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2009+847C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55992932 | |||||||
| chr4:55993080 | A | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0082 |
2 | NA18950.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2009+995A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993080 | |||||||
| chr4:55993244 | C | T | 1 | a0001c0001t0022g0115 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2009+1159C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993244 | |||||||
| chr4:55993335 | T | C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+1250T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993335 | |||||||
| chr4:55993385 | C | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2009+1300C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993385 | |||||||
| chr4:55993634 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+1549A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993634 | |||||||
| chr4:55993641 | C | T | 1 | a0002c0002t0003g0043 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2009+1556C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993641 | |||||||
| chr4:55993811 | G | A | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2009+1726G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55993811 | |||||||
| chr4:55994135 | T | C | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2009+2050T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994135 | |||||||
| chr4:55994587 | C | T | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2009+2502C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994587 | |||||||
| chr4:55994656 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2009+2571A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994656 | |||||||
| chr4:55994672 | A | G | 8 | a0001c0001t0006g0032 a0001c0001t0006g0044 a0001c0001t0006g0045 others(5): Show |
8 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.2009+2587A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994672 | |||||||
| chr4:55994686 | CT | C | 8 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0206 others(5): Show |
8 | HG01168.hp1 HG01934.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.2009+2618delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55994686 | ||||||
| chr4:55994718 | C | T | 81 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(78): Show |
86 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.2009+2633C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994718 | |||||||
| chr4:55994846 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+2761C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994846 | |||||||
| chr4:55994849 | A | G | 5 | a0002c0002t0003g0006 a0002c0002t0003g0089 a0002c0002t0003g0117 others(2): Show |
7 | NA18961.hp2 NA18979.hp1 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.2009+2764A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994849 | |||||||
| chr4:55994878 | G | A | 1 | a0002c0002t0003g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2009+2793G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994878 | |||||||
| chr4:55994907 | A | G | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+2822A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994907 | |||||||
| chr4:55994980 | T | C | 203 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(200): Show |
226 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.2009+2895T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55994980 | |||||||
| chr4:55995142 | T | A | 1 | a0002c0002t0003g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2009+3057T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995142 | |||||||
| chr4:55995144 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2009+3059C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995144 | |||||||
| chr4:55995307 | C | T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2009+3222C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995307 | |||||||
| chr4:55995392 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2009+3307G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995392 | |||||||
| chr4:55995493 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2009+3408C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995493 | |||||||
| chr4:55995641 | A | G | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2009+3556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995641 | |||||||
| chr4:55995706 | C | T | 1 | a0005c0006t0008g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2010-3596C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995706 | |||||||
| chr4:55995719 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2010-3583C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55995719 | |||||||
| chr4:55996714 | C | CT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0217 others(3): Show |
7 | HG01975.hp2 HG01981.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.2010-2574dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55996714 | ||||||
| chr4:55996922 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2010-2380A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55996922 | |||||||
| chr4:55996952 | A | T | 2 | a0001c0001t0007g0004 a0001c0001t0007g0028 |
4 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2010-2350A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55996952 | |||||||
| chr4:55997045 | C | G | 1 | a0008c0010t0001g0229 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2010-2257C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997045 | |||||||
| chr4:55997054 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2010-2248G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997054 | |||||||
| chr4:55997173 | T | G | 1 | a0001c0001t0001g0224 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2010-2129T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997173 | |||||||
| chr4:55997696 | G | GT | 201 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2010-1599dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55997696 | ||||||
| chr4:55997747 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2010-1555G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997747 | |||||||
| chr4:55997775 | A | C | 2 | a0001c0001t0019g0278 a0001c0001t0031g0129 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2010-1527A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997775 | |||||||
| chr4:55997848 | A | G | 1 | a0002c0002t0003g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2010-1454A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997848 | |||||||
| chr4:55997866 | A | G | 56 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(53): Show |
63 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.2010-1436A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997866 | |||||||
| chr4:55997868 | T | G | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-1434T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55997868 | |||||||
| chr4:55998033 | G | A | 1 | a0001c0001t0024g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2010-1269G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998033 | |||||||
| chr4:55998115 | G | A | 1 | a0001c0001t0012g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2010-1187G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998115 | |||||||
| chr4:55998148 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2010-1154G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998148 | |||||||
| chr4:55998211 | A | G | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2010-1091A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998211 | |||||||
| chr4:55998335 | A | G | 115 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(112): Show |
123 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.2010-967A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998335 | |||||||
| chr4:55998457 | CT | C | 3 | a0001c0001t0014g0033 a0001c0001t0014g0034 a0001c0016t0027g0276 |
3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2010-841delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr4 | 55998457 | ||||||
| chr4:55998597 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2010-705G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998597 | |||||||
| chr4:55998794 | G | C | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2010-508G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998794 | |||||||
| chr4:55998880 | A | G | 17 | a0001c0001t0002g0031 a0001c0001t0002g0038 a0001c0001t0002g0039 others(14): Show |
17 | HG00423.hp2 HG03654.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.2010-422A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998880 | |||||||
| chr4:55998971 | C | A | 38 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(35): Show |
41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.2010-331C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55998971 | |||||||
| chr4:55999139 | A | G | 2 | a0001c0001t0002g0070 a0001c0001t0002g0072 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2010-163A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999139 | |||||||
| chr4:55999146 | T | C | 1 | a0002c0002t0003g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2010-156T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999146 | |||||||
| chr4:55999157 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2010-145A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999157 | |||||||
| chr4:55999194 | C | A | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2010-108C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 15/25 | chr4 | 55999194 | |||||||
| chr4:55999855 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2280+210G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999855 | |||||||
| chr4:55999897 | T | A | 1 | a0001c0001t0006g0009 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2280+252T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999897 | |||||||
| chr4:55999997 | C | T | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2280+352C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 55999997 | |||||||
| chr4:56000132 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2280+487C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000132 | |||||||
| chr4:56000316 | C | T | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2280+671C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000316 | |||||||
| chr4:56000343 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0031g0129 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2280+698A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000343 | |||||||
| chr4:56000415 | A | G | 1 | a0001c0001t0004g0301 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2280+770A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000415 | |||||||
| chr4:56000664 | G | A | 2 | a0001c0001t0010g0055 a0001c0001t0010g0056 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+1019G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000664 | |||||||
| chr4:56000704 | T | C | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2280+1059T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000704 | |||||||
| chr4:56000714 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2280+1069G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000714 | |||||||
| chr4:56000804 | T | C | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+1159T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000804 | |||||||
| chr4:56000820 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2280+1175C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000820 | |||||||
| chr4:56000921 | C | A | 8 | a0002c0002t0003g0035 a0002c0002t0003g0130 a0002c0002t0003g0146 others(5): Show |
8 | HG01099.hp2 HG01106.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2280+1276C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56000921 | |||||||
| chr4:56001040 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2280+1395T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56001040 | |||||||
| chr4:56001760 | A | AT | 202 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2280+2124dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56001760 | ||||||
| chr4:56001863 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2280+2218T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56001863 | |||||||
| chr4:56002049 | G | T | 1 | a0001c0001t0024g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2280+2404G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002049 | |||||||
| chr4:56002053 | G | C | 42 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0031 others(39): Show |
44 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.2280+2408G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002053 | |||||||
| chr4:56002176 | A | G | 80 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(77): Show |
85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2280+2531A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002176 | |||||||
| chr4:56002386 | C | T | 202 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2280+2741C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002386 | |||||||
| chr4:56002479 | A | G | 1 | a0001c0001t0005g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2280+2834A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56002479 | |||||||
| chr4:56003051 | T | C | 87 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
94 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2280+3406T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003051 | |||||||
| chr4:56003122 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2280+3477A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003122 | |||||||
| chr4:56003123 | C | T | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+3478C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003123 | |||||||
| chr4:56003165 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0257 |
3 | HG03098.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2280+3520A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003165 | |||||||
| chr4:56003273 | C | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0077 a0001c0001t0002g0079 others(1): Show |
4 | NA18975.hp2 NA19062.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280+3628C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003273 | |||||||
| chr4:56003320 | C | T | 2 | a0001c0001t0010g0055 a0001c0001t0010g0056 |
2 | HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2280+3675C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003320 | |||||||
| chr4:56003353 | C | G | 1 | a0001c0001t0006g0046 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2280+3708C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003353 | |||||||
| chr4:56003459 | C | T | 46 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0014 others(43): Show |
53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2280+3814C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003459 | |||||||
| chr4:56003460 | G | A | 1 | a0001c0001t0004g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2280+3815G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003460 | |||||||
| chr4:56003468 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2280+3823A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003468 | |||||||
| chr4:56003584 | A | G | 251 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0164 others(248): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2280+3939A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003584 | |||||||
| chr4:56003659 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2280+4014G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003659 | |||||||
| chr4:56003670 | A | G | 4 | a0002c0002t0003g0035 a0002c0002t0003g0160 a0002c0002t0003g0161 others(1): Show |
4 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2280+4025A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003670 | |||||||
| chr4:56003720 | TG | T | 3 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 |
3 | HG02280.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2280+4076delG | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003720 | |||||||
| chr4:56003726 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0193 |
3 | HG00558.hp1 HG00609.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2280+4081T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003726 | |||||||
| chr4:56003729 | T | C | 1 | a0002c0002t0003g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2280+4084T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003729 | |||||||
| chr4:56003780 | G | A | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2280+4135G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003780 | |||||||
| chr4:56003909 | C | T | 1 | a0002c0002t0003g0160 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2280+4264C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56003909 | |||||||
| chr4:56004179 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0200 |
2 | HG00741.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2281-4148G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004179 | |||||||
| chr4:56004289 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2281-4038A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004289 | |||||||
| chr4:56004479 | A | T | 36 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(33): Show |
39 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2281-3848A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004479 | |||||||
| chr4:56004625 | C | A | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2281-3702C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004625 | |||||||
| chr4:56004678 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2281-3649A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004678 | |||||||
| chr4:56004926 | A | AT | 97 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0184 others(94): Show |
104 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2281-3383dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | ||||||
| chr4:56004926 | A | ATT | 16 | a0001c0001t0002g0005 a0001c0001t0002g0060 a0001c0001t0002g0067 others(13): Show |
18 | HG01175.hp2 HG01928.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.2281-3384_2281-338 others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | ||||||
| chr4:56004926 | A | T | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2281-3401A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56004926 | |||||||
| chr4:56004926 | AT | A | 13 | a0001c0001t0001g0193 a0001c0001t0001g0257 a0001c0001t0005g0252 others(10): Show |
14 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.2281-3383delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | ||||||
| chr4:56004926 | ATT | A | 11 | a0001c0001t0031g0129 a0001c0003t0003g0003 a0001c0003t0003g0020 others(8): Show |
17 | HG00558.hp2 HG00639.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.2281-3384_2281-338 others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | ||||||
| chr4:56004926 | ATTT | A | 52 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(49): Show |
58 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.2281-3385_2281-338 others(7): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56004926 | ||||||
| chr4:56005216 | C | G | 201 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2281-3111C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005216 | |||||||
| chr4:56005391 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2281-2936C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005391 | |||||||
| chr4:56005397 | G | A | 38 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(35): Show |
41 | HG00140.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.2281-2930G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005397 | |||||||
| chr4:56005514 | G | T | 1 | a0001c0001t0002g0112 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2281-2813G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005514 | |||||||
| chr4:56005722 | G | A | 74 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(71): Show |
87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2281-2605G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005722 | |||||||
| chr4:56005739 | A | G | 1 | a0001c0001t0004g0275 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2281-2588A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005739 | |||||||
| chr4:56005758 | G | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2281-2569G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005758 | |||||||
| chr4:56005873 | A | G | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2281-2454A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005873 | |||||||
| chr4:56005926 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2281-2401C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56005926 | |||||||
| chr4:56006362 | T | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0206 others(4): Show |
7 | HG02132.hp2 HG02735.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.2281-1965T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006362 | |||||||
| chr4:56006450 | T | C | 2 | a0001c0001t0004g0286 a0001c0001t0004g0289 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2281-1877T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006450 | |||||||
| chr4:56006500 | C | T | 3 | a0001c0001t0004g0291 a0001c0001t0004g0292 a0001c0001t0004g0293 |
3 | HG02280.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2281-1827C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006500 | |||||||
| chr4:56006503 | A | G | 88 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(85): Show |
95 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2281-1824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006503 | |||||||
| chr4:56006533 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2281-1794G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006533 | |||||||
| chr4:56006629 | T | A | 1 | a0001c0001t0002g0075 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2281-1698T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006629 | |||||||
| chr4:56006718 | G | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2281-1609G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006718 | |||||||
| chr4:56006791 | A | G | 46 | a0002c0002t0003g0002 a0002c0002t0003g0006 a0002c0002t0003g0014 others(43): Show |
53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2281-1536A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006791 | |||||||
| chr4:56006862 | G | T | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2281-1465G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006862 | |||||||
| chr4:56006926 | C | T | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-1401C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006926 | |||||||
| chr4:56006985 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2281-1342C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56006985 | |||||||
| chr4:56007050 | C | T | 1 | a0001c0001t0002g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2281-1277C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007050 | |||||||
| chr4:56007075 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2281-1252G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007075 | |||||||
| chr4:56007077 | A | C | 1 | a0001c0001t0006g0009 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2281-1250A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007077 | |||||||
| chr4:56007124 | TCTCAGGT others(11): Show |
T | 1 | a0002c0002t0003g0126 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2281-1197_2281-118 others(22): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr4 | 56007124 | ||||||
| chr4:56007292 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2281-1035T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007292 | |||||||
| chr4:56007446 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2281-881C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007446 | |||||||
| chr4:56007528 | G | A | 2 | a0001c0001t0004g0279 a0001c0001t0004g0280 |
2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2281-799G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007528 | |||||||
| chr4:56007678 | A | G | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-649A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007678 | |||||||
| chr4:56007748 | G | C | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2281-579G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007748 | |||||||
| chr4:56007790 | T | C | 202 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2281-537T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007790 | |||||||
| chr4:56007808 | T | C | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2281-519T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007808 | |||||||
| chr4:56007888 | T | C | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0007g0052 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2281-439T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007888 | |||||||
| chr4:56007907 | T | C | 12 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0024 others(9): Show |
14 | HG02132.hp1 NA18956.hp2 NA18957.hp1 others(11): Show |
intron_variant | MODIFIER | c.2281-420T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007907 | |||||||
| chr4:56007914 | G | A | 1 | a0001c0001t0024g0305 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2281-413G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007914 | |||||||
| chr4:56007941 | C | T | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2281-386C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56007941 | |||||||
| chr4:56008076 | G | A | 74 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(71): Show |
87 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2281-251G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56008076 | |||||||
| chr4:56008115 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2281-212G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 17/25 | chr4 | 56008115 | |||||||
| chr4:56008435 | C | T | 2 | a0001c0001t0020g0266 a0001c0001t0031g0129 |
2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2336+53C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008435 | |||||||
| chr4:56008485 | A | G | 3 | a0001c0001t0014g0033 a0001c0001t0014g0034 a0001c0016t0027g0276 |
3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2336+103A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008485 | |||||||
| chr4:56008612 | A | G | 1 | a0001c0001t0005g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2336+230A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008612 | |||||||
| chr4:56008767 | T | C | 1 | a0002c0002t0003g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2336+385T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008767 | |||||||
| chr4:56008844 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2336+462A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56008844 | |||||||
| chr4:56009045 | T | C | 42 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0031 others(39): Show |
44 | HG00423.hp2 HG00609.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.2336+663T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009045 | |||||||
| chr4:56009091 | A | G | 201 | a0001c0001t0001g0294 a0001c0001t0002g0005 a0001c0001t0002g0010 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2337-644A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009091 | |||||||
| chr4:56009155 | G | T | 197 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(194): Show |
220 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.2337-580G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009155 | |||||||
| chr4:56009158 | G | T | 3 | a0001c0001t0002g0270 a0001c0001t0004g0290 a0001c0001t0006g0049 |
3 | HG03130.hp1 HG03710.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2337-577G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009158 | |||||||
| chr4:56009167 | G | T | 252 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0164 others(249): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2337-568G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009167 | |||||||
| chr4:56009198 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2337-537G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009198 | |||||||
| chr4:56009223 | G | A | 1 | a0001c0001t0006g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2337-512G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009223 | |||||||
| chr4:56009225 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | NA19076.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2337-510G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009225 | |||||||
| chr4:56009246 | C | T | 1 | a0002c0002t0003g0137 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2337-489C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009246 | |||||||
| chr4:56009303 | C | G | 87 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(84): Show |
102 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2337-432C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009303 | |||||||
| chr4:56009338 | A | G | 1 | a0002c0002t0003g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2337-397A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009338 | |||||||
| chr4:56009641 | G | A | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2337-94G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009641 | |||||||
| chr4:56009663 | A | G | 33 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2337-72A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 18/25 | chr4 | 56009663 | |||||||
| chr4:56010075 | C | T | 15 | a0001c0001t0004g0298 a0001c0001t0006g0009 a0001c0001t0006g0032 others(12): Show |
21 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.2505+172C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010075 | |||||||
| chr4:56010175 | AC | A | 57 | a0001c0001t0001g0199 a0001c0001t0002g0011 a0001c0001t0002g0012 others(54): Show |
66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.2505+282delC | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010175 | ||||||
| chr4:56010175 | ACC | A | 148 | a0001c0001t0001g0171 a0001c0001t0001g0195 a0001c0001t0002g0005 others(145): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2505+281_2505+282d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010175 | ||||||
| chr4:56010176 | C | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | NA19076.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2505+273C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010176 | |||||||
| chr4:56010178 | C | G | 1 | a0001c0001t0005g0216 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2505+275C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010178 | |||||||
| chr4:56010179 | C | G | 1 | a0001c0001t0005g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2505+276C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010179 | |||||||
| chr4:56010179 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2505+276C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010179 | |||||||
| chr4:56010246 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2505+343C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010246 | |||||||
| chr4:56010310 | C | T | 2 | a0001c0001t0019g0278 a0001c0001t0031g0129 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2505+407C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010310 | |||||||
| chr4:56010311 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0020g0266 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2505+408G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010311 | |||||||
| chr4:56010360 | CA | C | 190 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(187): Show |
208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2505+475delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010360 | ||||||
| chr4:56010362 | A | C | 9 | a0001c0001t0002g0104 a0001c0001t0006g0009 a0001c0001t0006g0032 others(6): Show |
10 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.2505+459A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010362 | |||||||
| chr4:56010410 | AAACACAT others(18): Show |
A | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2505+509_2505+533d others(27): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr4 | 56010410 | ||||||
| chr4:56010495 | A | G | 1 | a0001c0001t0005g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2505+592A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010495 | |||||||
| chr4:56010624 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2505+721A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010624 | |||||||
| chr4:56010697 | T | C | 2 | a0001c0001t0004g0286 a0001c0001t0004g0289 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2506-715T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010697 | |||||||
| chr4:56010712 | C | T | 1 | a0001c0001t0004g0304 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2506-700C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56010712 | |||||||
| chr4:56011125 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2506-287C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011125 | |||||||
| chr4:56011157 | C | G | 4 | a0001c0001t0001g0177 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | NA18970.hp1 NA18979.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2506-255C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011157 | |||||||
| chr4:56011300 | C | G | 5 | a0001c0001t0004g0021 a0001c0001t0004g0296 a0001c0001t0004g0297 others(2): Show |
6 | NA18961.hp1 NA18977.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.2506-112C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 19/25 | chr4 | 56011300 | |||||||
| chr4:56011559 | G | T | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2616+37G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | chr4 | 56011559 | |||||||
| chr4:56011559 | GT | G | 31 | a0001c0001t0002g0080 a0001c0001t0004g0008 a0001c0001t0004g0021 others(28): Show |
34 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2616+51delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr4 | 56011559 | ||||||
| chr4:56011688 | A | G | 1 | a0001c0016t0027g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2617-112A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 20/25 | chr4 | 56011688 | |||||||
| chr4:56012027 | A | G | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+42A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012027 | |||||||
| chr4:56012067 | A | T | 3 | a0001c0001t0001g0256 a0007c0009t0002g0094 a0007c0009t0002g0114 |
3 | HG01358.hp2 HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2802+82A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012067 | |||||||
| chr4:56012071 | T | A | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2802+86T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012071 | |||||||
| chr4:56012088 | G | T | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2802+103G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012088 | |||||||
| chr4:56012275 | C | T | 1 | a0001c0001t0021g0122 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2802+290C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012275 | |||||||
| chr4:56012298 | C | T | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+313C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012298 | |||||||
| chr4:56012424 | A | G | 1 | a0002c0002t0003g0233 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2802+439A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012424 | |||||||
| chr4:56012505 | T | A | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2802+520T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012505 | |||||||
| chr4:56012596 | G | A | 1 | a0002c0002t0003g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2802+611G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012596 | |||||||
| chr4:56012634 | GT | G | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+652delT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 56012634 | ||||||
| chr4:56012758 | G | A | 1 | a0001c0001t0005g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2802+773G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012758 | |||||||
| chr4:56012989 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2802+1004T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56012989 | |||||||
| chr4:56013039 | A | G | 2 | a0001c0003t0003g0271 a0001c0003t0003g0272 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2802+1054A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013039 | |||||||
| chr4:56013047 | G | T | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+1062G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013047 | |||||||
| chr4:56013082 | C | T | 3 | a0002c0002t0003g0014 a0002c0002t0003g0147 a0002c0002t0015g0014 |
3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2802+1097C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013082 | |||||||
| chr4:56013300 | C | T | 202 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2802+1315C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013300 | |||||||
| chr4:56013383 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2802+1398G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013383 | |||||||
| chr4:56013494 | A | G | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+1509A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013494 | |||||||
| chr4:56013543 | T | G | 5 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0092 others(2): Show |
6 | HG02132.hp1 NA18984.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.2802+1558T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013543 | |||||||
| chr4:56013697 | C | T | 1 | a0010c0011t0005g0163 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2802+1712C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013697 | |||||||
| chr4:56013965 | A | G | 1 | a0013c0018t0018g0269 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2802+1980A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013965 | |||||||
| chr4:56013966 | C | T | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2802+1981C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56013966 | |||||||
| chr4:56014023 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2802+2038A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014023 | |||||||
| chr4:56014100 | T | C | 1 | a0001c0001t0004g0302 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2802+2115T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014100 | |||||||
| chr4:56014133 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0265 |
2 | HG01884.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2802+2148C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014133 | |||||||
| chr4:56014177 | T | A | 33 | a0001c0001t0001g0294 a0001c0001t0004g0008 a0001c0001t0004g0021 others(30): Show |
36 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2802+2192T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014177 | |||||||
| chr4:56014246 | A | G | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2802+2261A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014246 | |||||||
| chr4:56014250 | CAAACACC others(3): Show |
C | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2802+2269_2802+227 others(14): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr4 | 56014250 | ||||||
| chr4:56014611 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2802+2626A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014611 | |||||||
| chr4:56014646 | A | G | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.2802+2661A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014646 | |||||||
| chr4:56014708 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2802+2723A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014708 | |||||||
| chr4:56014736 | G | A | 5 | a0002c0002t0003g0043 a0002c0002t0003g0128 a0002c0002t0003g0133 others(2): Show |
7 | HG00738.hp2 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.2802+2751G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014736 | |||||||
| chr4:56014822 | A | C | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0007g0052 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2803-2826A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014822 | |||||||
| chr4:56014857 | A | C | 87 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(84): Show |
94 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2803-2791A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014857 | |||||||
| chr4:56014878 | G | T | 1 | a0001c0001t0005g0247 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2803-2770G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014878 | |||||||
| chr4:56014986 | G | A | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.2803-2662G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56014986 | |||||||
| chr4:56015042 | A | C | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2803-2606A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015042 | |||||||
| chr4:56015052 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2803-2596A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015052 | |||||||
| chr4:56015116 | C | T | 202 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.2803-2532C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015116 | |||||||
| chr4:56015169 | A | T | 1 | a0001c0001t0005g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2803-2479A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015169 | |||||||
| chr4:56015185 | C | T | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2803-2463C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015185 | |||||||
| chr4:56015459 | G | A | 1 | a0002c0002t0006g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2803-2189G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015459 | |||||||
| chr4:56015528 | G | C | 5 | a0001c0001t0004g0008 a0001c0001t0004g0279 a0001c0001t0004g0280 others(2): Show |
5 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.2803-2120G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015528 | |||||||
| chr4:56015558 | A | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2803-2090A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56015558 | |||||||
| chr4:56016151 | G | C | 201 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.2803-1497G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016151 | |||||||
| chr4:56016514 | G | A | 1 | a0002c0002t0003g0263 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2803-1134G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016514 | |||||||
| chr4:56016577 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2803-1071G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016577 | |||||||
| chr4:56016666 | A | G | 1 | a0003c0004t0003g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2803-982A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016666 | |||||||
| chr4:56016709 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0199 a0001c0001t0001g0213 others(1): Show |
4 | NA19001.hp2 NA19009.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-939A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016709 | |||||||
| chr4:56016888 | G | A | 1 | a0001c0001t0011g0027 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2803-760G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56016888 | |||||||
| chr4:56017094 | G | T | 1 | a0001c0001t0002g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2803-554G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017094 | |||||||
| chr4:56017204 | G | A | 4 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(1): Show |
4 | HG01255.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-444G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017204 | |||||||
| chr4:56017591 | G | A | 4 | a0001c0001t0002g0068 a0001c0001t0002g0076 a0001c0001t0002g0088 others(1): Show |
4 | HG00609.hp2 HG01934.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.2803-57G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 21/25 | chr4 | 56017591 | |||||||
| chr4:56017913 | T | C | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3012+56T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56017913 | |||||||
| chr4:56017959 | G | A | 1 | a0001c0001t0011g0026 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3012+102G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56017959 | |||||||
| chr4:56018050 | G | A | 1 | a0001c0001t0005g0246 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3012+193G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018050 | |||||||
| chr4:56018068 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3012+211A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018068 | |||||||
| chr4:56018166 | G | A | 32 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.3012+309G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018166 | |||||||
| chr4:56018243 | G | T | 4 | a0001c0001t0011g0026 a0001c0001t0011g0027 a0006c0008t0011g0029 others(1): Show |
4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3012+386G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018243 | |||||||
| chr4:56018249 | G | A | 1 | a0001c0001t0011g0027 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3012+392G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018249 | |||||||
| chr4:56018283 | A | G | 202 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.3012+426A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018283 | |||||||
| chr4:56018340 | A | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0001g0169 others(11): Show |
15 | HG00423.hp1 HG01069.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3012+483A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018340 | |||||||
| chr4:56018438 | C | G | 2 | a0001c0001t0013g0267 a0001c0001t0013g0268 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3012+581C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018438 | |||||||
| chr4:56018524 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3012+667G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018524 | |||||||
| chr4:56018664 | A | G | 201 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.3013-689A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018664 | |||||||
| chr4:56018692 | C | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3013-661C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56018692 | |||||||
| chr4:56018759 | C | CA | 7 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0007g0052 others(4): Show |
9 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013-583dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | INFO_REALIGN_3_PRIME | chr4 | 56018759 | ||||||
| chr4:56019082 | C | A | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3013-271C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 22/25 | chr4 | 56019082 | |||||||
| chr4:56019588 | A | G | 3 | a0002c0002t0003g0014 a0002c0002t0003g0147 a0002c0002t0015g0014 |
3 | HG03098.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3215+33A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019588 | |||||||
| chr4:56019720 | G | C | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.3215+165G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019720 | |||||||
| chr4:56019798 | G | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3215+243G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019798 | |||||||
| chr4:56019800 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3215+245G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019800 | |||||||
| chr4:56019809 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3215+254C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019809 | |||||||
| chr4:56019844 | C | A | 2 | a0001c0001t0004g0286 a0001c0001t0004g0289 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3215+289C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019844 | |||||||
| chr4:56019845 | G | A | 10 | a0001c0001t0001g0201 a0001c0001t0006g0009 a0001c0001t0006g0032 others(7): Show |
11 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.3215+290G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019845 | |||||||
| chr4:56019909 | A | T | 80 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(77): Show |
85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.3215+354A>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019909 | |||||||
| chr4:56019931 | G | A | 1 | a0001c0001t0009g0211 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3215+376G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019931 | |||||||
| chr4:56019996 | C | T | 16 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0184 others(13): Show |
17 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.3215+441C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019996 | |||||||
| chr4:56019997 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3215+442G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56019997 | |||||||
| chr4:56020142 | G | A | 201 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.3216-534G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020142 | |||||||
| chr4:56020290 | T | C | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3216-386T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020290 | |||||||
| chr4:56020530 | A | G | 1 | a0003c0004t0003g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3216-146A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020530 | |||||||
| chr4:56020614 | C | T | 13 | a0001c0001t0002g0012 a0001c0001t0002g0061 a0001c0001t0002g0063 others(10): Show |
14 | HG00673.hp2 HG02080.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.3216-62C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 23/25 | chr4 | 56020614 | |||||||
| chr4:56020846 | T | C | 4 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(1): Show |
4 | HG01255.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.3320+66T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56020846 | |||||||
| chr4:56020976 | G | A | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.3320+196G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56020976 | |||||||
| chr4:56021028 | A | C | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3320+248A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021028 | |||||||
| chr4:56021088 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3320+308G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021088 | |||||||
| chr4:56021453 | G | A | 1 | a0001c0001t0006g0009 | 2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3320+673G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021453 | |||||||
| chr4:56021534 | C | T | 1 | a0001c0001t0010g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3320+754C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021534 | |||||||
| chr4:56021763 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0113 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3320+983G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56021763 | |||||||
| chr4:56022060 | G | A | 32 | a0001c0001t0004g0008 a0001c0001t0004g0021 a0001c0001t0004g0022 others(29): Show |
35 | HG00408.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.3320+1280G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022060 | |||||||
| chr4:56022272 | G | A | 1 | a0001c0001t0004g0291 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3320+1492G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022272 | |||||||
| chr4:56022389 | G | T | 1 | a0001c0001t0006g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3320+1609G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022389 | |||||||
| chr4:56022622 | G | A | 3 | a0002c0002t0003g0015 a0002c0002t0003g0138 a0003c0004t0003g0139 |
4 | HG00639.hp2 HG00733.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3320+1842G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022622 | |||||||
| chr4:56022677 | A | G | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.3321-1824A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022677 | |||||||
| chr4:56022951 | G | A | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3321-1550G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022951 | |||||||
| chr4:56022992 | G | A | 1 | a0002c0002t0003g0135 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3321-1509G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56022992 | |||||||
| chr4:56023012 | G | A | 1 | a0002c0002t0006g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3321-1489G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023012 | |||||||
| chr4:56023049 | T | G | 1 | a0001c0001t0012g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3321-1452T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023049 | |||||||
| chr4:56023094 | A | G | 5 | a0002c0002t0003g0043 a0002c0002t0003g0128 a0002c0002t0003g0133 others(2): Show |
7 | HG00738.hp2 HG02055.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.3321-1407A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023094 | |||||||
| chr4:56023119 | G | C | 1 | a0001c0001t0005g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3321-1382G>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023119 | |||||||
| chr4:56023139 | G | A | 1 | a0002c0002t0006g0148 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3321-1362G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023139 | |||||||
| chr4:56023208 | C | CA | 4 | a0001c0001t0011g0026 a0001c0001t0011g0027 a0006c0008t0011g0029 others(1): Show |
4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3321-1291dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023208 | ||||||
| chr4:56023221 | C | CA | 58 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0031 others(55): Show |
66 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.3321-1269dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023221 | ||||||
| chr4:56023272 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3321-1229A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023272 | |||||||
| chr4:56023470 | A | C | 3 | a0001c0001t0019g0278 a0001c0001t0020g0266 a0001c0001t0031g0129 |
3 | HG02109.hp1 HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3321-1031A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023470 | |||||||
| chr4:56023507 | C | A | 1 | a0001c0001t0002g0098 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3321-994C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023507 | |||||||
| chr4:56023572 | G | A | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3321-929G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023572 | |||||||
| chr4:56023688 | AAT | A | 80 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(77): Show |
85 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.3321-803_3321-802d others(4): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023688 | ||||||
| chr4:56023688 | AATAT | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0264 others(1): Show |
5 | HG00558.hp1 HG00609.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.3321-805_3321-802d others(6): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56023688 | ||||||
| chr4:56023707 | G | A | 202 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(199): Show |
225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.3321-794G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023707 | |||||||
| chr4:56023752 | T | C | 1 | a0001c0001t0011g0027 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3321-749T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56023752 | |||||||
| chr4:56024132 | ATATAATT others(2): Show |
A | 4 | a0001c0001t0011g0026 a0001c0001t0011g0027 a0006c0008t0011g0029 others(1): Show |
4 | HG01243.hp2 HG02300.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3321-355_3321-347d others(11): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr4 | 56024132 | ||||||
| chr4:56024368 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3321-133A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 24/25 | chr4 | 56024368 | |||||||
| chr4:56024660 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*11+46A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56024660 | |||||||
| chr4:56024764 | A | G | 8 | a0001c0001t0001g0184 a0001c0001t0005g0018 a0001c0001t0005g0025 others(5): Show |
9 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.*11+150A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56024764 | |||||||
| chr4:56024825 | C | CT | 46 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(43): Show |
53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.*11+225dupT | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56024825 | ||||||
| chr4:56025094 | G | A | 3 | a0001c0001t0007g0004 a0001c0001t0007g0028 a0001c0001t0007g0052 |
5 | HG02258.hp1 HG02280.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.*11+480G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025094 | |||||||
| chr4:56025101 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.*11+487T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025101 | |||||||
| chr4:56025727 | A | C | 1 | a0001c0001t0014g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.*11+1113A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025727 | |||||||
| chr4:56025775 | A | G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*11+1161A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025775 | |||||||
| chr4:56025876 | T | G | 1 | a0002c0002t0003g0261 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*11+1262T>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025876 | |||||||
| chr4:56025907 | C | A | 85 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(82): Show |
92 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.*11+1293C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025907 | |||||||
| chr4:56025907 | C | CA | 45 | a0001c0001t0001g0221 a0001c0001t0002g0092 a0001c0001t0004g0008 others(42): Show |
48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.*11+1308dupA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56025907 | ||||||
| chr4:56025946 | C | A | 3 | a0002c0002t0003g0127 a0002c0002t0003g0137 a0002c0002t0003g0145 |
3 | HG02129.hp1 NA18952.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.*11+1332C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025946 | |||||||
| chr4:56025999 | A | G | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*11+1385A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56025999 | |||||||
| chr4:56026163 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0304 |
3 | HG01975.hp2 HG01981.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.*11+1549C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026163 | |||||||
| chr4:56026165 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.*11+1551C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026165 | |||||||
| chr4:56026183 | T | A | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.*11+1569T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026183 | |||||||
| chr4:56026317 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0217 |
2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.*11+1703A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026317 | |||||||
| chr4:56026529 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.*11+1915T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026529 | |||||||
| chr4:56026558 | C | T | 1 | a0001c0001t0031g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.*11+1944C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026558 | |||||||
| chr4:56026931 | A | G | 1 | a0002c0002t0003g0150 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.*11+2317A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56026931 | |||||||
| chr4:56027003 | C | T | 46 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(43): Show |
53 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.*11+2389C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027003 | |||||||
| chr4:56027201 | T | C | 3 | a0001c0001t0019g0278 a0001c0001t0020g0266 a0001c0001t0031g0129 |
3 | HG02109.hp1 HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.*11+2587T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027201 | |||||||
| chr4:56027296 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0031g0129 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.*11+2682A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027296 | |||||||
| chr4:56027356 | C | G | 1 | a0001c0001t0005g0218 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*11+2742C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027356 | |||||||
| chr4:56027520 | A | G | 2 | a0005c0006t0008g0157 a0011c0012t0008g0179 |
2 | HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.*11+2906A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56027520 | |||||||
| chr4:56028073 | C | G | 3 | a0005c0006t0008g0152 a0005c0006t0008g0155 a0005c0006t0008g0159 |
3 | HG02976.hp2 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.*12-3287C>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028073 | |||||||
| chr4:56028153 | A | G | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-3207A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028153 | |||||||
| chr4:56028252 | G | T | 1 | a0004c0005t0001g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*12-3108G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028252 | |||||||
| chr4:56028610 | GA | G | 7 | a0001c0001t0001g0245 a0001c0001t0002g0012 a0001c0001t0002g0063 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.*12-2737delA | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56028610 | ||||||
| chr4:56028630 | G | T | 1 | a0001c0001t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*12-2730G>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028630 | |||||||
| chr4:56028653 | A | G | 10 | a0001c0001t0012g0153 a0001c0001t0012g0154 a0001c0001t0012g0156 others(7): Show |
10 | HG01167.hp2 HG01255.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-2707A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028653 | |||||||
| chr4:56028704 | T | C | 47 | a0001c0001t0003g0185 a0002c0002t0003g0002 a0002c0002t0003g0006 others(44): Show |
54 | HG00408.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.*12-2656T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028704 | |||||||
| chr4:56028717 | A | G | 1 | a0001c0001t0019g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*12-2643A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028717 | |||||||
| chr4:56028804 | A | G | 3 | a0001c0001t0014g0033 a0001c0001t0014g0034 a0001c0016t0027g0276 |
3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*12-2556A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028804 | |||||||
| chr4:56028865 | T | C | 9 | a0001c0001t0006g0009 a0001c0001t0006g0032 a0001c0001t0006g0044 others(6): Show |
10 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.*12-2495T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028865 | |||||||
| chr4:56028934 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.*12-2426T>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56028934 | |||||||
| chr4:56029014 | A | G | 2 | a0001c0001t0006g0045 a0001c0001t0006g0050 |
2 | HG00280.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.*12-2346A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029014 | |||||||
| chr4:56029077 | A | G | 3 | a0001c0001t0014g0033 a0001c0001t0014g0034 a0001c0016t0027g0276 |
3 | HG02717.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.*12-2283A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029077 | |||||||
| chr4:56029160 | C | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0209 a0001c0001t0001g0227 others(1): Show |
4 | HG01069.hp2 HG01109.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.*12-2200C>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029160 | |||||||
| chr4:56029781 | G | A | 201 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(198): Show |
224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.*12-1579G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029781 | |||||||
| chr4:56029842 | A | C | 8 | a0001c0001t0005g0180 a0001c0001t0005g0210 a0001c0001t0005g0218 others(5): Show |
8 | HG00738.hp1 HG01515.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.*12-1518A>C | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029842 | |||||||
| chr4:56029875 | T | A | 2 | a0001c0001t0004g0022 a0001c0001t0004g0304 |
3 | HG01975.hp2 HG01981.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.*12-1485T>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56029875 | |||||||
| chr4:56030253 | A | G | 1 | a0001c0001t0004g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.*12-1107A>G | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030253 | |||||||
| chr4:56030413 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*12-947G>A | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030413 | |||||||
| chr4:56030477 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0004g0293 |
2 | HG03471.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.*12-883C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030477 | |||||||
| chr4:56030782 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.*12-578C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030782 | |||||||
| chr4:56030961 | C | T | 1 | a0001c0001t0020g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*12-399C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56030961 | |||||||
| chr4:56031039 | GAAGGATC others(18): Show |
G | 6 | a0001c0003t0003g0003 a0001c0003t0003g0020 a0001c0003t0003g0271 others(3): Show |
11 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*12-317_*12-293del others(25): Show |
CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr4 | 56031039 | ||||||
| chr4:56031088 | C | T | 79 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(76): Show |
84 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.*12-272C>T | CEP135 | ENSG00000174799.12 | transcript | ENST00000257287.5 | protein_coding | 25/25 | chr4 | 56031088 |