Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 132864 |
| ensemblid | ENSG00000137449.17 |
| hgncid | 21745 |
| symbol | CPEB2 |
| name | cytoplasmic polyadenylation element binding protein 2 |
| refseq_nuc | NM_001177382.2 |
| refseq_prot | NP_001170853.1 |
| ensembl_nuc | ENST00000538197.7 |
| ensembl_prot | ENSP00000443985.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 15002481 |
| end | 15070151 |
| strand | + |
| ver | v1.2 |
| region | chr4:15002481-15070151 |
| region5000 | chr4:14997481-15075151 |
| regionname0 | CPEB2_chr4_15002481_15070151 |
| regionname5000 | CPEB2_chr4_14997481_15075151 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1034 | 112 | 20 | 24 | 52 | 6 | 10 | 38 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0002 | 0/0 | 1037 | 54 | 23 | 3 | 23 | 0 | 5 | 19 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1032): Show |
chr4 | 14997481 | 15075151 |
| a0003 | 1/1 | 1034 | 34 | 7 | 7 | 4 | 3 | 11 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0004 | 0/0 | 1034 | 14 | 0 | 3 | 7 | 0 | 4 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0005 | 0/0 | 1035 | 13 | 4 | 1 | 5 | 1 | 2 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1030): Show |
chr4 | 14997481 | 15075151 |
| a0006 | 0/0 | 1034 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0007 | 0/0 | 1034 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0008 | 0/0 | 1034 | 7 | 0 | 5 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0009 | 0/0 | 1034 | 7 | 0 | 3 | 0 | 0 | 4 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0010 | 0/0 | 1034 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0011 | 0/0 | 1038 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1033): Show |
chr4 | 14997481 | 15075151 |
| a0012 | 0/0 | 1029 | 5 | 0 | 1 | 4 | 0 | 0 | 3 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1024): Show |
chr4 | 14997481 | 15075151 |
| a0013 | 0/0 | 1035 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1030): Show |
chr4 | 14997481 | 15075151 |
| a0014 | 0/0 | 1035 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1030): Show |
chr4 | 14997481 | 15075151 |
| a0015 | 0/0 | 1034 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0016 | 0/0 | 1037 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1032): Show |
chr4 | 14997481 | 15075151 |
| a0017 | 0/0 | 1034 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0018 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| a0019 | 0/0 | 1034 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | MRDFG others(1029): Show |
chr4 | 14997481 | 15075151 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3102 | 110 | 19 | 24 | 51 | 6 | 10 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0001c0026 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0001c0028 | 0/0 | 3102 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0002c0002 | 0/0 | 3111 | 39 | 23 | 3 | 11 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0002c0006 | 0/0 | 3111 | 9 | 0 | 0 | 7 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0002c0015 | 0/0 | 3111 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0002c0017 | 0/0 | 3111 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0002c0021 | 0/0 | 3111 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0003c0003 | 1/1 | 3102 | 33 | 6 | 7 | 4 | 3 | 11 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0003c0030 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0004c0004 | 0/0 | 3102 | 14 | 0 | 3 | 7 | 0 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0005c0005 | 0/0 | 3105 | 13 | 4 | 1 | 5 | 1 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3100): Show |
chr4 | 14997481 | 15075151 | ||
| a0006c0007 | 0/0 | 3102 | 7 | 7 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0006c0012 | 0/0 | 3102 | 5 | 5 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0007c0013 | 0/0 | 3102 | 5 | 5 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0007c0016 | 0/0 | 3102 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0008c0008 | 0/0 | 3102 | 7 | 0 | 5 | 0 | 2 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0009c0009 | 0/0 | 3102 | 7 | 0 | 3 | 0 | 0 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0010c0010 | 0/0 | 3102 | 6 | 6 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0010c0025 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0011c0011 | 0/0 | 3114 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3109): Show |
chr4 | 14997481 | 15075151 | ||
| a0012c0014 | 0/0 | 3087 | 5 | 0 | 1 | 4 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3082): Show |
chr4 | 14997481 | 15075151 | ||
| a0013c0018 | 0/0 | 3105 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3100): Show |
chr4 | 14997481 | 15075151 | ||
| a0013c0022 | 0/0 | 3105 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3100): Show |
chr4 | 14997481 | 15075151 | ||
| a0014c0019 | 0/0 | 3105 | 2 | 1 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3100): Show |
chr4 | 14997481 | 15075151 | ||
| a0015c0029 | 0/0 | 3102 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0016c0020 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3106): Show |
chr4 | 14997481 | 15075151 | ||
| a0017c0027 | 0/0 | 3102 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0018c0024 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 | ||
| a0019c0023 | 0/0 | 3102 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | ATGAG others(3097): Show |
chr4 | 14997481 | 15075151 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7069 | 15 | 12 | 0 | 0 | 0 | 3 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0002 | 0/0 | 7069 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0003 | 0/0 | 7070 | 50 | 5 | 16 | 17 | 6 | 6 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0004 | 0/0 | 7069 | 39 | 1 | 6 | 32 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0018 | 0/0 | 7070 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0019 | 0/0 | 7070 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0022 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0023 | 0/0 | 7070 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0001c0001t0025 | 0/0 | 7070 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0001c0026t0001 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0001c0028t0004 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0002c0002t0002 | 0/0 | 7078 | 36 | 21 | 3 | 10 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0002t0014 | 0/0 | 7078 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0002t0015 | 0/0 | 7078 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0002t0020 | 0/0 | 7078 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0006t0002 | 0/0 | 7078 | 7 | 0 | 0 | 5 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0006t0010 | 0/0 | 7078 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0015t0002 | 0/0 | 7078 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0017t0002 | 0/0 | 7078 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0002c0021t0002 | 0/0 | 7078 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0003c0003t0001 | 1/1 | 7069 | 31 | 6 | 7 | 2 | 3 | 11 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0003c0003t0017 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0003c0003t0021 | 0/0 | 7069 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0003c0030t0001 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0004c0004t0006 | 0/0 | 7067 | 13 | 0 | 3 | 6 | 0 | 4 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7062): Show |
chr4 | 14997481 | 15075151 |
| a0004c0004t0024 | 0/0 | 7067 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7062): Show |
chr4 | 14997481 | 15075151 |
| a0005c0005t0005 | 0/0 | 7072 | 13 | 4 | 1 | 5 | 1 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7067): Show |
chr4 | 14997481 | 15075151 |
| a0006c0007t0008 | 0/0 | 7064 | 5 | 5 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7059): Show |
chr4 | 14997481 | 15075151 |
| a0006c0007t0013 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0006c0007t0026 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGGC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0006c0012t0001 | 0/0 | 7069 | 4 | 4 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0006c0012t0016 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0007c0013t0009 | 0/0 | 7069 | 5 | 5 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0007c0016t0001 | 0/0 | 7069 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0008c0008t0001 | 0/0 | 7069 | 7 | 0 | 5 | 0 | 2 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0009c0009t0001 | 0/0 | 7069 | 6 | 0 | 3 | 0 | 0 | 3 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0009c0009t0011 | 0/0 | 7069 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0010c0010t0007 | 0/0 | 7064 | 6 | 6 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7059): Show |
chr4 | 14997481 | 15075151 |
| a0010c0025t0012 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7051): Show |
chr4 | 14997481 | 15075151 |
| a0011c0011t0002 | 0/0 | 7081 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7076): Show |
chr4 | 14997481 | 15075151 |
| a0012c0014t0004 | 0/0 | 7054 | 5 | 0 | 1 | 4 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7049): Show |
chr4 | 14997481 | 15075151 |
| a0013c0018t0001 | 0/0 | 7072 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7067): Show |
chr4 | 14997481 | 15075151 |
| a0013c0022t0001 | 0/0 | 7072 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7067): Show |
chr4 | 14997481 | 15075151 |
| a0014c0019t0001 | 0/0 | 7072 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7067): Show |
chr4 | 14997481 | 15075151 |
| a0014c0019t0003 | 0/0 | 7073 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7068): Show |
chr4 | 14997481 | 15075151 |
| a0015c0029t0003 | 0/0 | 7070 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7065): Show |
chr4 | 14997481 | 15075151 |
| a0016c0020t0002 | 0/0 | 7078 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7073): Show |
chr4 | 14997481 | 15075151 |
| a0017c0027t0001 | 0/0 | 7069 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0018c0024t0001 | 0/0 | 7069 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7064): Show |
chr4 | 14997481 | 15075151 |
| a0019c0023t0007 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | GCGAC others(7059): Show |
chr4 | 14997481 | 15075151 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0004 | 0/0 | 6 | 1 | 2 | 1 | 1 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0014 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0001 | 0/0 | 11 | 1 | 3 | 7 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0019g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0023g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0001t0025g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0026t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0001c0028t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0005 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0002t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0006t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0006t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0006t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0006t0010g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0015t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0015t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0015t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0017t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0002c0021t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0017g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0003t0021g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0003c0030t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0004c0004t0024g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0005c0005t0005g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0007t0026g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0012t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0012t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0006c0012t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0013t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0013t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0013t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0013t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0013t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0016t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0016t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0007c0016t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0008c0008t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0009c0009t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0009c0009t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0009c0009t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0009c0009t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0009c0009t0011g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0010t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0010t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0010t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0010t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0010t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0010c0025t0012g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0011c0011t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0011c0011t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0012c0014t0004g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0012c0014t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0012c0014t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0013c0018t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0013c0018t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0013c0022t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0014c0019t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0014c0019t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0015c0029t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0016c0020t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0017c0027t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0018c0024t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| a0019c0023t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0027 | EUR | GBR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0179 | EUR | GBR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00140 | hp2 | a0008 | c0008 | t0001 | g0028 | EUR | GBR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0181 | EUR | FIN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00323 | hp2 | a0005 | c0005 | t0005 | g0039 | EUR | FIN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00408 | hp2 | a0002 | c0015 | t0002 | g0078 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00423 | hp1 | a0005 | c0005 | t0005 | g0042 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00423 | hp2 | a0004 | c0004 | t0006 | g0017 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00609 | hp2 | a0004 | c0004 | t0006 | g0057 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0141 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00673 | hp1 | a0011 | c0011 | t0002 | g0002 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00733 | hp2 | a0008 | c0008 | t0001 | g0134 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00735 | hp1 | a0009 | c0009 | t0001 | g0126 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00735 | hp2 | a0015 | c0029 | t0003 | g0194 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00738 | hp1 | a0008 | c0008 | t0001 | g0013 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG00741 | hp2 | a0008 | c0008 | t0001 | g0132 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01069 | hp1 | a0008 | c0008 | t0001 | g0112 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0125 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01081 | hp1 | a0004 | c0004 | t0006 | g0055 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0118 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0117 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01109 | hp2 | a0016 | c0020 | t0002 | g0005 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0123 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01175 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01175 | hp2 | a0017 | c0027 | t0001 | g0133 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01256 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01258 | hp2 | a0009 | c0009 | t0001 | g0012 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01346 | hp1 | a0001 | c0001 | t0019 | g0032 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01346 | hp2 | a0008 | c0008 | t0001 | g0028 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01358 | hp2 | a0004 | c0004 | t0006 | g0051 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0113 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01433 | hp2 | a0012 | c0014 | t0004 | g0003 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01515 | hp1 | a0008 | c0008 | t0001 | g0111 | EUR | IBS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0162 | EUR | IBS | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01884 | hp2 | a0010 | c0010 | t0007 | g0102 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01891 | hp1 | a0013 | c0018 | t0001 | g0106 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01975 | hp1 | a0005 | c0005 | t0005 | g0016 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0131 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0140 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02056 | hp1 | a0002 | c0015 | t0002 | g0062 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02129 | hp1 | a0001 | c0001 | t0022 | g0196 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02129 | hp2 | a0001 | c0001 | t0025 | g0008 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02145 | hp1 | a0002 | c0002 | t0014 | g0079 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02165 | hp1 | a0004 | c0004 | t0006 | g0017 | EAS | CDX | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02257 | hp1 | a0006 | c0007 | t0008 | g0089 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02257 | hp2 | a0010 | c0010 | t0007 | g0011 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0071 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02258 | hp2 | a0006 | c0007 | t0008 | g0024 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02280 | hp1 | a0006 | c0007 | t0013 | g0099 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02280 | hp2 | a0001 | c0026 | t0001 | g0161 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02451 | hp2 | a0007 | c0016 | t0001 | g0046 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02523 | hp1 | a0012 | c0014 | t0004 | g0034 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02523 | hp2 | a0003 | c0003 | t0017 | g0114 | EAS | KHV | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02615 | hp1 | a0007 | c0016 | t0001 | g0048 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0006 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02622 | hp1 | a0010 | c0010 | t0007 | g0103 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02622 | hp2 | a0014 | c0019 | t0001 | g0109 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02630 | hp1 | a0005 | c0005 | t0005 | g0041 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02630 | hp2 | a0006 | c0007 | t0008 | g0024 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02647 | hp1 | a0002 | c0002 | t0020 | g0049 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02647 | hp2 | a0006 | c0007 | t0026 | g0090 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02698 | hp1 | a0003 | c0003 | t0001 | g0029 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02723 | hp1 | a0013 | c0018 | t0001 | g0107 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0115 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02809 | hp1 | a0010 | c0010 | t0007 | g0101 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02818 | hp1 | a0007 | c0013 | t0009 | g0097 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02895 | hp2 | a0006 | c0012 | t0001 | g0010 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02896 | hp1 | a0005 | c0005 | t0005 | g0038 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02896 | hp2 | a0006 | c0012 | t0001 | g0010 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02897 | hp1 | a0005 | c0005 | t0005 | g0037 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02897 | hp2 | a0006 | c0012 | t0001 | g0010 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0064 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02970 | hp1 | a0006 | c0007 | t0008 | g0092 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02970 | hp2 | a0003 | c0030 | t0001 | g0143 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02976 | hp1 | a0007 | c0016 | t0001 | g0047 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0085 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03017 | hp1 | a0003 | c0003 | t0001 | g0013 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03017 | hp2 | a0004 | c0004 | t0006 | g0050 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03098 | hp2 | a0018 | c0024 | t0001 | g0087 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03130 | hp1 | a0007 | c0013 | t0009 | g0091 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03139 | hp1 | a0007 | c0013 | t0009 | g0093 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03195 | hp2 | a0005 | c0005 | t0005 | g0040 | AFR | ESN | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03209 | hp1 | a0007 | c0013 | t0009 | g0095 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03209 | hp2 | a0006 | c0007 | t0008 | g0088 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03225 | hp2 | a0010 | c0010 | t0007 | g0011 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03239 | hp1 | a0005 | c0005 | t0005 | g0016 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0124 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0136 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03490 | hp1 | a0009 | c0009 | t0001 | g0026 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03491 | hp2 | a0004 | c0004 | t0006 | g0018 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03492 | hp1 | a0004 | c0004 | t0006 | g0018 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03492 | hp2 | a0009 | c0009 | t0001 | g0026 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0137 | AFR | GWD | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03654 | hp1 | a0005 | c0005 | t0005 | g0044 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0121 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03704 | hp2 | a0004 | c0004 | t0006 | g0052 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0122 | SAS | PJL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03834 | hp1 | a0002 | c0006 | t0002 | g0021 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0120 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03942 | hp2 | a0002 | c0021 | t0002 | g0002 | SAS | BEB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04199 | hp1 | a0002 | c0006 | t0002 | g0021 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0029 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0027 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG04228 | hp2 | a0009 | c0009 | t0011 | g0012 | SAS | STU | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18522 | hp1 | a0019 | c0023 | t0007 | g0011 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18522 | hp2 | a0006 | c0012 | t0001 | g0096 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CHB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CHB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18906 | hp2 | a0010 | c0010 | t0007 | g0104 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18939 | hp2 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18942 | hp2 | a0004 | c0004 | t0006 | g0053 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18961 | hp2 | a0004 | c0004 | t0006 | g0058 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18962 | hp2 | a0011 | c0011 | t0002 | g0077 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0199 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18969 | hp2 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18972 | hp1 | a0002 | c0015 | t0002 | g0084 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18972 | hp2 | a0012 | c0014 | t0004 | g0034 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18973 | hp1 | a0011 | c0011 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18977 | hp2 | a0014 | c0019 | t0003 | g0192 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18979 | hp1 | a0002 | c0017 | t0002 | g0019 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18979 | hp2 | a0001 | c0028 | t0004 | g0003 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18980 | hp1 | a0004 | c0004 | t0006 | g0045 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18981 | hp1 | a0002 | c0006 | t0010 | g0023 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18982 | hp1 | a0012 | c0014 | t0004 | g0003 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18982 | hp2 | a0005 | c0005 | t0005 | g0009 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18984 | hp2 | a0002 | c0002 | t0015 | g0005 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18998 | hp1 | a0005 | c0005 | t0005 | g0009 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19002 | hp1 | a0012 | c0014 | t0004 | g0171 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19002 | hp2 | a0002 | c0017 | t0002 | g0019 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19003 | hp1 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19004 | hp1 | a0011 | c0011 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | LWK | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19043 | hp2 | a0006 | c0012 | t0016 | g0098 | AFR | LWK | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19054 | hp1 | a0002 | c0006 | t0002 | g0069 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19060 | hp2 | a0002 | c0006 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19066 | hp1 | a0011 | c0011 | t0002 | g0002 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19077 | hp1 | a0013 | c0022 | t0001 | g0105 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19079 | hp1 | a0004 | c0004 | t0024 | g0056 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19080 | hp1 | a0005 | c0005 | t0005 | g0043 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19081 | hp2 | a0002 | c0006 | t0010 | g0023 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19084 | hp1 | a0005 | c0005 | t0005 | g0009 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19086 | hp2 | a0003 | c0003 | t0021 | g0013 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0138 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20129 | hp1 | a0001 | c0001 | t0023 | g0200 | AFR | ASW | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20129 | hp2 | a0007 | c0013 | t0009 | g0094 | AFR | ASW | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0207 | EUR | TSI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | TSI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0189 | EUR | TSI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0128 | EUR | TSI | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0142 | SAS | GIH | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA20905 | hp2 | a0009 | c0009 | t0001 | g0116 | SAS | GIH | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG01123 | hp2 | a0004 | c0004 | t0006 | g0054 | AMR | CLM | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | ACB | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03471 | hp1 | a0010 | c0025 | t0012 | g0100 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | LWK | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0110 | AFR | LWK | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0119 | REF | REF | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0130 | REF | REF | CPEB2_chr4_14997481_15075151 | CPEB2 | chr4 | 14997481 | 15075151 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15002875 | C | T | 1 | a0004 | 14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
missense_variant | MODERATE | c.202C>T | p.Pro68Ser | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 395/7069 | 202/3105 | 68/1034 | chr4 | 15002875 | |||
| chr4:15003031 | G | A | 16 | a0001 a0002 a0004 others(13): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
missense_variant | MODERATE | c.358G>A | p.Asp120Asn | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 551/7069 | 358/3105 | 120/1034 | chr4 | 15003031 | |||
| chr4:15003247 | G | C | 1 | a0005 | 13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
missense_variant | MODERATE | c.574G>C | p.Asp192His | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 767/7069 | 574/3105 | 192/1034 | chr4 | 15003247 | |||
| chr4:15003254 | A | AGCC | 1 | a0013 | 3 | HG01891.hp1 HG02723.hp1 NA19077.hp1 |
disruptive_inframe_insertion | MODERATE | c.594_596dupGCC | p.Pro199dup | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 790/7069 | 597/3105 | 199/1034 | INFO_REALIGN_3_PRIME | chr4 | 15003254 | ||
| chr4:15003254 | A | AGCCGCC | 3 | a0002 a0011 a0016 |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
disruptive_inframe_insertion | MODERATE | c.591_596dupGCCGCC | p.Pro198_Pro199dup | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 790/7069 | 597/3105 | 199/1034 | INFO_REALIGN_3_PRIME | chr4 | 15003254 | ||
| chr4:15003300 | C | CCCG | 3 | a0002 a0011 a0016 |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
disruptive_inframe_insertion | MODERATE | c.639_641dupGCC | p.Pro214dup | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 835/7069 | 642/3105 | 214/1034 | INFO_REALIGN_3_PRIME | chr4 | 15003300 | ||
| chr4:15003317 | C | A | 1 | a0019 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.644C>A | p.Ala215Asp | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 837/7069 | 644/3105 | 215/1034 | chr4 | 15003317 | |||
| chr4:15003335 | C | A | 4 | a0006 a0010 a0018 others(1): Show |
21 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
missense_variant | MODERATE | c.662C>A | p.Pro221Gln | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 855/7069 | 662/3105 | 221/1034 | chr4 | 15003335 | |||
| chr4:15003604 | C | G | 1 | a0002 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.931C>G | p.Pro311Ala | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1124/7069 | 931/3105 | 311/1034 | chr4 | 15003604 | |||
| chr4:15003704 | GCCCGGAC others(8): Show |
G | 1 | a0012 | 5 | HG01433.hp2 HG02523.hp1 NA18972.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.1037_1051delACCTTC others(9): Show |
p.Asp346_Pro350del | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1230/7069 | 1037/3105 | 346/1034 | INFO_REALIGN_3_PRIME | chr4 | 15003704 | ||
| chr4:15003723 | G | GGGC | 2 | a0011 a0014 |
7 | HG00673.hp1 HG02622.hp2 NA18962.hp2 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.1068_1070dupCGG | p.Gly357dup | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1264/7069 | 1071/3105 | 357/1034 | INFO_REALIGN_3_PRIME | chr4 | 15003723 | ||
| chr4:15003730 | G | T | 1 | a0016 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1057G>T | p.Gly353Cys | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1250/7069 | 1057/3105 | 353/1034 | chr4 | 15003730 | |||
| chr4:15003784 | G | A | 2 | a0008 a0017 |
8 | HG00140.hp2 HG00733.hp2 HG00738.hp1 others(5): Show |
missense_variant | MODERATE | c.1111G>A | p.Ala371Thr | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1304/7069 | 1111/3105 | 371/1034 | chr4 | 15003784 | |||
| chr4:15003812 | G | C | 1 | a0009 | 7 | HG00735.hp1 HG01256.hp2 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.1139G>C | p.Gly380Ala | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1332/7069 | 1139/3105 | 380/1034 | chr4 | 15003812 | |||
| chr4:15003980 | G | A | 5 | a0001 a0012 a0013 others(2): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
missense_variant | MODERATE | c.1307G>A | p.Ser436Asn | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1500/7069 | 1307/3105 | 436/1034 | chr4 | 15003980 | |||
| chr4:15004114 | A | AGCG | 1 | a0005 | 13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
conservative_inframe_insertion | MODERATE | c.1459_1461dupGGC | p.Gly487dup | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1655/7069 | 1462/3105 | 488/1034 | INFO_REALIGN_3_PRIME | chr4 | 15004114 | ||
| chr4:15004214 | C | T | 2 | a0010 a0019 |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
missense_variant | MODERATE | c.1541C>T | p.Pro514Leu | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1734/7069 | 1541/3105 | 514/1034 | chr4 | 15004214 | |||
| chr4:15007404 | A | T | 1 | a0018 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.1762A>T | p.Thr588Ser | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/12 | 1955/7069 | 1762/3105 | 588/1034 | chr4 | 15007404 | |||
| chr4:15017239 | C | G | 1 | a0015 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2086C>G | p.Leu696Val | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/12 | 2279/7069 | 2086/3105 | 696/1034 | chr4 | 15017239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15002775 | G | A | 1 | a0002c0015 | 3 | HG00408.hp2 HG02056.hp1 NA18972.hp1 |
synonymous_variant | LOW | c.102G>A | p.Gly34Gly | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 295/7069 | 102/3105 | 34/1034 | chr4 | 15002775 | |||
| chr4:15003009 | G | T | 1 | a0007c0016 | 3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.336G>T | p.Ala112Ala | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 529/7069 | 336/3105 | 112/1034 | chr4 | 15003009 | |||
| chr4:15003105 | G | A | 1 | a0002c0017 | 2 | NA18979.hp1 NA19002.hp2 |
synonymous_variant | LOW | c.432G>A | p.Leu144Leu | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 625/7069 | 432/3105 | 144/1034 | chr4 | 15003105 | |||
| chr4:15003252 | G | A | 1 | a0004c0004 | 14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
synonymous_variant | LOW | c.579G>A | p.Ser193Ser | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 772/7069 | 579/3105 | 193/1034 | chr4 | 15003252 | |||
| chr4:15003462 | G | A | 1 | a0001c0026 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.789G>A | p.Gln263Gln | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 982/7069 | 789/3105 | 263/1034 | chr4 | 15003462 | |||
| chr4:15003648 | C | A | 1 | a0003c0030 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.975C>A | p.Pro325Pro | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1168/7069 | 975/3105 | 325/1034 | chr4 | 15003648 | |||
| chr4:15003714 | T | C | 1 | a0002c0002 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.1041T>C | p.Leu347Leu | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1234/7069 | 1041/3105 | 347/1034 | chr4 | 15003714 | |||
| chr4:15004017 | C | T | 1 | a0005c0005 | 13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
synonymous_variant | LOW | c.1344C>T | p.Gly448Gly | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 1537/7069 | 1344/3105 | 448/1034 | chr4 | 15004017 | |||
| chr4:15017244 | C | T | 1 | a0001c0028 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.2091C>T | p.Ile697Ile | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/12 | 2284/7069 | 2091/3105 | 697/1034 | chr4 | 15017244 | |||
| chr4:15062107 | G | A | 3 | a0006c0007 a0010c0010 a0019c0023 |
14 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
synonymous_variant | LOW | c.2724G>A | p.Leu908Leu | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/12 | 2917/7069 | 2724/3105 | 908/1034 | chr4 | 15062107 | |||
| chr4:15062206 | T | C | 3 | a0002c0006 a0002c0021 a0011c0011 |
15 | HG00673.hp1 HG03834.hp1 HG03942.hp2 others(12): Show |
synonymous_variant | LOW | c.2823T>C | p.Ile941Ile | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/12 | 3016/7069 | 2823/3105 | 941/1034 | chr4 | 15062206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15002484 | A | G | 1 | a0006c0007t0026 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 190 | chr4 | 15002484 | ||||||
| chr4:15002486 | G | A | 1 | a0005c0005t0005 | 13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | 188 | chr4 | 15002486 | ||||||
| chr4:15002594 | C | T | 1 | a0007c0013t0009 | 5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/12 | chr4 | 15002594 | |||||||
| chr4:15067039 | A | T | 1 | a0001c0001t0025 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*659A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 659 | chr4 | 15067039 | ||||||
| chr4:15067246 | AAAG | A | 2 | a0004c0004t0006 a0004c0004t0024 |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*867_*869delAAG | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 867 | chr4 | 15067246 | ||||||
| chr4:15067603 | A | G | 1 | a0001c0001t0023 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1223A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1223 | chr4 | 15067603 | ||||||
| chr4:15067860 | T | C | 1 | a0009c0009t0011 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1480T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1480 | chr4 | 15067860 | ||||||
| chr4:15067908 | G | A | 4 | a0006c0007t0013 a0010c0010t0007 a0010c0025t0012 others(1): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1528G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1528 | chr4 | 15067908 | ||||||
| chr4:15067962 | A | T | 4 | a0001c0001t0004 a0001c0001t0022 a0001c0028t0004 others(1): Show |
46 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1582A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1582 | chr4 | 15067962 | ||||||
| chr4:15067965 | G | A | 11 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0014 others(8): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1585G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1585 | chr4 | 15067965 | ||||||
| chr4:15068164 | C | G | 1 | a0003c0003t0021 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1784C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 1784 | chr4 | 15068164 | ||||||
| chr4:15068586 | A | G | 1 | a0002c0002t0020 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2206 | chr4 | 15068586 | ||||||
| chr4:15068632 | T | C | 1 | a0002c0002t0014 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2252T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2252 | chr4 | 15068632 | ||||||
| chr4:15068793 | C | T | 1 | a0002c0006t0010 | 2 | NA18981.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2413C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2413 | chr4 | 15068793 | ||||||
| chr4:15068906 | CTTTTG | C | 1 | a0006c0007t0008 | 5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2541_*2545delGTTT others(1): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2541 | INFO_REALIGN_3_PRIME | chr4 | 15068906 | |||||
| chr4:15068979 | G | GT | 9 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0019 others(6): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2608dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2609 | INFO_REALIGN_3_PRIME | chr4 | 15068979 | |||||
| chr4:15068979 | GTTTTT | G | 2 | a0010c0010t0007 a0019c0023t0007 |
7 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2604_*2608delTTTT others(1): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2604 | INFO_REALIGN_3_PRIME | chr4 | 15068979 | |||||
| chr4:15068980 | T | G | 1 | a0002c0002t0015 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2600T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2600 | chr4 | 15068980 | ||||||
| chr4:15069008 | T | C | 1 | a0001c0001t0018 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2628T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2628 | chr4 | 15069008 | ||||||
| chr4:15069095 | T | C | 1 | a0006c0012t0016 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2715 | chr4 | 15069095 | ||||||
| chr4:15069128 | A | T | 1 | a0003c0003t0017 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2748A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 2748 | chr4 | 15069128 | ||||||
| chr4:15069690 | T | C | 1 | a0001c0001t0019 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3310T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 3310 | chr4 | 15069690 | ||||||
| chr4:15069768 | C | A | 1 | a0001c0001t0022 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3388C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 3388 | chr4 | 15069768 | ||||||
| chr4:15069828 | G | T | 1 | a0004c0004t0024 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3448G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 3448 | chr4 | 15069828 | ||||||
| chr4:15069936 | TTATGGAC others(6): Show |
T | 1 | a0010c0025t0012 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3559_*3571delTGGA others(9): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 12/12 | 3559 | INFO_REALIGN_3_PRIME | chr4 | 15069936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15004479 | T | TGA | 90 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(87): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1662+146_1662+147d others(4): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 15004479 | ||||||
| chr4:15004554 | G | C | 11 | a0002c0002t0002g0036 a0005c0005t0005g0009 a0005c0005t0005g0016 others(8): Show |
14 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662+219G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004554 | |||||||
| chr4:15004560 | G | C | 11 | a0002c0002t0002g0036 a0005c0005t0005g0009 a0005c0005t0005g0016 others(8): Show |
14 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662+225G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004560 | |||||||
| chr4:15004597 | C | T | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1662+262C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004597 | |||||||
| chr4:15004842 | C | T | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1662+507C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004842 | |||||||
| chr4:15004918 | C | T | 1 | a0003c0003t0001g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1662+583C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004918 | |||||||
| chr4:15004926 | CT | C | 80 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(77): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1662+601delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 15004926 | ||||||
| chr4:15004927 | T | G | 1 | a0004c0004t0006g0045 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1662+592T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004927 | |||||||
| chr4:15004980 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1662+645C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15004980 | |||||||
| chr4:15005113 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0013c0018t0001g0106 others(2): Show |
6 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1662+778G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005113 | |||||||
| chr4:15005183 | C | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1662+848C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005183 | |||||||
| chr4:15005396 | G | A | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1662+1061G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005396 | |||||||
| chr4:15005400 | C | T | 22 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(19): Show |
26 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1662+1065C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005400 | |||||||
| chr4:15005458 | C | T | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1662+1123C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005458 | |||||||
| chr4:15005509 | G | C | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1662+1174G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005509 | |||||||
| chr4:15005995 | C | T | 40 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(37): Show |
58 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1663-1310C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15005995 | |||||||
| chr4:15006001 | T | A | 1 | a0018c0024t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1663-1304T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006001 | |||||||
| chr4:15006014 | A | C | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1663-1291A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006014 | |||||||
| chr4:15006061 | AT | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(78): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1663-1243delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006061 | |||||||
| chr4:15006091 | T | G | 52 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(49): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1663-1214T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006091 | |||||||
| chr4:15006343 | C | A | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1663-962C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006343 | |||||||
| chr4:15006364 | A | G | 7 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0201 others(4): Show |
11 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1663-941A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006364 | |||||||
| chr4:15006419 | T | TAA | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1663-873_1663-872d others(4): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 15006419 | ||||||
| chr4:15006433 | A | AC | 12 | a0002c0002t0002g0036 a0002c0002t0020g0049 a0005c0005t0005g0009 others(9): Show |
15 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.1663-869dupC | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 15006433 | ||||||
| chr4:15006433 | A | C | 40 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(37): Show |
58 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1663-872A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006433 | |||||||
| chr4:15006602 | A | G | 52 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0020 others(49): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1663-703A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006602 | |||||||
| chr4:15006923 | G | A | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1663-382G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15006923 | |||||||
| chr4:15007168 | T | G | 1 | a0002c0002t0002g0059 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1663-137T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15007168 | |||||||
| chr4:15007276 | C | T | 1 | a0014c0019t0001g0109 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1663-29C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15007276 | |||||||
| chr4:15007277 | G | A | 22 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(19): Show |
26 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.1663-28G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 1/11 | chr4 | 15007277 | |||||||
| chr4:15007608 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(84): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1944+22C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007608 | |||||||
| chr4:15007614 | C | T | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1944+28C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007614 | |||||||
| chr4:15007681 | T | C | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1944+95T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007681 | |||||||
| chr4:15007808 | G | T | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1944+222G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007808 | |||||||
| chr4:15007836 | A | G | 1 | a0005c0005t0005g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1944+250A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007836 | |||||||
| chr4:15007840 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(78): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1944+254A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007840 | |||||||
| chr4:15007985 | A | G | 1 | a0001c0001t0023g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1945-353A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15007985 | |||||||
| chr4:15008157 | A | G | 1 | a0001c0001t0004g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1945-181A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 2/11 | chr4 | 15008157 | |||||||
| chr4:15008489 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
5 | HG01123.hp1 HG01169.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2034+62G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15008489 | |||||||
| chr4:15008966 | A | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(83): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2034+539A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15008966 | |||||||
| chr4:15009117 | T | C | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034+690T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009117 | |||||||
| chr4:15009221 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2034+794A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009221 | |||||||
| chr4:15009290 | A | G | 1 | a0001c0001t0004g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2034+863A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009290 | |||||||
| chr4:15009302 | C | T | 1 | a0007c0013t0009g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2034+875C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009302 | |||||||
| chr4:15009502 | A | C | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034+1075A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009502 | |||||||
| chr4:15009602 | G | C | 1 | a0003c0003t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2034+1175G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009602 | |||||||
| chr4:15009786 | A | G | 1 | a0001c0001t0003g0198 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2034+1359A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009786 | |||||||
| chr4:15009884 | C | T | 11 | a0002c0002t0020g0049 a0005c0005t0005g0009 a0005c0005t0005g0016 others(8): Show |
14 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034+1457C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15009884 | |||||||
| chr4:15010791 | G | A | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2034+2364G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15010791 | |||||||
| chr4:15010853 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0014c0019t0001g0109 |
4 | HG02559.hp1 HG02622.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2034+2426C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15010853 | |||||||
| chr4:15010984 | A | T | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034+2557A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15010984 | |||||||
| chr4:15011101 | C | CT | 18 | a0001c0001t0003g0197 a0005c0005t0005g0009 a0005c0005t0005g0016 others(15): Show |
21 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(18): Show |
intron_variant | MODIFIER | c.2034+2693dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15011101 | ||||||
| chr4:15011101 | C | CTT | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034+2692_2034+269 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15011101 | ||||||
| chr4:15011101 | CT | C | 7 | a0001c0001t0001g0035 a0001c0001t0003g0150 a0001c0001t0004g0149 others(4): Show |
8 | HG00639.hp2 HG01069.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2034+2693delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15011101 | ||||||
| chr4:15011106 | T | C | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2034+2679T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011106 | |||||||
| chr4:15011108 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2034+2681T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011108 | |||||||
| chr4:15011140 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2034+2713A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011140 | |||||||
| chr4:15011188 | C | T | 1 | a0001c0001t0022g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2034+2761C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011188 | |||||||
| chr4:15011246 | A | G | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2034+2819A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011246 | |||||||
| chr4:15011399 | C | T | 1 | a0006c0007t0008g0092 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2034+2972C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011399 | |||||||
| chr4:15011524 | C | G | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2034+3097C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011524 | |||||||
| chr4:15011675 | C | T | 1 | a0007c0013t0009g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2034+3248C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011675 | |||||||
| chr4:15011700 | A | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2034+3273A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011700 | |||||||
| chr4:15011737 | A | C | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2034+3310A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011737 | |||||||
| chr4:15011830 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2034+3403C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011830 | |||||||
| chr4:15011920 | A | G | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2034+3493A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011920 | |||||||
| chr4:15011944 | G | C | 4 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2034+3517G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15011944 | |||||||
| chr4:15011969 | T | TAGTC | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2034+3544_2034+354 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15011969 | ||||||
| chr4:15012076 | A | G | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2034+3649A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012076 | |||||||
| chr4:15012272 | T | G | 1 | a0002c0002t0002g0061 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2034+3845T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012272 | |||||||
| chr4:15012350 | AT | A | 53 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(50): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2034+3931delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15012350 | ||||||
| chr4:15012390 | C | T | 1 | a0013c0018t0001g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2034+3963C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012390 | |||||||
| chr4:15012696 | A | G | 2 | a0005c0005t0005g0009 a0005c0005t0005g0043 |
4 | NA18982.hp2 NA18998.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+4269A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012696 | |||||||
| chr4:15012737 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2034+4310G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012737 | |||||||
| chr4:15012883 | A | G | 1 | a0002c0002t0002g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2035-4305A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012883 | |||||||
| chr4:15012947 | T | C | 1 | a0002c0015t0002g0062 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2035-4241T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15012947 | |||||||
| chr4:15013142 | TGTAA | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035-4043_2035-404 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15013142 | ||||||
| chr4:15013256 | A | T | 1 | a0001c0001t0003g0195 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2035-3932A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013256 | |||||||
| chr4:15013289 | C | A | 2 | a0004c0004t0006g0050 a0004c0004t0006g0051 |
2 | HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2035-3899C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013289 | |||||||
| chr4:15013362 | C | T | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2035-3826C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013362 | |||||||
| chr4:15013372 | T | C | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2035-3816T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013372 | |||||||
| chr4:15013402 | A | G | 55 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(52): Show |
76 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.2035-3786A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013402 | |||||||
| chr4:15013788 | A | G | 1 | a0004c0004t0006g0058 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2035-3400A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013788 | |||||||
| chr4:15013968 | C | T | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2035-3220C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15013968 | |||||||
| chr4:15014020 | A | G | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2035-3168A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014020 | |||||||
| chr4:15014148 | C | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2035-3040C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014148 | |||||||
| chr4:15014346 | G | T | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2035-2842G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014346 | |||||||
| chr4:15014389 | A | AT | 43 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(40): Show |
61 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2035-2793dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 15014389 | ||||||
| chr4:15014576 | A | T | 1 | a0003c0030t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2035-2612A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014576 | |||||||
| chr4:15014832 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2035-2356A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014832 | |||||||
| chr4:15014841 | G | A | 1 | a0001c0001t0004g0152 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2035-2347G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014841 | |||||||
| chr4:15014969 | C | G | 2 | a0003c0003t0001g0141 a0003c0003t0001g0142 |
2 | HG00639.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2035-2219C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15014969 | |||||||
| chr4:15015076 | C | T | 1 | a0002c0002t0002g0063 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2035-2112C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015076 | |||||||
| chr4:15015445 | C | T | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2035-1743C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015445 | |||||||
| chr4:15015517 | C | T | 43 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(40): Show |
61 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2035-1671C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015517 | |||||||
| chr4:15015572 | T | A | 1 | a0001c0001t0004g0152 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2035-1616T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015572 | |||||||
| chr4:15015684 | C | T | 2 | a0003c0003t0001g0141 a0003c0003t0001g0142 |
2 | HG00639.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2035-1504C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015684 | |||||||
| chr4:15015711 | G | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035-1477G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015711 | |||||||
| chr4:15015714 | C | T | 53 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(50): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2035-1474C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015714 | |||||||
| chr4:15015792 | A | G | 1 | a0002c0006t0010g0023 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2035-1396A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15015792 | |||||||
| chr4:15016010 | A | T | 1 | a0003c0003t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2035-1178A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016010 | |||||||
| chr4:15016057 | C | T | 1 | a0018c0024t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2035-1131C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016057 | |||||||
| chr4:15016077 | A | C | 1 | a0015c0029t0003g0194 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2035-1111A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016077 | |||||||
| chr4:15016229 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2035-959G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016229 | |||||||
| chr4:15016379 | T | C | 53 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(50): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2035-809T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016379 | |||||||
| chr4:15016408 | A | G | 2 | a0001c0001t0003g0193 a0002c0002t0002g0022 |
3 | NA18990.hp2 NA19056.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2035-780A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016408 | |||||||
| chr4:15016542 | G | C | 2 | a0001c0001t0001g0035 a0006c0007t0026g0090 |
3 | HG02647.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2035-646G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016542 | |||||||
| chr4:15016555 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0154 |
4 | HG02145.hp2 HG03704.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2035-633G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016555 | |||||||
| chr4:15016556 | G | A | 1 | a0003c0003t0001g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2035-632G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016556 | |||||||
| chr4:15016628 | A | G | 1 | a0005c0005t0005g0042 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2035-560A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016628 | |||||||
| chr4:15016678 | A | G | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035-510A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016678 | |||||||
| chr4:15016696 | C | T | 1 | a0002c0002t0002g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2035-492C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016696 | |||||||
| chr4:15016800 | T | C | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035-388T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016800 | |||||||
| chr4:15016919 | T | C | 1 | a0001c0001t0003g0155 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2035-269T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016919 | |||||||
| chr4:15016970 | A | G | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2035-218A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15016970 | |||||||
| chr4:15017012 | A | G | 1 | a0007c0016t0001g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2035-176A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15017012 | |||||||
| chr4:15017135 | C | T | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2035-53C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 3/11 | chr4 | 15017135 | |||||||
| chr4:15017303 | A | T | 4 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125+25A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15017303 | |||||||
| chr4:15017666 | C | T | 1 | a0003c0003t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2125+388C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15017666 | |||||||
| chr4:15017711 | G | C | 1 | a0002c0002t0002g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2125+433G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15017711 | |||||||
| chr4:15017831 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2125+553G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15017831 | |||||||
| chr4:15017962 | T | A | 1 | a0004c0004t0006g0050 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2125+684T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15017962 | |||||||
| chr4:15018174 | G | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2125+896G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018174 | |||||||
| chr4:15018304 | A | G | 7 | a0010c0010t0007g0011 a0010c0010t0007g0101 a0010c0010t0007g0102 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125+1026A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018304 | |||||||
| chr4:15018317 | T | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2125+1039T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018317 | |||||||
| chr4:15018341 | T | G | 1 | a0001c0026t0001g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2125+1063T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018341 | |||||||
| chr4:15018520 | A | G | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2125+1242A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018520 | |||||||
| chr4:15018602 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2125+1324A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018602 | |||||||
| chr4:15018720 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2125+1442T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018720 | |||||||
| chr4:15018762 | T | G | 1 | a0001c0001t0003g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2125+1484T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018762 | |||||||
| chr4:15018936 | T | TTA | 5 | a0003c0003t0001g0110 a0003c0003t0001g0131 a0003c0003t0001g0142 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+1691_2125+169 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | T | TTATA | 4 | a0003c0003t0001g0113 a0003c0003t0001g0135 a0008c0008t0001g0112 others(1): Show |
4 | HG00733.hp2 HG01069.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125+1689_2125+169 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | T | TTATATA | 3 | a0003c0003t0001g0136 a0003c0003t0001g0137 a0003c0030t0001g0143 |
3 | HG02970.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2125+1687_2125+169 others(10): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | T | TTATATAT others(5): Show |
1 | a0003c0003t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2125+1681_2125+169 others(16): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | T | TTATATAT others(7): Show |
1 | a0003c0003t0001g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2125+1679_2125+169 others(18): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTA | T | 9 | a0002c0002t0002g0080 a0002c0002t0002g0081 a0002c0002t0002g0082 others(6): Show |
11 | HG02257.hp1 HG02258.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.2125+1691_2125+169 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTATA | T | 13 | a0002c0002t0002g0006 a0002c0002t0002g0020 a0002c0002t0002g0064 others(10): Show |
18 | HG00621.hp2 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2125+1689_2125+169 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTATATA | T | 43 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0108 others(40): Show |
60 | HG00408.hp2 HG00673.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.2125+1687_2125+169 others(10): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTATATAT others(1): Show |
T | 11 | a0001c0001t0001g0160 a0001c0001t0003g0150 a0002c0002t0002g0067 others(8): Show |
13 | HG01106.hp1 HG02523.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125+1685_2125+169 others(12): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTATATAT others(3): Show |
T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0153 a0001c0001t0001g0154 others(73): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2125+1683_2125+169 others(14): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018936 | TTATATAT others(5): Show |
T | 11 | a0001c0001t0001g0031 a0005c0005t0005g0009 a0005c0005t0005g0016 others(8): Show |
15 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.2125+1681_2125+169 others(16): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018936 | ||||||
| chr4:15018967 | T | C | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2125+1689T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018967 | |||||||
| chr4:15018969 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(125): Show |
179 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.2125+1691T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15018969 | |||||||
| chr4:15018969 | T | TATATAC | 5 | a0004c0004t0006g0017 a0004c0004t0006g0053 a0004c0004t0006g0054 others(2): Show |
6 | HG00423.hp2 HG01081.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.2125+1692_2125+169 others(10): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018969 | ||||||
| chr4:15018969 | T | TATATATA others(1): Show |
2 | a0004c0004t0006g0018 a0004c0004t0006g0050 |
3 | HG03017.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2125+1692_2125+169 others(12): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018969 | ||||||
| chr4:15018969 | T | TATATATA others(3): Show |
2 | a0004c0004t0006g0045 a0004c0004t0024g0056 |
2 | NA18980.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2125+1692_2125+169 others(14): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018969 | ||||||
| chr4:15018969 | T | TATATATA others(7): Show |
1 | a0004c0004t0006g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2125+1692_2125+169 others(18): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018969 | ||||||
| chr4:15018969 | T | TATATATA others(9): Show |
1 | a0004c0004t0006g0051 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2125+1692_2125+169 others(20): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15018969 | ||||||
| chr4:15019160 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(163): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2125+1882G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019160 | |||||||
| chr4:15019293 | A | C | 130 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(127): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.2125+2015A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019293 | |||||||
| chr4:15019308 | A | G | 1 | a0010c0010t0007g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2125+2030A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019308 | |||||||
| chr4:15019448 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2125+2170A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019448 | |||||||
| chr4:15019494 | G | A | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2125+2216G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019494 | |||||||
| chr4:15019561 | T | C | 42 | a0003c0003t0001g0013 a0003c0003t0001g0027 a0003c0003t0001g0029 others(39): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2125+2283T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019561 | |||||||
| chr4:15019826 | A | C | 1 | a0003c0003t0001g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2125+2548A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15019826 | |||||||
| chr4:15020207 | A | G | 1 | a0001c0026t0001g0161 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2125+2929A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020207 | |||||||
| chr4:15020403 | G | GC | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+3126dupC | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15020403 | ||||||
| chr4:15020420 | T | A | 2 | a0003c0003t0001g0117 a0003c0003t0001g0118 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2125+3142T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020420 | |||||||
| chr4:15020482 | A | G | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2125+3204A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020482 | |||||||
| chr4:15020653 | A | G | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2125+3375A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020653 | |||||||
| chr4:15020665 | T | A | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2125+3387T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020665 | |||||||
| chr4:15020720 | T | C | 17 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(14): Show |
21 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2125+3442T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020720 | |||||||
| chr4:15020737 | T | C | 1 | a0003c0003t0017g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2125+3459T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020737 | |||||||
| chr4:15020752 | G | A | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2125+3474G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020752 | |||||||
| chr4:15020767 | A | G | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2125+3489A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15020767 | |||||||
| chr4:15021220 | T | C | 1 | a0002c0006t0002g0069 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2125+3942T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15021220 | |||||||
| chr4:15021483 | C | T | 1 | a0001c0001t0003g0146 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2125+4205C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15021483 | |||||||
| chr4:15021574 | G | C | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2125+4296G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15021574 | |||||||
| chr4:15021671 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(173): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2125+4393G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15021671 | |||||||
| chr4:15021890 | C | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(163): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2125+4612C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15021890 | |||||||
| chr4:15022088 | C | A | 1 | a0003c0003t0001g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2125+4810C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022088 | |||||||
| chr4:15022116 | A | T | 1 | a0014c0019t0003g0192 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2125+4838A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022116 | |||||||
| chr4:15022142 | G | A | 2 | a0005c0005t0005g0037 a0005c0005t0005g0038 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2125+4864G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022142 | |||||||
| chr4:15022245 | A | G | 3 | a0003c0003t0001g0029 a0003c0003t0001g0128 a0003c0003t0001g0135 |
4 | HG02698.hp1 HG03927.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+4967A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022245 | |||||||
| chr4:15022263 | TA | T | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2125+4989delA | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15022263 | ||||||
| chr4:15022450 | A | G | 4 | a0005c0005t0005g0037 a0005c0005t0005g0038 a0005c0005t0005g0040 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125+5172A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022450 | |||||||
| chr4:15022587 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(83): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2125+5309T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022587 | |||||||
| chr4:15022757 | G | C | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2125+5479G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022757 | |||||||
| chr4:15022892 | T | C | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2125+5614T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15022892 | |||||||
| chr4:15023151 | C | G | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2125+5873C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023151 | |||||||
| chr4:15023316 | A | G | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2125+6038A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023316 | |||||||
| chr4:15023341 | G | GT | 2 | a0006c0007t0008g0024 a0006c0007t0008g0089 |
3 | HG02257.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2125+6069dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15023341 | ||||||
| chr4:15023633 | T | C | 2 | a0003c0003t0001g0117 a0003c0003t0001g0118 |
2 | HG01081.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2125+6355T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023633 | |||||||
| chr4:15023864 | A | G | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2125+6586A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023864 | |||||||
| chr4:15023961 | C | T | 2 | a0006c0007t0008g0024 a0006c0007t0008g0089 |
3 | HG02257.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2125+6683C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023961 | |||||||
| chr4:15023975 | T | A | 1 | a0002c0017t0002g0019 | 2 | NA18979.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2125+6697T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023975 | |||||||
| chr4:15023994 | C | G | 42 | a0003c0003t0001g0013 a0003c0003t0001g0027 a0003c0003t0001g0029 others(39): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2125+6716C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15023994 | |||||||
| chr4:15024132 | G | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+6854G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024132 | |||||||
| chr4:15024137 | A | G | 1 | a0001c0001t0004g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2125+6859A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024137 | |||||||
| chr4:15024398 | G | A | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2125+7120G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024398 | |||||||
| chr4:15024413 | A | C | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2125+7135A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024413 | |||||||
| chr4:15024554 | T | A | 218 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(215): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2125+7276T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024554 | |||||||
| chr4:15024588 | G | A | 218 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(215): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2125+7310G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024588 | |||||||
| chr4:15024644 | T | C | 22 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(19): Show |
27 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.2125+7366T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024644 | |||||||
| chr4:15024669 | C | T | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2125+7391C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024669 | |||||||
| chr4:15024721 | T | A | 1 | a0001c0001t0004g0152 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2125+7443T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024721 | |||||||
| chr4:15024743 | AT | A | 136 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0035 others(133): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2125+7484delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15024743 | ||||||
| chr4:15024743 | ATT | A | 53 | a0001c0001t0001g0108 a0001c0001t0001g0156 a0001c0001t0002g0147 others(50): Show |
71 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.2125+7483_2125+748 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15024743 | ||||||
| chr4:15024743 | ATTT | A | 11 | a0001c0001t0001g0025 a0005c0005t0005g0009 a0005c0005t0005g0016 others(8): Show |
15 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.2125+7482_2125+748 others(7): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15024743 | ||||||
| chr4:15024743 | ATTTT | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2125+7481_2125+748 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15024743 | ||||||
| chr4:15024777 | G | C | 1 | a0003c0003t0001g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2125+7499G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024777 | |||||||
| chr4:15024802 | G | A | 218 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(215): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2125+7524G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024802 | |||||||
| chr4:15024865 | C | T | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+7587C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024865 | |||||||
| chr4:15024894 | C | T | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2125+7616C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15024894 | |||||||
| chr4:15025471 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2126-7690T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025471 | |||||||
| chr4:15025529 | C | T | 1 | a0004c0004t0006g0051 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2126-7632C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025529 | |||||||
| chr4:15025568 | C | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(151): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2126-7593C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025568 | |||||||
| chr4:15025740 | T | C | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2126-7421T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025740 | |||||||
| chr4:15025808 | A | AC | 215 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(212): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2126-7352dupC | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15025808 | ||||||
| chr4:15025809 | C | CT | 3 | a0004c0004t0006g0018 a0004c0004t0006g0054 a0004c0004t0006g0055 |
4 | HG01081.hp1 HG01123.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-7352_2126-735 others(5): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025809 | |||||||
| chr4:15025821 | G | A | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2126-7340G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025821 | |||||||
| chr4:15025872 | A | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2126-7289A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15025872 | |||||||
| chr4:15026009 | C | T | 3 | a0001c0001t0003g0186 a0001c0001t0004g0199 a0005c0005t0005g0041 |
3 | HG02630.hp1 NA18963.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2126-7152C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026009 | |||||||
| chr4:15026010 | G | A | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2126-7151G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026010 | |||||||
| chr4:15026232 | G | GT | 9 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(6): Show |
12 | HG02257.hp1 HG02258.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2126-6924dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15026232 | ||||||
| chr4:15026238 | G | T | 214 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(211): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.2126-6923G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026238 | |||||||
| chr4:15026250 | G | A | 22 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(19): Show |
26 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.2126-6911G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026250 | |||||||
| chr4:15026251 | G | T | 1 | a0003c0003t0001g0127 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2126-6910G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026251 | |||||||
| chr4:15026419 | G | C | 42 | a0003c0003t0001g0013 a0003c0003t0001g0027 a0003c0003t0001g0029 others(39): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2126-6742G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026419 | |||||||
| chr4:15026446 | T | C | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2126-6715T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026446 | |||||||
| chr4:15026473 | G | A | 1 | a0006c0012t0001g0010 | 3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2126-6688G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026473 | |||||||
| chr4:15026528 | A | G | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2126-6633A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026528 | |||||||
| chr4:15026638 | A | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2126-6523A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026638 | |||||||
| chr4:15026756 | A | G | 2 | a0007c0016t0001g0047 a0007c0016t0001g0048 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2126-6405A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026756 | |||||||
| chr4:15026783 | G | A | 1 | a0003c0003t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2126-6378G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026783 | |||||||
| chr4:15026926 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2126-6235A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15026926 | |||||||
| chr4:15027198 | G | A | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2126-5963G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15027198 | |||||||
| chr4:15027312 | A | G | 1 | a0002c0002t0014g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2126-5849A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15027312 | |||||||
| chr4:15027384 | CGGATCTG others(7): Show |
C | 3 | a0002c0002t0002g0006 a0002c0002t0002g0070 a0002c0002t0002g0071 |
6 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2126-5770_2126-575 others(18): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15027384 | ||||||
| chr4:15027473 | G | A | 1 | a0002c0006t0010g0023 | 2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2126-5688G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15027473 | |||||||
| chr4:15027980 | C | G | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2126-5181C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15027980 | |||||||
| chr4:15028099 | A | G | 1 | a0001c0001t0004g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-5062A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028099 | |||||||
| chr4:15028179 | C | T | 176 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(173): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2126-4982C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028179 | |||||||
| chr4:15028328 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2126-4833T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028328 | |||||||
| chr4:15028330 | A | AT | 43 | a0001c0001t0001g0035 a0001c0001t0004g0184 a0003c0003t0001g0013 others(40): Show |
49 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2126-4820dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15028330 | ||||||
| chr4:15028330 | AT | A | 7 | a0001c0001t0004g0163 a0007c0013t0009g0091 a0007c0013t0009g0093 others(4): Show |
7 | HG01891.hp1 HG02818.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-4820delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15028330 | ||||||
| chr4:15028490 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2126-4671G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028490 | |||||||
| chr4:15028604 | A | C | 4 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2126-4557A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028604 | |||||||
| chr4:15028663 | C | G | 1 | a0003c0003t0001g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2126-4498C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028663 | |||||||
| chr4:15028872 | C | G | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2126-4289C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028872 | |||||||
| chr4:15028900 | G | A | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2126-4261G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028900 | |||||||
| chr4:15028942 | A | C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2126-4219A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028942 | |||||||
| chr4:15028978 | T | C | 1 | a0002c0002t0002g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2126-4183T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028978 | |||||||
| chr4:15028999 | G | A | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2126-4162G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15028999 | |||||||
| chr4:15029040 | G | A | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2126-4121G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029040 | |||||||
| chr4:15029057 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2126-4104A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029057 | |||||||
| chr4:15029161 | C | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-4000C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029161 | |||||||
| chr4:15029430 | A | G | 1 | a0001c0001t0003g0015 | 3 | HG02735.hp1 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2126-3731A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029430 | |||||||
| chr4:15029488 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2126-3673C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029488 | |||||||
| chr4:15029493 | C | G | 1 | a0002c0002t0002g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2126-3668C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029493 | |||||||
| chr4:15029769 | T | C | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2126-3392T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029769 | |||||||
| chr4:15029773 | A | G | 147 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(144): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2126-3388A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029773 | |||||||
| chr4:15029954 | G | T | 1 | a0003c0003t0001g0128 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2126-3207G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029954 | |||||||
| chr4:15029974 | A | G | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-3187A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15029974 | |||||||
| chr4:15030018 | T | C | 1 | a0002c0015t0002g0062 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2126-3143T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030018 | |||||||
| chr4:15030157 | G | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0108 others(3): Show |
8 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2126-3004G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030157 | |||||||
| chr4:15030302 | G | A | 1 | a0001c0001t0004g0164 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2126-2859G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030302 | |||||||
| chr4:15030309 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0154 |
4 | HG02145.hp2 HG03704.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2126-2852A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030309 | |||||||
| chr4:15030547 | G | C | 1 | a0001c0001t0004g0165 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2126-2614G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030547 | |||||||
| chr4:15030632 | C | G | 1 | a0007c0016t0001g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2126-2529C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030632 | |||||||
| chr4:15030799 | T | C | 1 | a0003c0003t0017g0114 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2126-2362T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030799 | |||||||
| chr4:15030842 | A | G | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2126-2319A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030842 | |||||||
| chr4:15030857 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(163): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2126-2304A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030857 | |||||||
| chr4:15030945 | C | T | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-2216C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15030945 | |||||||
| chr4:15031083 | C | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-2078C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031083 | |||||||
| chr4:15031140 | A | G | 1 | a0001c0001t0004g0182 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2126-2021A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031140 | |||||||
| chr4:15031184 | A | G | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2126-1977A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031184 | |||||||
| chr4:15031240 | A | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-1921A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031240 | |||||||
| chr4:15031488 | C | T | 1 | a0009c0009t0001g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2126-1673C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031488 | |||||||
| chr4:15031597 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2126-1564A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031597 | |||||||
| chr4:15031860 | G | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-1301G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031860 | |||||||
| chr4:15031901 | G | GCTTGCTG others(36): Show |
1 | a0006c0007t0008g0089 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2126-1229_2126-118 others(47): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15031901 | ||||||
| chr4:15031929 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2126-1232G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031929 | |||||||
| chr4:15031980 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0013c0018t0001g0106 others(2): Show |
6 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2126-1181G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15031980 | |||||||
| chr4:15032035 | A | T | 2 | a0003c0003t0001g0125 a0003c0003t0001g0127 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2126-1126A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032035 | |||||||
| chr4:15032073 | A | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-1088A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032073 | |||||||
| chr4:15032107 | A | T | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2126-1054A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032107 | |||||||
| chr4:15032182 | C | G | 1 | a0003c0003t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2126-979C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032182 | |||||||
| chr4:15032193 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2126-968G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032193 | |||||||
| chr4:15032222 | C | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-939C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032222 | |||||||
| chr4:15032229 | G | C | 164 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(161): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2126-932G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032229 | |||||||
| chr4:15032427 | T | C | 1 | a0001c0001t0004g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2126-734T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032427 | |||||||
| chr4:15032567 | T | A | 1 | a0001c0001t0003g0187 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2126-594T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032567 | |||||||
| chr4:15032567 | T | TA | 78 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(75): Show |
111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2126-593dupA | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 15032567 | ||||||
| chr4:15032605 | T | C | 1 | a0007c0016t0001g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2126-556T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032605 | |||||||
| chr4:15032682 | C | A | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2126-479C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032682 | |||||||
| chr4:15032740 | T | C | 1 | a0001c0001t0004g0166 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2126-421T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032740 | |||||||
| chr4:15032824 | C | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2126-337C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032824 | |||||||
| chr4:15032848 | A | G | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2126-313A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032848 | |||||||
| chr4:15032852 | G | C | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2126-309G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 4/11 | chr4 | 15032852 | |||||||
| chr4:15033279 | C | G | 3 | a0002c0015t0002g0062 a0002c0015t0002g0078 a0002c0015t0002g0084 |
3 | HG00408.hp2 HG02056.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2176+68C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033279 | |||||||
| chr4:15033362 | A | G | 1 | a0003c0003t0001g0113 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2176+151A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033362 | |||||||
| chr4:15033668 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2176+457C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033668 | |||||||
| chr4:15033755 | G | A | 2 | a0002c0002t0002g0066 a0002c0002t0002g0072 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2176+544G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033755 | |||||||
| chr4:15033877 | G | C | 1 | a0001c0001t0004g0167 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2176+666G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033877 | |||||||
| chr4:15033932 | AT | A | 41 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(38): Show |
59 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.2176+722delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15033932 | |||||||
| chr4:15034030 | G | A | 1 | a0002c0002t0002g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2176+819G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034030 | |||||||
| chr4:15034133 | T | C | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176+922T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034133 | |||||||
| chr4:15034178 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0013c0018t0001g0106 others(3): Show |
7 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176+967A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034178 | |||||||
| chr4:15034541 | G | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2176+1330G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034541 | |||||||
| chr4:15034603 | T | C | 1 | a0001c0001t0003g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2176+1392T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034603 | |||||||
| chr4:15034644 | A | C | 17 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(14): Show |
21 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2176+1433A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15034644 | |||||||
| chr4:15035048 | G | A | 6 | a0002c0002t0002g0073 a0002c0002t0002g0080 a0002c0002t0002g0081 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2176+1837G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15035048 | |||||||
| chr4:15035211 | C | CT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0108 others(20): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.2176+2009dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15035211 | ||||||
| chr4:15035784 | G | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
5 | HG01123.hp1 HG01169.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176+2573G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15035784 | |||||||
| chr4:15035810 | T | C | 1 | a0001c0001t0003g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2176+2599T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15035810 | |||||||
| chr4:15036016 | A | G | 1 | a0010c0010t0007g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2176+2805A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036016 | |||||||
| chr4:15036126 | T | C | 7 | a0002c0002t0002g0070 a0002c0002t0002g0073 a0002c0002t0002g0080 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176+2915T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036126 | |||||||
| chr4:15036174 | TA | T | 4 | a0005c0005t0005g0037 a0005c0005t0005g0038 a0005c0005t0005g0040 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176+2969delA | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15036174 | ||||||
| chr4:15036203 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(152): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2176+2992T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036203 | |||||||
| chr4:15036221 | G | A | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2176+3010G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036221 | |||||||
| chr4:15036582 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2176+3371T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036582 | |||||||
| chr4:15036608 | G | A | 1 | a0007c0016t0001g0046 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2176+3397G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036608 | |||||||
| chr4:15036650 | C | T | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176+3439C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036650 | |||||||
| chr4:15036715 | G | A | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2176+3504G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036715 | |||||||
| chr4:15036784 | A | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2176+3573A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036784 | |||||||
| chr4:15036787 | T | C | 54 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(51): Show |
74 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.2176+3576T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036787 | |||||||
| chr4:15036964 | G | A | 1 | a0002c0017t0002g0019 | 2 | NA18979.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2177-3500G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15036964 | |||||||
| chr4:15037118 | C | T | 1 | a0003c0003t0001g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2177-3346C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037118 | |||||||
| chr4:15037119 | G | A | 1 | a0002c0002t0002g0074 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2177-3345G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037119 | |||||||
| chr4:15037144 | T | C | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2177-3320T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037144 | |||||||
| chr4:15037227 | C | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2177-3237C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037227 | |||||||
| chr4:15037297 | C | A | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2177-3167C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037297 | |||||||
| chr4:15037310 | C | T | 1 | a0001c0001t0003g0198 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2177-3154C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037310 | |||||||
| chr4:15037327 | G | C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2177-3137G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037327 | |||||||
| chr4:15037615 | A | G | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2177-2849A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037615 | |||||||
| chr4:15037625 | A | G | 1 | a0009c0009t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2177-2839A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037625 | |||||||
| chr4:15037995 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2177-2469T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15037995 | |||||||
| chr4:15038001 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2177-2463A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038001 | |||||||
| chr4:15038041 | T | C | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2177-2423T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038041 | |||||||
| chr4:15038054 | A | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2177-2410A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038054 | |||||||
| chr4:15038352 | CATCATAA others(3): Show |
C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2177-2106_2177-209 others(14): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15038352 | ||||||
| chr4:15038558 | C | CAACT | 28 | a0001c0001t0003g0178 a0001c0001t0004g0001 a0001c0001t0004g0003 others(25): Show |
47 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2177-1904_2177-190 others(8): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15038558 | ||||||
| chr4:15038585 | C | CT | 21 | a0002c0002t0002g0066 a0002c0002t0002g0072 a0002c0002t0002g0086 others(18): Show |
23 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2177-1862dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15038585 | ||||||
| chr4:15038585 | C | CTT | 7 | a0002c0002t0020g0049 a0005c0005t0005g0009 a0005c0005t0005g0016 others(4): Show |
10 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177-1863_2177-186 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15038585 | ||||||
| chr4:15038602 | T | C | 1 | a0001c0001t0003g0173 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2177-1862T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038602 | |||||||
| chr4:15038778 | G | A | 1 | a0002c0002t0014g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2177-1686G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038778 | |||||||
| chr4:15038818 | G | T | 1 | a0001c0001t0003g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2177-1646G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038818 | |||||||
| chr4:15038943 | CA | C | 3 | a0001c0001t0003g0201 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG01074.hp2 HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2177-1520delA | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038943 | |||||||
| chr4:15038957 | T | C | 2 | a0001c0001t0004g0007 a0001c0001t0004g0165 |
5 | NA18942.hp1 NA18943.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.2177-1507T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15038957 | |||||||
| chr4:15039041 | G | C | 1 | a0002c0002t0002g0060 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2177-1423G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039041 | |||||||
| chr4:15039047 | A | G | 67 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(64): Show |
90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2177-1417A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039047 | |||||||
| chr4:15039284 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2177-1180T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039284 | |||||||
| chr4:15039409 | T | G | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2177-1055T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039409 | |||||||
| chr4:15039490 | T | A | 89 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2177-974T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039490 | |||||||
| chr4:15039517 | C | CTTTG | 90 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(87): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2177-939_2177-936d others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr4 | 15039517 | ||||||
| chr4:15039958 | A | G | 2 | a0005c0005t0005g0009 a0005c0005t0005g0043 |
4 | NA18982.hp2 NA18998.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177-506A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15039958 | |||||||
| chr4:15040049 | A | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2177-415A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040049 | |||||||
| chr4:15040053 | A | G | 1 | a0002c0002t0002g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2177-411A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040053 | |||||||
| chr4:15040146 | C | T | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2177-318C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040146 | |||||||
| chr4:15040250 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(40): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.2177-214A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040250 | |||||||
| chr4:15040348 | A | G | 52 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(49): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2177-116A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040348 | |||||||
| chr4:15040362 | A | G | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2177-102A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 5/11 | chr4 | 15040362 | |||||||
| chr4:15040518 | T | G | 30 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(27): Show |
40 | HG00408.hp2 HG00621.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.2200+31T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040518 | |||||||
| chr4:15040621 | C | T | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2200+134C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040621 | |||||||
| chr4:15040648 | C | A | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2200+161C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040648 | |||||||
| chr4:15040862 | A | G | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2200+375A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040862 | |||||||
| chr4:15040942 | C | G | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2200+455C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040942 | |||||||
| chr4:15040944 | G | A | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2200+457G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15040944 | |||||||
| chr4:15041405 | CT | C | 52 | a0001c0001t0002g0147 a0001c0001t0004g0166 a0002c0002t0002g0005 others(49): Show |
73 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2200+932delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15041405 | ||||||
| chr4:15041411 | T | C | 2 | a0001c0001t0003g0032 a0001c0001t0019g0032 |
2 | HG01346.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2200+924T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041411 | |||||||
| chr4:15041526 | C | T | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2200+1039C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041526 | |||||||
| chr4:15041527 | C | G | 1 | a0018c0024t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2200+1040C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041527 | |||||||
| chr4:15041551 | T | C | 89 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
116 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.2200+1064T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041551 | |||||||
| chr4:15041552 | G | A | 51 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(48): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.2200+1065G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041552 | |||||||
| chr4:15041613 | G | A | 2 | a0013c0018t0001g0106 a0013c0018t0001g0107 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2200+1126G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041613 | |||||||
| chr4:15041648 | C | T | 1 | a0014c0019t0001g0109 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2200+1161C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041648 | |||||||
| chr4:15041654 | C | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2200+1167C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041654 | |||||||
| chr4:15041688 | C | T | 1 | a0001c0001t0004g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2200+1201C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041688 | |||||||
| chr4:15041774 | A | G | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2200+1287A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041774 | |||||||
| chr4:15041894 | A | G | 1 | a0001c0001t0004g0172 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2200+1407A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15041894 | |||||||
| chr4:15042003 | G | C | 2 | a0001c0001t0003g0032 a0001c0001t0019g0032 |
2 | HG01346.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2200+1516G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042003 | |||||||
| chr4:15042115 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(173): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2200+1628G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042115 | |||||||
| chr4:15042172 | A | C | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2200+1685A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042172 | |||||||
| chr4:15042371 | G | A | 1 | a0001c0001t0004g0168 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2200+1884G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042371 | |||||||
| chr4:15042452 | T | C | 1 | a0002c0002t0002g0086 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2200+1965T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042452 | |||||||
| chr4:15042542 | A | T | 17 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(14): Show |
21 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2200+2055A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042542 | |||||||
| chr4:15042642 | G | A | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2200+2155G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042642 | |||||||
| chr4:15042714 | G | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0144 a0001c0001t0003g0145 others(1): Show |
5 | HG01123.hp1 HG01169.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200+2227G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042714 | |||||||
| chr4:15042827 | T | C | 6 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(3): Show |
9 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2200+2340T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042827 | |||||||
| chr4:15042903 | A | G | 1 | a0005c0005t0005g0039 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2200+2416A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15042903 | |||||||
| chr4:15043030 | A | G | 4 | a0005c0005t0005g0037 a0005c0005t0005g0038 a0005c0005t0005g0040 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2200+2543A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15043030 | |||||||
| chr4:15043492 | A | G | 1 | a0003c0003t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2200+3005A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15043492 | |||||||
| chr4:15043892 | A | G | 1 | a0001c0001t0003g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2200+3405A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15043892 | |||||||
| chr4:15043916 | C | T | 1 | a0012c0014t0004g0171 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2200+3429C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15043916 | |||||||
| chr4:15043963 | G | A | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2200+3476G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15043963 | |||||||
| chr4:15044004 | A | G | 1 | a0002c0017t0002g0019 | 2 | NA18979.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2200+3517A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044004 | |||||||
| chr4:15044272 | A | G | 99 | a0001c0001t0001g0004 a0001c0001t0002g0147 a0001c0001t0003g0004 others(96): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.2200+3785A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044272 | |||||||
| chr4:15044585 | A | G | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2200+4098A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044585 | |||||||
| chr4:15044731 | T | C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2200+4244T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044731 | |||||||
| chr4:15044761 | T | C | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2200+4274T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044761 | |||||||
| chr4:15044765 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2200+4278G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044765 | |||||||
| chr4:15044845 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2200+4358G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044845 | |||||||
| chr4:15044984 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2200+4497G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15044984 | |||||||
| chr4:15045114 | C | A | 1 | a0002c0002t0002g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2200+4627C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045114 | |||||||
| chr4:15045209 | C | A | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2200+4722C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045209 | |||||||
| chr4:15045267 | T | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2200+4780T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045267 | |||||||
| chr4:15045299 | A | G | 1 | a0010c0010t0007g0101 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2200+4812A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045299 | |||||||
| chr4:15045654 | G | A | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2200+5167G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045654 | |||||||
| chr4:15045825 | AT | A | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200+5339delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045825 | |||||||
| chr4:15045904 | G | A | 1 | a0001c0001t0004g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2200+5417G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045904 | |||||||
| chr4:15045957 | T | C | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2200+5470T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045957 | |||||||
| chr4:15045960 | G | A | 1 | a0005c0005t0005g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2200+5473G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15045960 | |||||||
| chr4:15046023 | T | C | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2200+5536T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046023 | |||||||
| chr4:15046109 | TG | T | 3 | a0001c0001t0003g0175 a0001c0001t0003g0191 a0015c0029t0003g0194 |
3 | HG00735.hp2 HG00741.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2200+5624delG | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15046109 | ||||||
| chr4:15046329 | G | A | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2200+5842G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046329 | |||||||
| chr4:15046338 | G | T | 1 | a0001c0001t0004g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2200+5851G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046338 | |||||||
| chr4:15046414 | C | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2200+5927C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046414 | |||||||
| chr4:15046441 | G | A | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2200+5954G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046441 | |||||||
| chr4:15046673 | C | A | 1 | a0003c0003t0001g0136 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2201-5741C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046673 | |||||||
| chr4:15046771 | G | C | 1 | a0003c0003t0001g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2201-5643G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046771 | |||||||
| chr4:15046914 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2201-5500C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15046914 | |||||||
| chr4:15047038 | A | G | 1 | a0001c0001t0003g0205 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2201-5376A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047038 | |||||||
| chr4:15047049 | T | C | 1 | a0001c0001t0003g0150 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2201-5365T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047049 | |||||||
| chr4:15047094 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2201-5320G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047094 | |||||||
| chr4:15047096 | A | G | 2 | a0004c0004t0006g0050 a0004c0004t0006g0051 |
2 | HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2201-5318A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047096 | |||||||
| chr4:15047133 | C | G | 28 | a0001c0001t0003g0178 a0001c0001t0004g0001 a0001c0001t0004g0003 others(25): Show |
47 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2201-5281C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047133 | |||||||
| chr4:15047158 | C | G | 46 | a0001c0001t0002g0147 a0001c0001t0003g0177 a0002c0002t0002g0005 others(43): Show |
65 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.2201-5256C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047158 | |||||||
| chr4:15047714 | T | C | 1 | a0002c0002t0002g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2201-4700T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047714 | |||||||
| chr4:15047914 | G | GT | 58 | a0001c0001t0002g0147 a0001c0001t0003g0177 a0002c0002t0002g0005 others(55): Show |
80 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2201-4487dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15047914 | ||||||
| chr4:15047914 | GT | G | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2201-4487delT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15047914 | ||||||
| chr4:15047959 | G | A | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2201-4455G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047959 | |||||||
| chr4:15047965 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0014c0019t0001g0109 |
4 | HG02559.hp1 HG02622.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2201-4449C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047965 | |||||||
| chr4:15047992 | T | C | 4 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2201-4422T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15047992 | |||||||
| chr4:15048032 | A | G | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2201-4382A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048032 | |||||||
| chr4:15048063 | G | C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2201-4351G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048063 | |||||||
| chr4:15048152 | T | G | 1 | a0005c0005t0005g0044 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2201-4262T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048152 | |||||||
| chr4:15048168 | A | G | 1 | a0001c0001t0003g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2201-4246A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048168 | |||||||
| chr4:15048387 | T | C | 1 | a0001c0001t0004g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2201-4027T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048387 | |||||||
| chr4:15048394 | T | G | 25 | a0001c0001t0003g0008 a0001c0001t0003g0030 a0001c0001t0003g0032 others(22): Show |
28 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2201-4020T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048394 | |||||||
| chr4:15048807 | C | T | 1 | a0001c0001t0023g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2201-3607C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15048807 | |||||||
| chr4:15049028 | T | C | 1 | a0002c0002t0002g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2201-3386T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049028 | |||||||
| chr4:15049094 | C | T | 15 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(12): Show |
17 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2201-3320C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049094 | |||||||
| chr4:15049102 | T | G | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2201-3312T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049102 | |||||||
| chr4:15049401 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2201-3013T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049401 | |||||||
| chr4:15049447 | A | AT | 86 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(83): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2201-2960dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15049447 | ||||||
| chr4:15049467 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2201-2947T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049467 | |||||||
| chr4:15049822 | C | T | 12 | a0001c0001t0003g0178 a0001c0001t0004g0001 a0001c0001t0004g0007 others(9): Show |
25 | HG00609.hp1 HG00639.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2201-2592C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049822 | |||||||
| chr4:15049853 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2201-2561T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049853 | |||||||
| chr4:15049978 | T | G | 56 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2201-2436T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15049978 | |||||||
| chr4:15050000 | T | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2201-2414T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050000 | |||||||
| chr4:15050046 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(43): Show |
61 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2201-2368G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050046 | |||||||
| chr4:15050110 | C | A | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
61 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2201-2304C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050110 | |||||||
| chr4:15050154 | A | C | 1 | a0001c0001t0004g0170 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2201-2260A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050154 | |||||||
| chr4:15050367 | A | G | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2201-2047A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050367 | |||||||
| chr4:15050401 | G | A | 4 | a0005c0005t0005g0037 a0005c0005t0005g0038 a0005c0005t0005g0040 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2201-2013G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050401 | |||||||
| chr4:15050556 | A | G | 1 | a0003c0003t0001g0135 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2201-1858A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050556 | |||||||
| chr4:15050775 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG02486.hp2 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2201-1639G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050775 | |||||||
| chr4:15050852 | A | C | 1 | a0005c0005t0005g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2201-1562A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050852 | |||||||
| chr4:15050889 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0159 others(1): Show |
5 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2201-1525T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050889 | |||||||
| chr4:15050984 | C | T | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2201-1430C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15050984 | |||||||
| chr4:15051061 | T | C | 1 | a0005c0005t0005g0040 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2201-1353T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051061 | |||||||
| chr4:15051298 | T | C | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2201-1116T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051298 | |||||||
| chr4:15051323 | T | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(83): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2201-1091T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051323 | |||||||
| chr4:15051529 | CCTCACTA others(15): Show |
C | 3 | a0004c0004t0006g0017 a0004c0004t0006g0045 a0004c0004t0024g0056 |
4 | HG00423.hp2 HG02165.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.2201-881_2201-860d others(24): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 15051529 | ||||||
| chr4:15051856 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2201-558C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051856 | |||||||
| chr4:15051857 | G | A | 1 | a0006c0012t0016g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2201-557G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051857 | |||||||
| chr4:15051857 | G | T | 1 | a0002c0002t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2201-557G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051857 | |||||||
| chr4:15051964 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2201-450G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15051964 | |||||||
| chr4:15052058 | T | G | 7 | a0010c0010t0007g0011 a0010c0010t0007g0101 a0010c0010t0007g0102 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2201-356T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15052058 | |||||||
| chr4:15052120 | T | C | 1 | a0007c0013t0009g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2201-294T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15052120 | |||||||
| chr4:15052134 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0014c0019t0001g0109 |
4 | HG02559.hp1 HG02622.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2201-280A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15052134 | |||||||
| chr4:15052298 | T | G | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2201-116T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15052298 | |||||||
| chr4:15052315 | T | G | 1 | a0001c0001t0023g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2201-99T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 6/11 | chr4 | 15052315 | |||||||
| chr4:15052746 | A | G | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2371+162A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15052746 | |||||||
| chr4:15052922 | T | C | 8 | a0006c0007t0013g0099 a0010c0010t0007g0011 a0010c0010t0007g0101 others(5): Show |
9 | HG01884.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2371+338T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15052922 | |||||||
| chr4:15053023 | A | T | 30 | a0001c0001t0003g0014 a0001c0001t0003g0178 a0001c0001t0003g0179 others(27): Show |
49 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.2371+439A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053023 | |||||||
| chr4:15053026 | T | TA | 54 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(51): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.2371+442_2371+443i others(3): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053026 | |||||||
| chr4:15053027 | T | A | 1 | a0007c0013t0009g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2371+443T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053027 | |||||||
| chr4:15053166 | G | A | 1 | a0002c0002t0002g0082 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2371+582G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053166 | |||||||
| chr4:15053179 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2371+595G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053179 | |||||||
| chr4:15053207 | G | A | 1 | a0002c0002t0014g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2371+623G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053207 | |||||||
| chr4:15053315 | C | T | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2371+731C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053315 | |||||||
| chr4:15053498 | G | A | 1 | a0003c0003t0001g0027 | 2 | HG00099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2372-630G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15053498 | |||||||
| chr4:15054049 | C | T | 36 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0154 others(33): Show |
56 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2372-79C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15054049 | |||||||
| chr4:15054080 | C | T | 3 | a0009c0009t0001g0012 a0009c0009t0001g0126 a0009c0009t0011g0012 |
4 | HG00735.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2372-48C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 7/11 | chr4 | 15054080 | |||||||
| chr4:15054460 | T | C | 1 | a0001c0001t0004g0172 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2461+243T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15054460 | |||||||
| chr4:15054574 | T | A | 1 | a0007c0013t0009g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2461+357T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15054574 | |||||||
| chr4:15054742 | A | G | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2461+525A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15054742 | |||||||
| chr4:15054746 | G | A | 1 | a0007c0016t0001g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2461+529G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15054746 | |||||||
| chr4:15054781 | A | T | 1 | a0003c0003t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2461+564A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15054781 | |||||||
| chr4:15055151 | T | C | 4 | a0003c0003t0001g0027 a0003c0003t0001g0122 a0003c0003t0001g0141 others(1): Show |
5 | HG00099.hp2 HG00639.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2461+934T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055151 | |||||||
| chr4:15055165 | A | G | 2 | a0007c0016t0001g0047 a0007c0016t0001g0048 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2461+948A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055165 | |||||||
| chr4:15055205 | G | GT | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2461+995dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 15055205 | ||||||
| chr4:15055453 | A | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2461+1236A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055453 | |||||||
| chr4:15055461 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2461+1244C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055461 | |||||||
| chr4:15055564 | T | G | 1 | a0008c0008t0001g0112 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2461+1347T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055564 | |||||||
| chr4:15055637 | C | T | 1 | a0001c0001t0004g0190 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2461+1420C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055637 | |||||||
| chr4:15055660 | T | G | 57 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(54): Show |
77 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.2461+1443T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055660 | |||||||
| chr4:15055706 | A | C | 1 | a0006c0007t0013g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2461+1489A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055706 | |||||||
| chr4:15055738 | C | T | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2461+1521C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055738 | |||||||
| chr4:15055841 | A | G | 1 | a0007c0016t0001g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2461+1624A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055841 | |||||||
| chr4:15055948 | G | A | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2461+1731G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15055948 | |||||||
| chr4:15056002 | C | G | 1 | a0003c0003t0001g0136 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2461+1785C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056002 | |||||||
| chr4:15056038 | T | G | 1 | a0002c0002t0002g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2461+1821T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056038 | |||||||
| chr4:15056077 | C | T | 4 | a0002c0002t0002g0080 a0002c0002t0002g0081 a0002c0002t0002g0082 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2461+1860C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056077 | |||||||
| chr4:15056140 | G | A | 1 | a0002c0002t0002g0072 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2461+1923G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056140 | |||||||
| chr4:15056243 | T | C | 56 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2461+2026T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056243 | |||||||
| chr4:15056328 | A | G | 218 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(215): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2462-2093A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056328 | |||||||
| chr4:15056350 | T | C | 2 | a0001c0001t0003g0201 a0001c0001t0003g0205 |
2 | HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2462-2071T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056350 | |||||||
| chr4:15056436 | A | C | 53 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(50): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2462-1985A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056436 | |||||||
| chr4:15056509 | C | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2462-1912C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056509 | |||||||
| chr4:15056621 | A | G | 139 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0108 others(136): Show |
180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.2462-1800A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056621 | |||||||
| chr4:15056678 | C | T | 2 | a0013c0018t0001g0106 a0013c0018t0001g0107 |
2 | HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2462-1743C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056678 | |||||||
| chr4:15056990 | C | T | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2462-1431C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15056990 | |||||||
| chr4:15057212 | T | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0159 others(3): Show |
7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2462-1209T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057212 | |||||||
| chr4:15057481 | T | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0108 others(134): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2462-940T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057481 | |||||||
| chr4:15057482 | G | A | 55 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(52): Show |
75 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.2462-939G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057482 | |||||||
| chr4:15057595 | T | C | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2462-826T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057595 | |||||||
| chr4:15057643 | T | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2462-778T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057643 | |||||||
| chr4:15057780 | C | T | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2462-641C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057780 | |||||||
| chr4:15057813 | C | A | 43 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(40): Show |
56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.2462-608C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057813 | |||||||
| chr4:15057823 | G | A | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2462-598G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057823 | |||||||
| chr4:15057924 | G | T | 1 | a0007c0013t0009g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2462-497G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15057924 | |||||||
| chr4:15058078 | A | G | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2462-343A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15058078 | |||||||
| chr4:15058325 | T | G | 6 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0039 others(3): Show |
9 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2462-96T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15058325 | |||||||
| chr4:15058363 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2462-58A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15058363 | |||||||
| chr4:15058364 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2462-57A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 8/11 | chr4 | 15058364 | |||||||
| chr4:15058571 | A | C | 7 | a0010c0010t0007g0011 a0010c0010t0007g0101 a0010c0010t0007g0102 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2580+32A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058571 | |||||||
| chr4:15058626 | A | G | 7 | a0010c0010t0007g0011 a0010c0010t0007g0101 a0010c0010t0007g0102 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2580+87A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058626 | |||||||
| chr4:15058694 | C | A | 1 | a0013c0018t0001g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2580+155C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058694 | |||||||
| chr4:15058859 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2580+320C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058859 | |||||||
| chr4:15058863 | C | T | 4 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(1): Show |
5 | HG02257.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2580+324C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058863 | |||||||
| chr4:15058934 | C | A | 10 | a0005c0005t0005g0009 a0005c0005t0005g0016 a0005c0005t0005g0037 others(7): Show |
13 | HG00323.hp2 HG00423.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2581-253C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058934 | |||||||
| chr4:15058948 | A | C | 2 | a0001c0001t0003g0033 a0001c0001t0003g0181 |
3 | HG00323.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2581-239A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15058948 | |||||||
| chr4:15059017 | C | T | 4 | a0005c0005t0005g0037 a0005c0005t0005g0038 a0005c0005t0005g0040 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2581-170C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15059017 | |||||||
| chr4:15059156 | G | C | 1 | a0002c0002t0002g0022 | 2 | NA18990.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2581-31G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 9/11 | chr4 | 15059156 | |||||||
| chr4:15059369 | G | T | 1 | a0013c0022t0001g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2695+68G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059369 | |||||||
| chr4:15059408 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2695+107C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059408 | |||||||
| chr4:15059503 | G | T | 1 | a0001c0001t0003g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2695+202G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059503 | |||||||
| chr4:15059518 | A | G | 45 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(42): Show |
63 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.2695+217A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059518 | |||||||
| chr4:15059544 | C | A | 1 | a0004c0004t0006g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2695+243C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059544 | |||||||
| chr4:15059573 | C | G | 7 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0201 others(4): Show |
11 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2695+272C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059573 | |||||||
| chr4:15059764 | C | G | 1 | a0001c0001t0003g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2695+463C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059764 | |||||||
| chr4:15059788 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2695+487A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059788 | |||||||
| chr4:15059870 | A | C | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2695+569A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059870 | |||||||
| chr4:15059906 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2695+605G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15059906 | |||||||
| chr4:15060240 | G | A | 1 | a0001c0001t0003g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2695+939G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060240 | |||||||
| chr4:15060290 | G | A | 1 | a0002c0002t0020g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2695+989G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060290 | |||||||
| chr4:15060353 | A | G | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1052A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060353 | |||||||
| chr4:15060619 | G | A | 1 | a0006c0007t0026g0090 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2695+1318G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060619 | |||||||
| chr4:15060636 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2695+1335G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060636 | |||||||
| chr4:15060864 | C | T | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2696-1215C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060864 | |||||||
| chr4:15060919 | A | C | 2 | a0001c0001t0003g0144 a0001c0001t0003g0146 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2696-1160A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060919 | |||||||
| chr4:15060923 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2696-1156T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15060923 | |||||||
| chr4:15061146 | C | G | 4 | a0002c0002t0002g0080 a0002c0002t0002g0081 a0002c0002t0002g0082 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-933C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061146 | |||||||
| chr4:15061510 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2696-569A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061510 | |||||||
| chr4:15061766 | A | T | 44 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(41): Show |
62 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.2696-313A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061766 | |||||||
| chr4:15061771 | A | C | 4 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-308A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061771 | |||||||
| chr4:15061788 | A | G | 2 | a0006c0012t0001g0010 a0006c0012t0001g0096 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-291A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061788 | |||||||
| chr4:15061848 | A | G | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2696-231A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061848 | |||||||
| chr4:15061870 | TAGGTAGA others(4): Show |
T | 1 | a0006c0007t0013g0099 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2696-207_2696-197d others(13): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 15061870 | ||||||
| chr4:15061886 | T | G | 80 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0153 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2696-193T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061886 | |||||||
| chr4:15061921 | C | T | 88 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(85): Show |
113 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.2696-158C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061921 | |||||||
| chr4:15061984 | T | C | 1 | a0001c0001t0003g0176 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2696-95T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 10/11 | chr4 | 15061984 | |||||||
| chr4:15062328 | A | G | 1 | a0017c0027t0001g0133 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2877+68A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15062328 | |||||||
| chr4:15062330 | G | A | 1 | a0018c0024t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2877+70G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15062330 | |||||||
| chr4:15062480 | G | T | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2877+220G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15062480 | |||||||
| chr4:15062509 | C | G | 8 | a0002c0002t0002g0064 a0002c0002t0002g0070 a0002c0002t0002g0073 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2877+249C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15062509 | |||||||
| chr4:15063066 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2877+806G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15063066 | |||||||
| chr4:15063329 | G | GT | 17 | a0006c0007t0008g0024 a0006c0007t0008g0088 a0006c0007t0008g0089 others(14): Show |
21 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2877+1077dupT | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 15063329 | ||||||
| chr4:15063334 | T | TTG | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2877+1075_2877+107 others(6): Show |
CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 15063334 | ||||||
| chr4:15063341 | T | C | 1 | a0002c0002t0002g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2877+1081T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15063341 | |||||||
| chr4:15063352 | C | G | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2877+1092C>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15063352 | |||||||
| chr4:15063368 | CA | C | 90 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(87): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2877+1120delA | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 15063368 | ||||||
| chr4:15063434 | C | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+1174C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15063434 | |||||||
| chr4:15063776 | A | T | 5 | a0007c0013t0009g0091 a0007c0013t0009g0093 a0007c0013t0009g0094 others(2): Show |
5 | HG02818.hp1 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+1516A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15063776 | |||||||
| chr4:15064412 | T | C | 2 | a0006c0012t0016g0098 a0018c0024t0001g0087 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2878-1741T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064412 | |||||||
| chr4:15064438 | T | C | 1 | a0003c0003t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2878-1715T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064438 | |||||||
| chr4:15064567 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(53): Show |
71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.2878-1586A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064567 | |||||||
| chr4:15064579 | T | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0031 others(174): Show |
239 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.2878-1574T>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064579 | |||||||
| chr4:15064834 | A | C | 12 | a0004c0004t0006g0017 a0004c0004t0006g0018 a0004c0004t0006g0045 others(9): Show |
14 | HG00423.hp2 HG00609.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2878-1319A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064834 | |||||||
| chr4:15064927 | A | C | 3 | a0008c0008t0001g0028 a0008c0008t0001g0111 a0008c0008t0001g0132 |
4 | HG00140.hp2 HG00741.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2878-1226A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15064927 | |||||||
| chr4:15065011 | G | A | 1 | a0003c0003t0001g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2878-1142G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065011 | |||||||
| chr4:15065039 | C | T | 1 | a0003c0003t0001g0120 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2878-1114C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065039 | |||||||
| chr4:15065151 | G | T | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2878-1002G>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065151 | |||||||
| chr4:15065332 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2878-821C>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065332 | |||||||
| chr4:15065402 | T | G | 1 | a0001c0001t0003g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2878-751T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065402 | |||||||
| chr4:15065469 | A | C | 58 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0002g0147 others(55): Show |
80 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2878-684A>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065469 | |||||||
| chr4:15065727 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2878-426C>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065727 | |||||||
| chr4:15065848 | A | T | 2 | a0006c0007t0008g0024 a0006c0007t0008g0089 |
3 | HG02257.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2878-305A>T | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065848 | |||||||
| chr4:15065928 | A | G | 1 | a0001c0001t0003g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2878-225A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065928 | |||||||
| chr4:15065935 | TC | T | 42 | a0001c0001t0002g0147 a0002c0002t0002g0005 a0002c0002t0002g0006 others(39): Show |
60 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.2878-217delC | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065935 | |||||||
| chr4:15065946 | G | A | 3 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 |
3 | HG02451.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2878-207G>A | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065946 | |||||||
| chr4:15065956 | T | G | 55 | a0001c0001t0001g0004 a0001c0001t0003g0004 a0001c0001t0003g0008 others(52): Show |
70 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.2878-197T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065956 | |||||||
| chr4:15065977 | A | G | 4 | a0007c0016t0001g0046 a0007c0016t0001g0047 a0007c0016t0001g0048 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878-176A>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065977 | |||||||
| chr4:15065995 | T | G | 1 | a0018c0024t0001g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2878-158T>G | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15065995 | |||||||
| chr4:15066064 | T | C | 4 | a0007c0013t0009g0093 a0007c0013t0009g0094 a0007c0013t0009g0095 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2878-89T>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15066064 | |||||||
| chr4:15066073 | G | C | 1 | a0002c0002t0002g0066 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2878-80G>C | CPEB2 | ENSG00000137449.17 | transcript | ENST00000538197.7 | protein_coding | 11/11 | chr4 | 15066073 |