Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10658 |
| ensemblid | ENSG00000149187.19 |
| hgncid | 2549 |
| symbol | CELF1 |
| name | CUGBP Elav-like family member 1 |
| refseq_nuc | NM_001376376.1 |
| refseq_prot | NP_001363305.1 |
| ensembl_nuc | ENST00000687097.1 |
| ensembl_prot | ENSP00000508525.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 47465937 |
| end | 47553132 |
| strand | - |
| ver | v1.2 |
| region | chr11:47465937-47553132 |
| region5000 | chr11:47460937-47558132 |
| regionname0 | CELF1_chr11_47465937_47553132 |
| regionname5000 | CELF1_chr11_47460937_47558132 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1542 | 335 | 81 | 55 | 148 | 10 | 39 | CELF1_chr11_47460937_47558132 | CELF1 | ATGGC others(1537): Show |
chr11 | 47460937 | 47558132 | ||
| a0001c0002 | 0/0 | 1542 | 2 | 1 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | ATGGC others(1537): Show |
chr11 | 47460937 | 47558132 | ||
| a0001c0003 | 0/0 | 1542 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | ATGGC others(1537): Show |
chr11 | 47460937 | 47558132 | ||
| a0001c0004 | 0/0 | 1542 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | ATGGC others(1537): Show |
chr11 | 47460937 | 47558132 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8131 | 111 | 37 | 12 | 53 | 2 | 6 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0002 | 0/0 | 8131 | 105 | 12 | 24 | 47 | 5 | 17 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0003 | 0/0 | 8132 | 71 | 3 | 13 | 42 | 2 | 11 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0004 | 0/0 | 8143 | 10 | 10 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8138): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0005 | 0/0 | 8132 | 6 | 6 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0006 | 0/0 | 8131 | 5 | 0 | 3 | 0 | 1 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0007 | 0/0 | 8133 | 3 | 3 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8128): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0008 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0009 | 0/0 | 8132 | 2 | 0 | 0 | 2 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0010 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0012 | 0/0 | 8131 | 2 | 0 | 0 | 0 | 0 | 2 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0013 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0014 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0015 | 0/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0016 | 1/0 | 8132 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0017 | 0/0 | 8132 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0018 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0019 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0020 | 0/0 | 8132 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0021 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0022 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0023 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0024 | 0/0 | 8131 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0025 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0026 | 0/0 | 8131 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0027 | 0/0 | 8131 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0001t0028 | 0/0 | 8132 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8127): Show |
chr11 | 47460937 | 47558132 |
| a0001c0002t0002 | 0/0 | 8131 | 2 | 1 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0003t0011 | 0/0 | 8131 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| a0001c0004t0002 | 0/0 | 8131 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | GTGTT others(8126): Show |
chr11 | 47460937 | 47558132 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0012g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0013g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0016g0337 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0017g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0022g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0023g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0024g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0025g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0026g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0027g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0001t0028g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0003t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0003t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| a0001c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0315 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0077 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0111 | EUR | FIN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00558 | hp1 | a0001 | c0001 | t0009 | g0132 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00735 | hp2 | a0001 | c0001 | t0028 | g0034 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0104 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0300 | AMR | PUR | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0079 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0117 | AMR | CLM | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0050 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0310 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0316 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0275 | EUR | IBS | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0299 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02165 | hp2 | a0001 | c0001 | t0026 | g0291 | EAS | CDX | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0255 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02293 | hp2 | a0001 | c0001 | t0021 | g0082 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0138 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02683 | hp1 | a0001 | c0001 | t0027 | g0225 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02896 | hp1 | a0001 | c0003 | t0011 | g0308 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0101 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0102 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0211 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02976 | hp2 | a0001 | c0001 | t0024 | g0320 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03098 | hp2 | a0001 | c0003 | t0011 | g0309 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0333 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03491 | hp1 | a0001 | c0001 | t0012 | g0251 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0258 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0221 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0038 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0114 | SAS | PJL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0064 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04184 | hp2 | a0001 | c0004 | t0002 | g0303 | SAS | BEB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19060 | hp2 | a0001 | c0001 | t0022 | g0149 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19089 | hp2 | a0001 | c0001 | t0025 | g0284 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19090 | hp1 | a0001 | c0001 | t0020 | g0097 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ASW | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ASW | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | TSI | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | GIH | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | GIH | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0182 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0332 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ACB | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | USA | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | USA | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | LWK | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0207 | REF | REF | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0016 | g0337 | REF | REF | CELF1_chr11_47460937_47558132 | CELF1 | chr11 | 47460937 | 47558132 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47473134 | A | C | 1 | a0001c0002 | 2 | HG01243.hp2 HG01884.hp2 |
synonymous_variant | LOW | c.1371T>G | p.Ser457Ser | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/15 | 1665/8132 | 1371/1545 | 457/514 | chr11 | 47473134 | |||
| chr11:47473218 | G | A | 1 | a0001c0004 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1287C>T | p.Ala429Ala | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/15 | 1581/8132 | 1287/1545 | 429/514 | chr11 | 47473218 | |||
| chr11:47478887 | G | A | 1 | a0001c0003 | 2 | HG02896.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.834C>T | p.His278His | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/15 | 1128/8132 | 834/1545 | 278/514 | chr11 | 47478887 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47466046 | C | A | 1 | a0001c0001t0021 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6184G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6184 | chr11 | 47466046 | ||||||
| chr11:47466124 | A | G | 1 | a0001c0001t0020 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6106T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6106 | chr11 | 47466124 | ||||||
| chr11:47466130 | A | AT | 1 | a0001c0001t0005 | 6 | HG02258.hp2 HG02486.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6099dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6099 | chr11 | 47466130 | ||||||
| chr11:47466188 | G | A | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
208 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*6042C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 6042 | chr11 | 47466188 | ||||||
| chr11:47466231 | A | T | 1 | a0001c0001t0022 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5999T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5999 | chr11 | 47466231 | ||||||
| chr11:47466562 | C | CT | 7 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0014 others(4): Show |
78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5667dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5667 | chr11 | 47466562 | ||||||
| chr11:47466783 | A | G | 1 | a0001c0001t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5447T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5447 | chr11 | 47466783 | ||||||
| chr11:47467038 | G | A | 1 | a0001c0001t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5192C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 5192 | chr11 | 47467038 | ||||||
| chr11:47467319 | A | C | 1 | a0001c0001t0004 | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4911T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4911 | chr11 | 47467319 | ||||||
| chr11:47467522 | T | C | 1 | a0001c0001t0024 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4708A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4708 | chr11 | 47467522 | ||||||
| chr11:47467595 | G | A | 1 | a0001c0001t0025 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4635C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4635 | chr11 | 47467595 | ||||||
| chr11:47467700 | C | T | 1 | a0001c0001t0008 | 2 | HG02258.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4530G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4530 | chr11 | 47467700 | ||||||
| chr11:47468148 | G | C | 1 | a0001c0001t0006 | 5 | HG00323.hp2 HG01081.hp1 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4082C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4082 | chr11 | 47468148 | ||||||
| chr11:47468227 | A | AAG | 1 | a0001c0001t0007 | 3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4001_*4002dupCT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 4002 | chr11 | 47468227 | ||||||
| chr11:47468398 | G | A | 1 | a0001c0001t0015 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3832C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 3832 | chr11 | 47468398 | ||||||
| chr11:47468732 | G | C | 1 | a0001c0001t0026 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 3498 | chr11 | 47468732 | ||||||
| chr11:47469392 | T | C | 1 | a0001c0001t0027 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2838A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2838 | chr11 | 47469392 | ||||||
| chr11:47469653 | G | A | 1 | a0001c0001t0010 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2577C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2577 | chr11 | 47469653 | ||||||
| chr11:47469723 | G | A | 1 | a0001c0003t0011 | 2 | HG02896.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2507C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2507 | chr11 | 47469723 | ||||||
| chr11:47469856 | A | G | 1 | a0001c0001t0018 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2374T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2374 | chr11 | 47469856 | ||||||
| chr11:47470224 | G | A | 1 | a0001c0001t0028 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2006C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 2006 | chr11 | 47470224 | ||||||
| chr11:47470286 | CT | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
3_prime_UTR_variant | MODIFIER | c.*1943delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1943 | chr11 | 47470286 | ||||||
| chr11:47470497 | A | G | 1 | a0001c0001t0015 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1733 | chr11 | 47470497 | ||||||
| chr11:47470621 | C | T | 1 | a0001c0001t0014 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1609G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 1609 | chr11 | 47470621 | ||||||
| chr11:47471881 | C | T | 1 | a0001c0001t0013 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*349G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 349 | chr11 | 47471881 | ||||||
| chr11:47471897 | T | C | 1 | a0001c0001t0012 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*333A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 15/15 | 333 | chr11 | 47471897 | ||||||
| chr11:47553014 | C | CGCTGCCT others(5): Show |
1 | a0001c0001t0004 | 10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-188_-177dupAACTGA others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/15 | 53492 | chr11 | 47553014 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:47472432 | A | G | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1418-75T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472432 | |||||||
| chr11:47472701 | C | T | 1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1418-344G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472701 | |||||||
| chr11:47472843 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+245T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472843 | |||||||
| chr11:47472989 | A | C | 4 | a0001c0001t0001g0026 a0001c0001t0002g0108 a0001c0002t0002g0299 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1417+99T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 14/14 | chr11 | 47472989 | |||||||
| chr11:47473278 | C | T | 6 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(3): Show |
6 | HG03942.hp1 NA18952.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-47G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473278 | |||||||
| chr11:47473352 | C | A | 1 | a0001c0001t0002g0030 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1274-121G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473352 | |||||||
| chr11:47473367 | G | C | 3 | a0001c0001t0002g0108 a0001c0002t0002g0299 a0001c0002t0002g0300 |
3 | HG01243.hp2 HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1274-136C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473367 | |||||||
| chr11:47473389 | G | A | 1 | a0001c0002t0002g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1274-158C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473389 | |||||||
| chr11:47473650 | G | A | 110 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(107): Show |
110 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1274-419C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473650 | |||||||
| chr11:47473662 | G | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1274-431C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473662 | |||||||
| chr11:47473682 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1274-451C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473682 | |||||||
| chr11:47473897 | TTTTCTTT others(7): Show |
T | 114 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(111): Show |
114 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1274-680_1274-667d others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47473897 | |||||||
| chr11:47474194 | G | T | 87 | a0001c0001t0001g0022 a0001c0001t0002g0076 a0001c0001t0003g0014 others(84): Show |
88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1274-963C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474194 | |||||||
| chr11:47474468 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1273+868T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474468 | |||||||
| chr11:47474636 | T | A | 1 | a0001c0001t0002g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1273+700A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474636 | |||||||
| chr11:47474661 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1273+675T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474661 | |||||||
| chr11:47474754 | C | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0198 others(1): Show |
4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1273+582G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474754 | |||||||
| chr11:47474843 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1273+493G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474843 | |||||||
| chr11:47474971 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+365G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47474971 | |||||||
| chr11:47475093 | C | T | 1 | a0001c0001t0008g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1273+243G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47475093 | |||||||
| chr11:47475275 | C | T | 24 | a0001c0001t0002g0011 a0001c0001t0002g0013 a0001c0001t0002g0105 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1273+61G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 13/14 | chr11 | 47475275 | |||||||
| chr11:47475591 | G | A | 1 | a0001c0001t0026g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1088-70C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475591 | |||||||
| chr11:47475606 | G | C | 1 | a0001c0001t0002g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1088-85C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475606 | |||||||
| chr11:47475729 | A | C | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1088-208T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475729 | |||||||
| chr11:47475735 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1088-214C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475735 | |||||||
| chr11:47475742 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1088-221C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475742 | |||||||
| chr11:47475999 | A | AT | 6 | a0001c0001t0001g0191 a0001c0001t0002g0259 a0001c0001t0002g0260 others(3): Show |
6 | HG01169.hp2 HG01175.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-479dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47475999 | |||||||
| chr11:47476220 | T | C | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1087+626A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476220 | |||||||
| chr11:47476383 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1087+463G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476383 | |||||||
| chr11:47476397 | C | G | 6 | a0001c0001t0001g0319 a0001c0001t0010g0101 a0001c0001t0010g0102 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087+449G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476397 | |||||||
| chr11:47476435 | T | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+411A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476435 | |||||||
| chr11:47476526 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1087+320A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476526 | |||||||
| chr11:47476736 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1087+110A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 12/14 | chr11 | 47476736 | |||||||
| chr11:47477108 | T | C | 6 | a0001c0001t0001g0319 a0001c0001t0010g0101 a0001c0001t0010g0102 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-149A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477108 | |||||||
| chr11:47477137 | T | C | 1 | a0001c0001t0002g0029 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.973+160A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477137 | |||||||
| chr11:47477210 | A | C | 1 | a0001c0001t0003g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+87T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477210 | |||||||
| chr11:47477249 | C | A | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.973+48G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477249 | |||||||
| chr11:47477260 | G | C | 1 | a0001c0001t0003g0066 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.973+37C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 11/14 | chr11 | 47477260 | |||||||
| chr11:47477703 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.845-278G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477703 | |||||||
| chr11:47477860 | A | G | 1 | a0001c0001t0027g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.845-435T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477860 | |||||||
| chr11:47477886 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.845-461G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477886 | |||||||
| chr11:47477968 | G | C | 1 | a0001c0001t0003g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.845-543C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47477968 | |||||||
| chr11:47478664 | A | AC | 3 | a0001c0001t0002g0283 a0001c0001t0002g0286 a0001c0001t0002g0289 |
3 | NA18956.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.844+212dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478664 | |||||||
| chr11:47478715 | T | C | 108 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.844+162A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478715 | |||||||
| chr11:47478848 | C | T | 59 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.844+29G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 10/14 | chr11 | 47478848 | |||||||
| chr11:47479086 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.769-134G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479086 | |||||||
| chr11:47479109 | T | C | 4 | a0001c0001t0002g0277 a0001c0001t0002g0290 a0001c0001t0002g0292 others(1): Show |
4 | HG00544.hp2 HG01978.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.769-157A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479109 | |||||||
| chr11:47479186 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0171 |
2 | NA18970.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.769-234G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479186 | |||||||
| chr11:47479269 | C | T | 6 | a0001c0001t0001g0319 a0001c0001t0010g0101 a0001c0001t0010g0102 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-317G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479269 | |||||||
| chr11:47479438 | T | A | 6 | a0001c0001t0001g0319 a0001c0001t0010g0101 a0001c0001t0010g0102 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-486A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479438 | |||||||
| chr11:47479656 | C | G | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.769-704G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479656 | |||||||
| chr11:47479688 | T | C | 1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.769-736A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47479688 | |||||||
| chr11:47480067 | T | G | 103 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(100): Show |
103 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.769-1115A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480067 | |||||||
| chr11:47480089 | C | CT | 10 | a0001c0001t0001g0319 a0001c0001t0002g0260 a0001c0001t0003g0037 others(7): Show |
10 | HG02055.hp2 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.769-1138dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480089 | |||||||
| chr11:47480089 | CT | C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0145 a0001c0001t0002g0306 others(4): Show |
7 | HG01081.hp2 HG01257.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.769-1138delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480089 | |||||||
| chr11:47480090 | T | G | 12 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0325 others(9): Show |
12 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.769-1138A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480090 | |||||||
| chr11:47480336 | C | T | 24 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(21): Show |
24 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.769-1384G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480336 | |||||||
| chr11:47480437 | G | T | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.769-1485C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480437 | |||||||
| chr11:47480515 | C | T | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.769-1563G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480515 | |||||||
| chr11:47480552 | C | A | 1 | a0001c0001t0002g0302 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.769-1600G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480552 | |||||||
| chr11:47480738 | T | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-1786A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47480738 | |||||||
| chr11:47481081 | GTTTTTTT others(16): Show |
G | 2 | a0001c0001t0007g0119 a0001c0001t0007g0211 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.768+1591_768+1613d others(25): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | |||||||
| chr11:47481081 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0007g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.768+1590_768+1613d others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | |||||||
| chr11:47481081 | GTTTTTTT others(21): Show |
G | 1 | a0001c0001t0003g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.768+1586_768+1613d others(30): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481081 | |||||||
| chr11:47481082 | T | G | 5 | a0001c0001t0002g0272 a0001c0001t0002g0274 a0001c0001t0002g0275 others(2): Show |
5 | HG01433.hp2 HG01517.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.768+1613A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481082 | |||||||
| chr11:47481093 | T | C | 22 | a0001c0001t0002g0250 a0001c0001t0002g0272 a0001c0001t0002g0273 others(19): Show |
22 | HG00544.hp2 HG00621.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.768+1602A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481093 | |||||||
| chr11:47481095 | TC | T | 67 | a0001c0001t0002g0076 a0001c0001t0003g0014 a0001c0001t0003g0015 others(64): Show |
67 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.768+1599delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481095 | |||||||
| chr11:47481096 | C | T | 6 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(3): Show |
6 | HG00597.hp1 HG01361.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+1599G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481096 | |||||||
| chr11:47481098 | T | C | 5 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG01361.hp1 HG04115.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1597A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481098 | |||||||
| chr11:47481099 | C | T | 5 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG01361.hp1 HG04115.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1596G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481099 | |||||||
| chr11:47481101 | TC | T | 42 | a0001c0001t0002g0076 a0001c0001t0003g0014 a0001c0001t0003g0015 others(39): Show |
42 | HG00323.hp1 HG00597.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.768+1593delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481101 | |||||||
| chr11:47481102 | C | CT | 32 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0001c0001t0001g0140 others(29): Show |
33 | HG00544.hp1 HG01884.hp1 HG02083.hp1 others(30): Show |
intron_variant | MODIFIER | c.768+1592dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | C | CTT | 11 | a0001c0001t0001g0026 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
11 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.768+1591_768+1592d others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | C | CTTT | 82 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(79): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.768+1590_768+1592d others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | C | CTTTT | 18 | a0001c0001t0002g0116 a0001c0001t0002g0223 a0001c0001t0002g0230 others(15): Show |
18 | HG00621.hp2 HG01192.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.768+1589_768+1592d others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | C | T | 35 | a0001c0001t0002g0227 a0001c0001t0002g0234 a0001c0001t0002g0235 others(32): Show |
35 | HG00438.hp2 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.768+1593G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | CT | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0121 others(20): Show |
23 | HG01243.hp1 HG01261.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.768+1592delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481102 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0008g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.768+1575_768+1592d others(20): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481102 | |||||||
| chr11:47481106 | T | C | 1 | a0001c0001t0003g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.768+1589A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481106 | |||||||
| chr11:47481109 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.768+1586A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481109 | |||||||
| chr11:47481198 | G | A | 4 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 others(1): Show |
4 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+1497C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481198 | |||||||
| chr11:47481376 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.768+1319G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481376 | |||||||
| chr11:47481740 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+955G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47481740 | |||||||
| chr11:47482030 | C | T | 9 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0163 others(6): Show |
9 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+665G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482030 | |||||||
| chr11:47482183 | AGAGT | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.768+508_768+511del others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482183 | |||||||
| chr11:47482207 | A | AAAAT | 105 | a0001c0001t0001g0319 a0001c0001t0002g0011 a0001c0001t0002g0012 others(102): Show |
105 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.768+484_768+487dup others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482207 | |||||||
| chr11:47482207 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0002g0232 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.768+480_768+487dup others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482207 | |||||||
| chr11:47482273 | G | T | 1 | a0001c0001t0003g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.768+422C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482273 | |||||||
| chr11:47482523 | G | T | 109 | a0001c0001t0001g0161 a0001c0001t0002g0011 a0001c0001t0002g0012 others(106): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.768+172C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 9/14 | chr11 | 47482523 | |||||||
| chr11:47482890 | C | T | 6 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(3): Show |
6 | HG03942.hp1 NA18952.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-34G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47482890 | |||||||
| chr11:47483097 | TA | T | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.607-242delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483097 | |||||||
| chr11:47483125 | G | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.607-269C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483125 | |||||||
| chr11:47483202 | C | A | 1 | a0001c0001t0002g0235 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.606+251G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483202 | |||||||
| chr11:47483383 | G | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+70C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483383 | |||||||
| chr11:47483400 | G | A | 1 | a0001c0001t0005g0332 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.606+53C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 8/14 | chr11 | 47483400 | |||||||
| chr11:47483567 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0171 |
2 | NA18970.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.527-35A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483567 | |||||||
| chr11:47483761 | C | T | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.527-229G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483761 | |||||||
| chr11:47483981 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.526+408A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47483981 | |||||||
| chr11:47484258 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.526+131A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484258 | |||||||
| chr11:47484317 | C | CA | 14 | a0001c0001t0001g0098 a0001c0001t0001g0147 a0001c0001t0001g0148 others(11): Show |
14 | HG01175.hp1 HG02738.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.526+71dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484317 | |||||||
| chr11:47484331 | C | A | 1 | a0001c0001t0002g0305 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.526+58G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 7/14 | chr11 | 47484331 | |||||||
| chr11:47484588 | G | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.392-65C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484588 | |||||||
| chr11:47484734 | A | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.392-211T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484734 | |||||||
| chr11:47484747 | C | T | 2 | a0001c0001t0002g0290 a0001c0001t0025g0284 |
2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.392-224G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484747 | |||||||
| chr11:47484906 | G | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0098 a0001c0001t0001g0193 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.392-383C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484906 | |||||||
| chr11:47484924 | CGCCTCG | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-407_392-402del others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47484924 | |||||||
| chr11:47485186 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.392-663A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485186 | |||||||
| chr11:47485306 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.392-783C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485306 | |||||||
| chr11:47485500 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.392-977G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485500 | |||||||
| chr11:47485585 | AT | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0198 a0001c0001t0001g0330 others(3): Show |
6 | HG01257.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-1063delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485585 | |||||||
| chr11:47485717 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.391+1033C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485717 | |||||||
| chr11:47485744 | G | A | 1 | a0001c0001t0027g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.391+1006C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47485744 | |||||||
| chr11:47486085 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.391+665G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486085 | |||||||
| chr11:47486090 | G | A | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.391+660C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486090 | |||||||
| chr11:47486160 | CA | C | 231 | a0001c0001t0001g0026 a0001c0001t0001g0159 a0001c0001t0001g0167 others(228): Show |
232 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.391+589delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486160 | |||||||
| chr11:47486294 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.391+456G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486294 | |||||||
| chr11:47486339 | C | A | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.391+411G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486339 | |||||||
| chr11:47486352 | G | A | 1 | a0001c0001t0003g0321 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.391+398C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486352 | |||||||
| chr11:47486495 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.391+255G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 6/14 | chr11 | 47486495 | |||||||
| chr11:47486821 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.343-23A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486821 | |||||||
| chr11:47486910 | T | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-112A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486910 | |||||||
| chr11:47486922 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
14 | HG01496.hp1 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.343-124C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47486922 | |||||||
| chr11:47487043 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.342+116A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 5/14 | chr11 | 47487043 | |||||||
| chr11:47487312 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.260-71G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487312 | |||||||
| chr11:47487465 | A | G | 21 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 others(18): Show |
21 | HG00544.hp2 HG00621.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.260-224T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487465 | |||||||
| chr11:47487585 | G | C | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.260-344C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487585 | |||||||
| chr11:47487813 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.260-572T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487813 | |||||||
| chr11:47487816 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0159 a0001c0001t0001g0172 others(4): Show |
7 | HG00558.hp2 HG00609.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-575C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47487816 | |||||||
| chr11:47488148 | C | A | 18 | a0001c0001t0002g0025 a0001c0001t0002g0222 a0001c0001t0002g0224 others(15): Show |
18 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.259+689G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488148 | |||||||
| chr11:47488161 | T | C | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.259+676A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488161 | |||||||
| chr11:47488175 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.259+662C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488175 | |||||||
| chr11:47488213 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.259+624C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488213 | |||||||
| chr11:47488397 | A | G | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.259+440T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488397 | |||||||
| chr11:47488428 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.259+409G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488428 | |||||||
| chr11:47488529 | G | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.259+308C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488529 | |||||||
| chr11:47488777 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.259+60G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488777 | |||||||
| chr11:47488801 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.259+36C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 4/14 | chr11 | 47488801 | |||||||
| chr11:47489054 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0162 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.72-30A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489054 | |||||||
| chr11:47489195 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0003g0297 a0001c0001t0003g0298 |
3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.72-171G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489195 | |||||||
| chr11:47489536 | AATGC | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-516_72-513delGC others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489536 | |||||||
| chr11:47489863 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.72-839G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489863 | |||||||
| chr11:47489932 | C | CTTGTTT | 3 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0309 |
3 | HG02451.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72-914_72-909dupAA others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489932 | |||||||
| chr11:47489932 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72-909_72-908insAA others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489932 | |||||||
| chr11:47489935 | G | GGTTTTTT others(12): Show |
1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTGTTTTT others(10): Show |
1 | a0001c0001t0002g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTT | 8 | a0001c0001t0001g0144 a0001c0001t0001g0164 a0001c0001t0003g0062 others(5): Show |
8 | HG00639.hp1 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-915_72-912dupAA others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTT | 7 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0001c0001t0003g0070 others(4): Show |
7 | HG02965.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-916_72-912dupAA others(3): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT | 9 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0325 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-918_72-912dupAA others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0122 a0001c0001t0002g0028 a0001c0001t0002g0030 others(5): Show |
8 | HG01071.hp2 HG01099.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-920_72-912dupAA others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0026 a0001c0001t0003g0086 a0001c0001t0004g0002 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.72-921_72-912dupAA others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(4): Show |
6 | a0001c0001t0002g0029 a0001c0001t0003g0040 a0001c0001t0004g0003 others(3): Show |
6 | HG01192.hp2 HG02970.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-922_72-912dupAA others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(5): Show |
3 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0019g0182 |
3 | HG02486.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.72-923_72-912dupAA others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0004g0001 a0001c0001t0004g0009 |
3 | HG01884.hp1 HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.72-924_72-912dupAA others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(7): Show |
7 | a0001c0001t0002g0116 a0001c0001t0002g0264 a0001c0001t0002g0274 others(4): Show |
7 | HG01517.hp2 HG03239.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.72-925_72-912dupAA others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(8): Show |
7 | a0001c0001t0002g0076 a0001c0001t0002g0219 a0001c0001t0002g0273 others(4): Show |
7 | HG01433.hp2 HG01943.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-926_72-912dupAA others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(9): Show |
22 | a0001c0001t0002g0220 a0001c0001t0002g0234 a0001c0001t0002g0235 others(19): Show |
22 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.72-927_72-912dupAA others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(10): Show |
38 | a0001c0001t0001g0098 a0001c0001t0001g0143 a0001c0001t0002g0025 others(35): Show |
38 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.72-928_72-912dupAA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(11): Show |
42 | a0001c0001t0001g0125 a0001c0001t0002g0217 a0001c0001t0002g0222 others(39): Show |
42 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.72-929_72-912dupAA others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(12): Show |
15 | a0001c0001t0001g0120 a0001c0001t0001g0135 a0001c0001t0002g0110 others(12): Show |
15 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.72-930_72-912dupAA others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(13): Show |
13 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0145 others(10): Show |
13 | HG00323.hp1 HG00642.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-931_72-912dupAA others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(14): Show |
9 | a0001c0001t0001g0174 a0001c0001t0002g0247 a0001c0001t0002g0267 others(6): Show |
9 | HG01346.hp2 HG01943.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(19): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(15): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0001g0158 others(4): Show |
7 | HG01261.hp2 HG01358.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(20): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(16): Show |
8 | a0001c0001t0001g0163 a0001c0001t0002g0012 a0001c0001t0002g0226 others(5): Show |
8 | HG00609.hp2 HG01255.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(21): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(17): Show |
3 | a0001c0001t0001g0190 a0001c0001t0002g0316 a0001c0001t0027g0225 |
3 | HG01517.hp1 HG02683.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.72-912_72-911insAA others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0003g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(23): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(19): Show |
4 | a0001c0001t0001g0147 a0001c0001t0002g0311 a0001c0001t0002g0312 others(1): Show |
4 | HG00280.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-912_72-911insAA others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(23): Show |
1 | a0001c0001t0001g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(28): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(24): Show |
1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(29): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(25): Show |
2 | a0001c0001t0001g0162 a0001c0001t0007g0211 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.72-912_72-911insAA others(30): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(26): Show |
1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(31): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(28): Show |
1 | a0001c0001t0006g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(33): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(32): Show |
1 | a0001c0001t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(37): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(33): Show |
1 | a0001c0001t0002g0285 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.72-912_72-911insAA others(38): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | GTTTTTTT others(41): Show |
1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.72-912_72-911insAA others(46): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | G | T | 1 | a0001c0001t0003g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72-911C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489935 | GT | G | 17 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0136 others(14): Show |
17 | HG00558.hp1 HG02071.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.72-912delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489935 | |||||||
| chr11:47489944 | T | TTTTTTTT others(10): Show |
4 | a0001c0001t0002g0237 a0001c0001t0002g0239 a0001c0001t0002g0240 others(1): Show |
4 | HG02083.hp2 NA18944.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-921_72-920insGA others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47489944 | |||||||
| chr11:47490158 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.72-1134G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490158 | |||||||
| chr11:47490183 | G | A | 5 | a0001c0001t0001g0319 a0001c0001t0003g0035 a0001c0001t0024g0320 others(2): Show |
5 | HG01175.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1159C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490183 | |||||||
| chr11:47490425 | G | GT | 20 | a0001c0001t0002g0029 a0001c0001t0002g0237 a0001c0001t0003g0033 others(17): Show |
20 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.72-1402dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490425 | |||||||
| chr11:47490425 | GT | G | 107 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
107 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.72-1402delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490425 | |||||||
| chr11:47490463 | A | C | 2 | a0001c0001t0008g0089 a0001c0001t0008g0099 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.72-1439T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490463 | |||||||
| chr11:47490586 | G | A | 8 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(5): Show |
8 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.72-1562C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490586 | |||||||
| chr11:47490850 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-1826G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490850 | |||||||
| chr11:47490995 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.72-1971C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47490995 | |||||||
| chr11:47491103 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.72-2079G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491103 | |||||||
| chr11:47491250 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.72-2226G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491250 | |||||||
| chr11:47491255 | CA | C | 152 | a0001c0001t0001g0098 a0001c0001t0001g0135 a0001c0001t0002g0011 others(149): Show |
153 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.72-2232delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491255 | |||||||
| chr11:47491256 | AG | A | 55 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(52): Show |
55 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.72-2233delC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491256 | |||||||
| chr11:47491573 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.72-2549T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491573 | |||||||
| chr11:47491578 | A | G | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-2554T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47491578 | |||||||
| chr11:47492218 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0061 |
2 | HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.72-3194C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492218 | |||||||
| chr11:47492354 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-3330G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492354 | |||||||
| chr11:47492586 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.72-3562C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492586 | |||||||
| chr11:47492646 | C | G | 3 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0004 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.72-3622G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492646 | |||||||
| chr11:47492713 | CAG | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-3691_72-3690del others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492713 | |||||||
| chr11:47492849 | A | G | 1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3825T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492849 | |||||||
| chr11:47492862 | A | T | 1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3838T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492862 | |||||||
| chr11:47492863 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72-3839C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47492863 | |||||||
| chr11:47493004 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.72-3980G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493004 | |||||||
| chr11:47493219 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.72-4195T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493219 | |||||||
| chr11:47493238 | GCA | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4216_72-4215del others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493238 | |||||||
| chr11:47493270 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0246 |
2 | HG01167.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.72-4246C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493270 | |||||||
| chr11:47493337 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.72-4313G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493337 | |||||||
| chr11:47493339 | T | TA | 315 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(312): Show |
316 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.72-4316dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493339 | |||||||
| chr11:47493339 | T | TAA | 6 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0175 others(3): Show |
6 | HG02280.hp1 HG03831.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-4317_72-4316dup others(2): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493339 | |||||||
| chr11:47493408 | T | C | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.72-4384A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493408 | |||||||
| chr11:47493432 | C | T | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.72-4408G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493432 | |||||||
| chr11:47493439 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.72-4415G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493439 | |||||||
| chr11:47493483 | G | A | 10 | a0001c0001t0002g0116 a0001c0001t0002g0310 a0001c0001t0002g0311 others(7): Show |
10 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.72-4459C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493483 | |||||||
| chr11:47493507 | CAAAAAGA others(4): Show |
C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4494_72-4484del others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493507 | |||||||
| chr11:47493513 | G | GA | 36 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0001g0140 others(33): Show |
36 | HG00558.hp1 HG00621.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-4490dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493513 | |||||||
| chr11:47493513 | GA | G | 85 | a0001c0001t0001g0098 a0001c0001t0001g0129 a0001c0001t0001g0135 others(82): Show |
86 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.72-4490delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493513 | |||||||
| chr11:47493540 | G | T | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.72-4516C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493540 | |||||||
| chr11:47493597 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.72-4573A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493597 | |||||||
| chr11:47493782 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-4758C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493782 | |||||||
| chr11:47493875 | C | G | 9 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(6): Show |
9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.72-4851G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47493875 | |||||||
| chr11:47494009 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.72-4985A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494009 | |||||||
| chr11:47494189 | G | C | 1 | a0001c0001t0002g0264 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.72-5165C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494189 | |||||||
| chr11:47494204 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.72-5180T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494204 | |||||||
| chr11:47494306 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18985.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.71+5147C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494306 | |||||||
| chr11:47494345 | A | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.71+5108T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494345 | |||||||
| chr11:47494417 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.71+5036C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494417 | |||||||
| chr11:47494502 | A | G | 2 | a0001c0001t0001g0334 a0001c0001t0013g0333 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.71+4951T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494502 | |||||||
| chr11:47494504 | C | T | 3 | a0001c0001t0007g0016 a0001c0001t0007g0119 a0001c0001t0007g0211 |
3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.71+4949G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494504 | |||||||
| chr11:47494786 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0162 |
3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.71+4667G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494786 | |||||||
| chr11:47494888 | T | C | 1 | a0001c0001t0002g0283 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.71+4565A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494888 | |||||||
| chr11:47494909 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.71+4544T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47494909 | |||||||
| chr11:47495053 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.71+4400C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495053 | |||||||
| chr11:47495399 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0177 |
2 | NA18982.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.71+4054A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495399 | |||||||
| chr11:47495452 | G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.71+4001C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495452 | |||||||
| chr11:47495482 | A | C | 2 | a0001c0001t0002g0290 a0001c0001t0025g0284 |
2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.71+3971T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495482 | |||||||
| chr11:47495482 | A | G | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+3971T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495482 | |||||||
| chr11:47495757 | T | A | 1 | a0001c0001t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.71+3696A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47495757 | |||||||
| chr11:47496045 | T | A | 3 | a0001c0001t0002g0076 a0001c0001t0003g0075 a0001c0001t0003g0078 |
3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.71+3408A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496045 | |||||||
| chr11:47496046 | G | C | 1 | a0001c0001t0002g0315 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.71+3407C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496046 | |||||||
| chr11:47496348 | G | A | 24 | a0001c0001t0001g0018 a0001c0001t0001g0137 a0001c0001t0001g0139 others(21): Show |
24 | HG00544.hp1 HG02083.hp1 HG02148.hp1 others(21): Show |
intron_variant | MODIFIER | c.71+3105C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496348 | |||||||
| chr11:47496649 | C | T | 1 | a0001c0001t0023g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.71+2804G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496649 | |||||||
| chr11:47496769 | A | T | 1 | a0001c0001t0002g0270 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.71+2684T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496769 | |||||||
| chr11:47496800 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+2653G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47496800 | |||||||
| chr11:47497004 | T | C | 2 | a0001c0001t0002g0290 a0001c0001t0025g0284 |
2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.71+2449A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497004 | |||||||
| chr11:47497123 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71+2330C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497123 | |||||||
| chr11:47497607 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.71+1846A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497607 | |||||||
| chr11:47497733 | G | A | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+1720C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47497733 | |||||||
| chr11:47498022 | C | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.71+1431G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498022 | |||||||
| chr11:47498229 | A | G | 1 | a0001c0001t0003g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71+1224T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498229 | |||||||
| chr11:47498242 | ACAAAAAG others(2): Show |
A | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.71+1202_71+1210del others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498242 | |||||||
| chr11:47498768 | G | C | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG02257.hp2 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71+685C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498768 | |||||||
| chr11:47498932 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0083 |
2 | HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.71+521G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47498932 | |||||||
| chr11:47499201 | A | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.71+252T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 3/14 | chr11 | 47499201 | |||||||
| chr11:47499773 | G | C | 2 | a0001c0001t0003g0065 a0001c0001t0003g0103 |
2 | NA18990.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-81-169C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47499773 | |||||||
| chr11:47500005 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-81-401G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500005 | |||||||
| chr11:47500265 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-82+596A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500265 | |||||||
| chr11:47500393 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+468G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500393 | |||||||
| chr11:47500424 | T | C | 1 | a0001c0001t0018g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-82+437A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500424 | |||||||
| chr11:47500512 | T | C | 1 | a0001c0001t0018g0138 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-82+349A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500512 | |||||||
| chr11:47500762 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0160 others(1): Show |
4 | HG02083.hp1 HG03831.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-82+99C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 2/14 | chr11 | 47500762 | |||||||
| chr11:47500936 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-153-4G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47500936 | |||||||
| chr11:47501117 | T | A | 3 | a0001c0001t0007g0016 a0001c0001t0007g0119 a0001c0001t0007g0211 |
3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-185A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501117 | |||||||
| chr11:47501162 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-153-230A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501162 | |||||||
| chr11:47501257 | G | C | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-153-325C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501257 | |||||||
| chr11:47501322 | CAGA | C | 75 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(72): Show |
75 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-153-393_-153-391d others(5): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501322 | |||||||
| chr11:47501586 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-654C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501586 | |||||||
| chr11:47501662 | C | A | 78 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(75): Show |
78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-153-730G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501662 | |||||||
| chr11:47501662 | CA | C | 14 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0136 others(11): Show |
14 | HG02071.hp2 HG02523.hp1 NA18982.hp2 others(11): Show |
intron_variant | MODIFIER | c.-153-731delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501662 | |||||||
| chr11:47501910 | T | G | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-153-978A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47501910 | |||||||
| chr11:47502026 | G | A | 1 | a0001c0001t0003g0087 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-153-1094C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502026 | |||||||
| chr11:47502037 | C | T | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-153-1105G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502037 | |||||||
| chr11:47502075 | T | C | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-153-1143A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502075 | |||||||
| chr11:47502289 | G | T | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-153-1357C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502289 | |||||||
| chr11:47502301 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-1369G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502301 | |||||||
| chr11:47502444 | A | T | 4 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(1): Show |
4 | HG03942.hp1 NA18952.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-1512T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502444 | |||||||
| chr11:47502558 | C | A | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-1626G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502558 | |||||||
| chr11:47502605 | G | T | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-153-1673C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502605 | |||||||
| chr11:47502620 | C | A | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-153-1688G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502620 | |||||||
| chr11:47502658 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-153-1726G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502658 | |||||||
| chr11:47502696 | G | A | 1 | a0001c0001t0003g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-153-1764C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502696 | |||||||
| chr11:47502764 | G | A | 1 | a0001c0001t0002g0257 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-153-1832C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502764 | |||||||
| chr11:47502765 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-1833C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502765 | |||||||
| chr11:47502769 | T | C | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | NA19056.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-153-1837A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502769 | |||||||
| chr11:47502788 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-153-1856G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502788 | |||||||
| chr11:47502846 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-153-1914A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502846 | |||||||
| chr11:47502847 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-153-1915T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502847 | |||||||
| chr11:47502905 | G | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-1973C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502905 | |||||||
| chr11:47502978 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-153-2046T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47502978 | |||||||
| chr11:47503023 | C | G | 2 | a0001c0001t0012g0251 a0001c0001t0012g0258 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-153-2091G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503023 | |||||||
| chr11:47503118 | G | C | 1 | a0001c0001t0002g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-153-2186C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503118 | |||||||
| chr11:47503427 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-153-2495A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503427 | |||||||
| chr11:47503700 | T | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-2768A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503700 | |||||||
| chr11:47503831 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-2899A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47503831 | |||||||
| chr11:47504121 | A | G | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-153-3189T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504121 | |||||||
| chr11:47504175 | A | AAAAC | 4 | a0001c0001t0002g0276 a0001c0001t0002g0279 a0001c0001t0002g0280 others(1): Show |
4 | HG03704.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-3247_-153-324 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504175 | |||||||
| chr11:47504452 | C | A | 1 | a0001c0001t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-153-3520G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504452 | |||||||
| chr11:47504500 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-153-3568G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504500 | |||||||
| chr11:47504552 | ATGGGCAA others(1843): Show |
A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-5470_-153-362 others(4): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504552 | |||||||
| chr11:47504601 | T | TA | 5 | a0001c0001t0001g0144 a0001c0001t0005g0021 a0001c0001t0005g0183 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-3670dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504601 | |||||||
| chr11:47504626 | C | A | 21 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0112 others(18): Show |
21 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.-153-3694G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504626 | |||||||
| chr11:47504718 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-153-3786T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504718 | |||||||
| chr11:47504728 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-153-3796G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504728 | |||||||
| chr11:47504902 | C | CA | 113 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0001g0173 others(110): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.-153-3971dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504902 | |||||||
| chr11:47504902 | C | CAA | 19 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(16): Show |
19 | HG02145.hp1 HG02486.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.-153-3972_-153-397 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47504902 | |||||||
| chr11:47505304 | T | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-4372A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505304 | |||||||
| chr11:47505440 | T | A | 2 | a0001c0001t0002g0290 a0001c0001t0025g0284 |
2 | NA18949.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-153-4508A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505440 | |||||||
| chr11:47505500 | G | T | 87 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(84): Show |
88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-153-4568C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505500 | |||||||
| chr11:47505569 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-4637C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505569 | |||||||
| chr11:47505643 | CA | C | 161 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(158): Show |
161 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-153-4712delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505643 | |||||||
| chr11:47505716 | C | T | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
7 | HG02809.hp2 HG02897.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-4784G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505716 | |||||||
| chr11:47505840 | C | T | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-153-4908G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505840 | |||||||
| chr11:47505936 | C | CA | 106 | a0001c0001t0001g0201 a0001c0001t0002g0011 a0001c0001t0002g0012 others(103): Show |
106 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-153-5005dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47505936 | |||||||
| chr11:47506074 | A | T | 6 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-5142T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506074 | |||||||
| chr11:47506081 | T | C | 1 | a0001c0001t0003g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-153-5149A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506081 | |||||||
| chr11:47506243 | G | A | 25 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-153-5311C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506243 | |||||||
| chr11:47506286 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-5354G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506286 | |||||||
| chr11:47506437 | GA | G | 8 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0163 others(5): Show |
8 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-5506delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506437 | |||||||
| chr11:47506563 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-5631C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47506563 | |||||||
| chr11:47507016 | C | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-6084G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507016 | |||||||
| chr11:47507413 | A | G | 3 | a0001c0001t0003g0067 a0001c0001t0003g0071 a0001c0001t0003g0073 |
3 | NA18747.hp1 NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-153-6481T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507413 | |||||||
| chr11:47507462 | A | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-6530T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507462 | |||||||
| chr11:47507485 | G | A | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-153-6553C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47507485 | |||||||
| chr11:47508072 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-7140T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508072 | |||||||
| chr11:47508203 | T | C | 1 | a0001c0001t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-153-7271A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508203 | |||||||
| chr11:47508297 | T | A | 14 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0136 others(11): Show |
14 | HG02071.hp2 HG02523.hp1 NA18982.hp2 others(11): Show |
intron_variant | MODIFIER | c.-153-7365A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508297 | |||||||
| chr11:47508395 | C | A | 98 | a0001c0001t0001g0098 a0001c0001t0002g0028 a0001c0001t0002g0029 others(95): Show |
99 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-153-7463G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508395 | |||||||
| chr11:47508472 | G | A | 81 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(78): Show |
81 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-153-7540C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508472 | |||||||
| chr11:47508569 | TAA | T | 144 | a0001c0001t0001g0018 a0001c0001t0001g0197 a0001c0001t0001g0319 others(141): Show |
145 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-153-7639_-153-763 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508569 | |||||||
| chr11:47508569 | TAAA | T | 181 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(178): Show |
181 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-153-7640_-153-763 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508569 | |||||||
| chr11:47508667 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-7735T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508667 | |||||||
| chr11:47508675 | A | AAC | 119 | a0001c0001t0001g0139 a0001c0001t0001g0201 a0001c0001t0002g0011 others(116): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-153-7745_-153-774 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508675 | |||||||
| chr11:47508697 | C | T | 1 | a0001c0001t0019g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-153-7765G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508697 | |||||||
| chr11:47508703 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-7771A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508703 | |||||||
| chr11:47508977 | C | T | 1 | a0001c0001t0002g0267 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-153-8045G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47508977 | |||||||
| chr11:47509014 | C | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8082G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509014 | |||||||
| chr11:47509021 | C | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8089G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509021 | |||||||
| chr11:47509044 | T | G | 1 | a0001c0001t0001g0336 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-153-8112A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509044 | |||||||
| chr11:47509084 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-153-8152A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509084 | |||||||
| chr11:47509257 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-153-8325C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509257 | |||||||
| chr11:47509283 | G | A | 3 | a0001c0001t0002g0283 a0001c0001t0002g0286 a0001c0001t0002g0289 |
3 | NA18956.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-153-8351C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509283 | |||||||
| chr11:47509445 | T | C | 3 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0325 |
3 | HG03041.hp2 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-153-8513A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509445 | |||||||
| chr11:47509509 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-8577C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509509 | |||||||
| chr11:47509801 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-8869G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509801 | |||||||
| chr11:47509897 | C | CA | 160 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(157): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-153-8966dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | |||||||
| chr11:47509897 | C | CAA | 151 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0001g0134 others(148): Show |
151 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-153-8967_-153-896 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | |||||||
| chr11:47509897 | C | CAAA | 7 | a0001c0001t0002g0231 a0001c0001t0002g0244 a0001c0001t0002g0252 others(4): Show |
7 | HG02257.hp1 HG02683.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-8968_-153-896 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509897 | |||||||
| chr11:47509914 | T | A | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-153-8982A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47509914 | |||||||
| chr11:47510011 | G | A | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-153-9079C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510011 | |||||||
| chr11:47510332 | T | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-153-9400A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510332 | |||||||
| chr11:47510644 | G | A | 2 | a0001c0001t0003g0036 a0001c0001t0003g0044 |
2 | HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-153-9712C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510644 | |||||||
| chr11:47510659 | G | A | 1 | a0001c0001t0004g0001 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-153-9727C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510659 | |||||||
| chr11:47510843 | T | G | 60 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(57): Show |
60 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-153-9911A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510843 | |||||||
| chr11:47510856 | G | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-9924C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510856 | |||||||
| chr11:47510861 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-9929C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510861 | |||||||
| chr11:47510953 | G | C | 1 | a0001c0001t0019g0182 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-153-10021C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47510953 | |||||||
| chr11:47511100 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-10168A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511100 | |||||||
| chr11:47511333 | C | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0083 |
2 | HG01361.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-153-10401G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511333 | |||||||
| chr11:47511743 | C | G | 2 | a0001c0001t0008g0089 a0001c0001t0008g0099 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-10811G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511743 | |||||||
| chr11:47511818 | A | AG | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-10887dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511818 | |||||||
| chr11:47511883 | C | G | 1 | a0001c0001t0002g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-153-10951G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511883 | |||||||
| chr11:47511886 | T | C | 9 | a0001c0001t0002g0310 a0001c0001t0002g0311 a0001c0001t0002g0312 others(6): Show |
9 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-10954A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511886 | |||||||
| chr11:47511900 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-153-10968C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511900 | |||||||
| chr11:47511931 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-153-10999G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47511931 | |||||||
| chr11:47512148 | G | A | 2 | a0001c0001t0008g0089 a0001c0001t0008g0099 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-11216C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512148 | |||||||
| chr11:47512166 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-11234C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512166 | |||||||
| chr11:47512167 | T | G | 1 | a0001c0001t0002g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-11235A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512167 | |||||||
| chr11:47512173 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-11241C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512173 | |||||||
| chr11:47512204 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0178 |
2 | NA19004.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-153-11272C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512204 | |||||||
| chr11:47512207 | C | T | 1 | a0001c0001t0002g0217 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-153-11275G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512207 | |||||||
| chr11:47512372 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-153-11440G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512372 | |||||||
| chr11:47512399 | T | C | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-153-11467A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512399 | |||||||
| chr11:47512452 | AT | A | 285 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(282): Show |
286 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.-153-11521delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512452 | |||||||
| chr11:47512452 | ATT | A | 14 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0160 others(11): Show |
14 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-153-11522_-153-11 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512452 | |||||||
| chr11:47512584 | C | A | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-11652G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512584 | |||||||
| chr11:47512951 | T | G | 1 | a0001c0001t0002g0252 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-153-12019A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47512951 | |||||||
| chr11:47513085 | A | G | 1 | a0001c0001t0003g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-12153T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513085 | |||||||
| chr11:47513408 | GT | G | 3 | a0001c0001t0002g0224 a0001c0001t0010g0101 a0001c0001t0010g0102 |
3 | HG02165.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-153-12477delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513408 | |||||||
| chr11:47513412 | T | C | 108 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-153-12480A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513412 | |||||||
| chr11:47513412 | T | TC | 8 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0163 others(5): Show |
8 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-12481dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513412 | |||||||
| chr11:47513413 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-153-12481G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513413 | |||||||
| chr11:47513461 | CCT | C | 78 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(75): Show |
78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-153-12531_-153-12 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513461 | |||||||
| chr11:47513580 | C | A | 1 | a0001c0001t0002g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-153-12648G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513580 | |||||||
| chr11:47513584 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-153-12652G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513584 | |||||||
| chr11:47513665 | C | T | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-153-12733G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513665 | |||||||
| chr11:47513792 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0160 |
2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-153-12860C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513792 | |||||||
| chr11:47513930 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-12998G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513930 | |||||||
| chr11:47513931 | C | CT | 19 | a0001c0001t0001g0319 a0001c0001t0001g0322 a0001c0001t0001g0323 others(16): Show |
19 | HG00673.hp2 HG02451.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.-153-13000dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | |||||||
| chr11:47513931 | C | CTT | 200 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(197): Show |
201 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-153-13001_-153-13 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | |||||||
| chr11:47513931 | C | CTTT | 78 | a0001c0001t0001g0172 a0001c0001t0002g0024 a0001c0001t0002g0025 others(75): Show |
78 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-153-13002_-153-13 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | |||||||
| chr11:47513931 | C | CTTTT | 28 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-153-13003_-153-13 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | |||||||
| chr11:47513931 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-153-12999G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513931 | |||||||
| chr11:47513941 | T | TTTC | 6 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0002g0230 others(3): Show |
6 | HG01169.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-13010_-153-13 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513941 | |||||||
| chr11:47513992 | G | C | 1 | a0001c0001t0002g0281 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-153-13060C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47513992 | |||||||
| chr11:47514116 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-153-13184C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514116 | |||||||
| chr11:47514144 | G | A | 6 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-13212C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514144 | |||||||
| chr11:47514164 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-153-13232T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514164 | |||||||
| chr11:47514250 | A | G | 1 | a0001c0001t0027g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-153-13318T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514250 | |||||||
| chr11:47514297 | A | T | 7 | a0001c0001t0003g0023 a0001c0001t0003g0046 a0001c0001t0003g0047 others(4): Show |
7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-13365T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514297 | |||||||
| chr11:47514304 | T | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-13372A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514304 | |||||||
| chr11:47514685 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-13753T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514685 | |||||||
| chr11:47514692 | C | CA | 123 | a0001c0001t0001g0019 a0001c0001t0001g0153 a0001c0001t0001g0179 others(120): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-153-13761dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514692 | |||||||
| chr11:47514692 | C | CAA | 106 | a0001c0001t0001g0098 a0001c0001t0001g0191 a0001c0001t0001g0199 others(103): Show |
107 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-153-13762_-153-13 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514692 | |||||||
| chr11:47514729 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-13797C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514729 | |||||||
| chr11:47514875 | A | T | 1 | a0001c0001t0002g0259 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-153-13943T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514875 | |||||||
| chr11:47514940 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-153-14008C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514940 | |||||||
| chr11:47514942 | A | G | 2 | a0001c0001t0008g0089 a0001c0001t0008g0099 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-153-14010T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47514942 | |||||||
| chr11:47515068 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-14136A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515068 | |||||||
| chr11:47515099 | G | T | 2 | a0001c0001t0002g0247 a0001c0001t0002g0267 |
2 | NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-153-14167C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515099 | |||||||
| chr11:47515301 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-153-14369C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515301 | |||||||
| chr11:47515426 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-14494T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515426 | |||||||
| chr11:47515578 | A | C | 3 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0295 |
3 | NA19065.hp2 NA19074.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-153-14646T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515578 | |||||||
| chr11:47515919 | C | CTTAT | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-14991_-153-14 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515919 | |||||||
| chr11:47515981 | A | G | 12 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(9): Show |
12 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-153-15049T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515981 | |||||||
| chr11:47515990 | C | T | 6 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-15058G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47515990 | |||||||
| chr11:47516106 | G | A | 6 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-15174C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516106 | |||||||
| chr11:47516138 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-15206T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516138 | |||||||
| chr11:47516231 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-15299G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516231 | |||||||
| chr11:47516501 | G | A | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-15569C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516501 | |||||||
| chr11:47516550 | T | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-15618A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516550 | |||||||
| chr11:47516582 | T | A | 1 | a0001c0001t0003g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-15650A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516582 | |||||||
| chr11:47516611 | T | G | 5 | a0001c0001t0001g0319 a0001c0001t0001g0330 a0001c0001t0024g0320 others(2): Show |
5 | HG02451.hp1 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153-15679A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516611 | |||||||
| chr11:47516612 | T | G | 1 | a0001c0001t0002g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-153-15680A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516612 | |||||||
| chr11:47516896 | C | A | 1 | a0001c0001t0002g0317 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-153-15964G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47516896 | |||||||
| chr11:47517037 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-153-16105T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517037 | |||||||
| chr11:47517124 | G | A | 1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-153-16192C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517124 | |||||||
| chr11:47517159 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-153-16227T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517159 | |||||||
| chr11:47517260 | G | GA | 43 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(40): Show |
43 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.-153-16329dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | |||||||
| chr11:47517260 | GA | G | 99 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-153-16329delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | |||||||
| chr11:47517260 | GAA | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0150 others(4): Show |
7 | HG02083.hp1 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-16330_-153-16 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | |||||||
| chr11:47517260 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0002g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-153-16338_-153-16 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517260 | |||||||
| chr11:47517261 | A | G | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG00597.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-153-16329T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517261 | |||||||
| chr11:47517656 | A | G | 99 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-153-16724T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517656 | |||||||
| chr11:47517656 | A | T | 6 | a0001c0001t0001g0140 a0001c0001t0002g0217 a0001c0001t0002g0218 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-16724T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517656 | |||||||
| chr11:47517657 | T | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA19062.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-153-16725A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517657 | |||||||
| chr11:47517714 | GC | G | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-153-16783delG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517714 | |||||||
| chr11:47517729 | T | C | 3 | a0001c0001t0007g0016 a0001c0001t0007g0119 a0001c0001t0007g0211 |
3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-16797A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517729 | |||||||
| chr11:47517967 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-17035A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47517967 | |||||||
| chr11:47518145 | T | C | 77 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(74): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-153-17213A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518145 | |||||||
| chr11:47518440 | C | G | 1 | a0001c0001t0005g0021 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-153-17508G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518440 | |||||||
| chr11:47518455 | C | T | 209 | a0001c0001t0001g0098 a0001c0001t0002g0011 a0001c0001t0002g0012 others(206): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-153-17523G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518455 | |||||||
| chr11:47518765 | G | C | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
7 | HG02809.hp2 HG02897.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-17833C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518765 | |||||||
| chr11:47518800 | C | T | 1 | a0001c0001t0006g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-153-17868G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518800 | |||||||
| chr11:47518947 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0153 a0001c0001t0001g0155 others(1): Show |
4 | NA18988.hp2 NA18989.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-153-18015A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47518947 | |||||||
| chr11:47519153 | G | T | 1 | a0001c0001t0003g0014 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-153-18221C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519153 | |||||||
| chr11:47519285 | C | G | 2 | a0001c0001t0002g0110 a0001c0001t0002g0112 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-153-18353G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519285 | |||||||
| chr11:47519350 | G | A | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-153-18418C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519350 | |||||||
| chr11:47519437 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-18505T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519437 | |||||||
| chr11:47519453 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-18521G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519453 | |||||||
| chr11:47519479 | C | CTAAA | 27 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0147 others(24): Show |
27 | HG00639.hp2 HG01258.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-153-18551_-153-18 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | |||||||
| chr11:47519479 | C | CTAAATAA others(1): Show |
3 | a0001c0001t0001g0187 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG02559.hp1 NA18953.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-153-18555_-153-18 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | |||||||
| chr11:47519479 | CTAAA | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(93): Show |
97 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-153-18551_-153-18 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | |||||||
| chr11:47519479 | CTAAATAA others(1): Show |
C | 28 | a0001c0001t0001g0204 a0001c0001t0002g0011 a0001c0001t0002g0012 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-153-18555_-153-18 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | |||||||
| chr11:47519479 | CTAAATAA others(5): Show |
C | 76 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0002g0227 others(73): Show |
76 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-153-18559_-153-18 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519479 | |||||||
| chr11:47519508 | T | G | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-153-18576A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519508 | |||||||
| chr11:47519512 | T | G | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-153-18580A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519512 | |||||||
| chr11:47519592 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-153-18660C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519592 | |||||||
| chr11:47519597 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-153-18665C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519597 | |||||||
| chr11:47519840 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0030 |
2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-153-18908C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519840 | |||||||
| chr11:47519842 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-18910C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519842 | |||||||
| chr11:47519938 | T | TA | 87 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(84): Show |
88 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-153-19007dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47519938 | |||||||
| chr11:47520010 | T | TA | 332 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(329): Show |
333 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.-153-19079dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520010 | |||||||
| chr11:47520027 | A | AG | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0162 |
3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-19096dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520027 | |||||||
| chr11:47520109 | G | C | 1 | a0001c0001t0003g0086 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-153-19177C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520109 | |||||||
| chr11:47520229 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-153-19297A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520229 | |||||||
| chr11:47520306 | GATACA | G | 3 | a0001c0001t0002g0025 a0001c0001t0002g0236 a0001c0001t0003g0051 |
3 | HG03834.hp2 NA18942.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-153-19379_-153-19 others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520306 | |||||||
| chr11:47520765 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-19833A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520765 | |||||||
| chr11:47520821 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-19889G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520821 | |||||||
| chr11:47520836 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-19904C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47520836 | |||||||
| chr11:47521079 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-20147T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521079 | |||||||
| chr11:47521204 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-20272C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521204 | |||||||
| chr11:47521207 | G | A | 9 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(6): Show |
9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-20275C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521207 | |||||||
| chr11:47521576 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-153-20644G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521576 | |||||||
| chr11:47521597 | A | G | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-20665T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521597 | |||||||
| chr11:47521769 | A | C | 1 | a0001c0001t0003g0050 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-153-20837T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521769 | |||||||
| chr11:47521913 | A | AT | 108 | a0001c0001t0001g0153 a0001c0001t0001g0177 a0001c0001t0001g0189 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-153-20982dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521913 | |||||||
| chr11:47521915 | T | G | 1 | a0001c0001t0003g0046 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-153-20983A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47521915 | |||||||
| chr11:47522213 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-153-21281C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522213 | |||||||
| chr11:47522310 | G | A | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-21378C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522310 | |||||||
| chr11:47522322 | T | TG | 3 | a0001c0001t0001g0135 a0001c0001t0010g0101 a0001c0001t0010g0102 |
3 | HG02896.hp2 HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-153-21391dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522322 | |||||||
| chr11:47522355 | A | G | 3 | a0001c0001t0007g0016 a0001c0001t0007g0119 a0001c0001t0007g0211 |
3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-153-21423T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522355 | |||||||
| chr11:47522422 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0197 |
2 | NA18970.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-153-21490G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522422 | |||||||
| chr11:47522461 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-153-21529T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522461 | |||||||
| chr11:47522523 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-21591G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522523 | |||||||
| chr11:47522538 | C | A | 1 | a0001c0001t0002g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-153-21606G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522538 | |||||||
| chr11:47522541 | C | A | 328 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(325): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.-153-21609G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522541 | |||||||
| chr11:47522702 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-21770A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522702 | |||||||
| chr11:47522781 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-153-21849C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522781 | |||||||
| chr11:47522828 | G | GA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0203 a0001c0001t0002g0244 others(5): Show |
8 | HG01192.hp2 HG02109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-153-21897dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47522828 | |||||||
| chr11:47523069 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-153-22137T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523069 | |||||||
| chr11:47523105 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-22173T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523105 | |||||||
| chr11:47523235 | G | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-153-22303C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523235 | |||||||
| chr11:47523299 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-153-22367T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523299 | |||||||
| chr11:47523415 | C | T | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-153-22483G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523415 | |||||||
| chr11:47523522 | A | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-22590T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523522 | |||||||
| chr11:47523616 | A | G | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0198 others(1): Show |
4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-153-22684T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523616 | |||||||
| chr11:47523673 | T | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-153-22741A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523673 | |||||||
| chr11:47523820 | A | C | 1 | a0001c0001t0003g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-153-22888T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523820 | |||||||
| chr11:47523959 | G | A | 3 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-153-23027C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523959 | |||||||
| chr11:47523970 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-153-23038A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47523970 | |||||||
| chr11:47524145 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-153-23213T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524145 | |||||||
| chr11:47524317 | C | A | 1 | a0001c0001t0003g0046 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-153-23385G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524317 | |||||||
| chr11:47524488 | C | CT | 4 | a0001c0001t0002g0276 a0001c0001t0002g0279 a0001c0001t0002g0280 others(1): Show |
4 | HG03704.hp2 HG03834.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-23557dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524488 | |||||||
| chr11:47524530 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-153-23598G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524530 | |||||||
| chr11:47524986 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-153-24054C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47524986 | |||||||
| chr11:47525253 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-153-24321T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525253 | |||||||
| chr11:47525390 | CCAA | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | NA18961.hp1 NA18972.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-24461_-153-24 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525390 | |||||||
| chr11:47525494 | T | C | 78 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(75): Show |
78 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-153-24562A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525494 | |||||||
| chr11:47525628 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-153-24696G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525628 | |||||||
| chr11:47525726 | C | T | 1 | a0001c0001t0003g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-153-24794G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525726 | |||||||
| chr11:47525861 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-153-24929G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525861 | |||||||
| chr11:47525928 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0056 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-153-25009_-153-24 others(19): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525928 | |||||||
| chr11:47525940 | CA | C | 313 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(310): Show |
314 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.-153-25009delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47525940 | |||||||
| chr11:47526142 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-153-25210G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526142 | |||||||
| chr11:47526182 | AGCCAGGT others(12): Show |
A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0162 |
3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-153-25269_-153-25 others(25): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526182 | |||||||
| chr11:47526262 | G | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0108 a0001c0002t0002g0299 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25330C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526262 | |||||||
| chr11:47526485 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25553A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526485 | |||||||
| chr11:47526561 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-153-25629G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526561 | |||||||
| chr11:47526609 | T | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-25677A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526609 | |||||||
| chr11:47526656 | A | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0130 |
2 | HG01099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-153-25724T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526656 | |||||||
| chr11:47526766 | C | T | 20 | a0001c0001t0003g0014 a0001c0001t0003g0035 a0001c0001t0003g0040 others(17): Show |
20 | HG00673.hp2 HG00735.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-153-25834G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526766 | |||||||
| chr11:47526822 | C | T | 2 | a0001c0001t0002g0315 a0001c0001t0003g0046 |
2 | HG00280.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-153-25890G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526822 | |||||||
| chr11:47526907 | T | C | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-25975A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47526907 | |||||||
| chr11:47527050 | T | TA | 13 | a0001c0001t0001g0137 a0001c0001t0001g0159 a0001c0001t0002g0105 others(10): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+25941dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527050 | |||||||
| chr11:47527068 | T | C | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+25924A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527068 | |||||||
| chr11:47527216 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-154+25776A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527216 | |||||||
| chr11:47527218 | A | G | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+25774T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527218 | |||||||
| chr11:47527248 | G | A | 9 | a0001c0001t0001g0144 a0001c0001t0001g0158 a0001c0001t0001g0163 others(6): Show |
9 | HG01261.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+25744C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527248 | |||||||
| chr11:47527724 | T | C | 6 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+25268A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47527724 | |||||||
| chr11:47528101 | C | T | 2 | a0001c0001t0003g0035 a0001c0001t0028g0034 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+24891G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528101 | |||||||
| chr11:47528208 | A | G | 3 | a0001c0001t0002g0076 a0001c0001t0003g0075 a0001c0001t0003g0078 |
3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-154+24784T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528208 | |||||||
| chr11:47528434 | A | G | 1 | a0001c0001t0002g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-154+24558T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528434 | |||||||
| chr11:47528446 | A | AT | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+24545dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528446 | |||||||
| chr11:47528453 | T | G | 1 | a0001c0001t0006g0111 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-154+24539A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528453 | |||||||
| chr11:47528890 | C | CA | 108 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(105): Show |
108 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-154+24101dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47528890 | |||||||
| chr11:47529005 | A | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0279 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-154+23987T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529005 | |||||||
| chr11:47529077 | C | CT | 12 | a0001c0001t0001g0026 a0001c0001t0001g0137 a0001c0001t0001g0191 others(9): Show |
12 | HG01346.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-154+23914dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529077 | |||||||
| chr11:47529139 | G | A | 2 | a0001c0001t0002g0277 a0001c0001t0002g0292 |
2 | HG00544.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-154+23853C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529139 | |||||||
| chr11:47529166 | C | T | 3 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0004 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+23826G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529166 | |||||||
| chr11:47529188 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+23804G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529188 | |||||||
| chr11:47529254 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+23738A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529254 | |||||||
| chr11:47529283 | GGGGACA | G | 77 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(74): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+23703_-154+23 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529283 | |||||||
| chr11:47529695 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+23297G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529695 | |||||||
| chr11:47529827 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-154+23165C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529827 | |||||||
| chr11:47529914 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+23078G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47529914 | |||||||
| chr11:47530087 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-154+22905C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530087 | |||||||
| chr11:47530502 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-154+22490A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530502 | |||||||
| chr11:47530623 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-154+22369C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530623 | |||||||
| chr11:47530749 | G | GT | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+22242dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530749 | |||||||
| chr11:47530882 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+22110C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530882 | |||||||
| chr11:47530906 | A | AC | 3 | a0001c0001t0002g0234 a0001c0001t0002g0235 a0001c0001t0002g0271 |
3 | NA18985.hp2 NA19007.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-154+22085_-154+22 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530906 | |||||||
| chr11:47530934 | C | A | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+22058G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47530934 | |||||||
| chr11:47531027 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-154+21965G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531027 | |||||||
| chr11:47531180 | G | A | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-154+21812C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531180 | |||||||
| chr11:47531265 | C | A | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-154+21727G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531265 | |||||||
| chr11:47531272 | C | CA | 22 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(19): Show |
23 | HG01884.hp1 HG02055.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.-154+21719dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531272 | |||||||
| chr11:47531298 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0191 |
3 | NA18945.hp1 NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-154+21694C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531298 | |||||||
| chr11:47531474 | TAGG | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0198 others(1): Show |
4 | HG00558.hp2 NA18964.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-154+21515_-154+21 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531474 | |||||||
| chr11:47531526 | A | T | 1 | a0001c0001t0003g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-154+21466T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531526 | |||||||
| chr11:47531567 | T | TCAAA | 320 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(317): Show |
321 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(318): Show |
intron_variant | MODIFIER | c.-154+21421_-154+21 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531567 | |||||||
| chr11:47531567 | T | TCAAACAA others(1): Show |
13 | a0001c0001t0001g0026 a0001c0001t0002g0108 a0001c0001t0002g0217 others(10): Show |
13 | HG00280.hp2 HG01243.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+21417_-154+21 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47531567 | |||||||
| chr11:47532035 | A | AT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0128 others(9): Show |
12 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+20956dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532035 | |||||||
| chr11:47532040 | T | A | 1 | a0001c0001t0003g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+20952A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532040 | |||||||
| chr11:47532041 | T | A | 3 | a0001c0001t0001g0152 a0001c0001t0003g0035 a0001c0001t0028g0034 |
3 | HG00735.hp2 HG01175.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-154+20951A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532041 | |||||||
| chr11:47532053 | CAG | C | 3 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0081 |
3 | HG03710.hp1 HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-154+20937_-154+20 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532053 | |||||||
| chr11:47532117 | G | A | 10 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(7): Show |
10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+20875C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532117 | |||||||
| chr11:47532208 | G | T | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+20784C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532208 | |||||||
| chr11:47532211 | A | G | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+20781T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532211 | |||||||
| chr11:47532361 | T | C | 1 | a0001c0001t0027g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-154+20631A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532361 | |||||||
| chr11:47532505 | C | G | 330 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(327): Show |
331 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.-154+20487G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532505 | |||||||
| chr11:47532505 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0176 a0001c0001t0001g0180 |
3 | NA18983.hp2 NA19083.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-154+20487G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532505 | |||||||
| chr11:47532785 | G | A | 108 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+20207C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47532785 | |||||||
| chr11:47533023 | T | C | 1 | a0001c0001t0002g0307 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-154+19969A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533023 | |||||||
| chr11:47533092 | A | AT | 8 | a0001c0001t0001g0098 a0001c0001t0001g0212 a0001c0001t0001g0319 others(5): Show |
8 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+19899dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533092 | |||||||
| chr11:47533225 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19767C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533225 | |||||||
| chr11:47533237 | A | G | 3 | a0001c0001t0002g0231 a0001c0001t0002g0248 a0001c0001t0002g0265 |
3 | HG01071.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-154+19755T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533237 | |||||||
| chr11:47533346 | G | A | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-154+19646C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533346 | |||||||
| chr11:47533451 | C | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
105 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-154+19541G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533451 | |||||||
| chr11:47533631 | A | AATACATA others(5): Show |
1 | a0001c0001t0003g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-154+19360_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533631 | |||||||
| chr11:47533631 | A | ATAAATAC others(4): Show |
2 | a0001c0001t0003g0035 a0001c0001t0028g0034 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+19360_-154+19 others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533631 | |||||||
| chr11:47533635 | A | AATAAATA others(5): Show |
4 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0100 others(1): Show |
4 | NA18939.hp2 NA18953.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19356_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | AATAC | 4 | a0001c0001t0003g0078 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02148.hp2 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19353_-154+19 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | AATACATA others(1): Show |
244 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(241): Show |
245 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.-154+19349_-154+19 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | AATACATA others(5): Show |
63 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0002g0285 others(60): Show |
63 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-154+19345_-154+19 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | AATACATA others(9): Show |
3 | a0001c0001t0003g0049 a0001c0001t0003g0077 a0001c0001t0003g0085 |
3 | HG00323.hp1 HG01433.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-154+19341_-154+19 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | AATACATA others(13): Show |
7 | a0001c0001t0003g0023 a0001c0001t0003g0046 a0001c0001t0003g0047 others(4): Show |
7 | NA18944.hp1 NA18945.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+19337_-154+19 others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533635 | A | C | 5 | a0001c0001t0001g0319 a0001c0001t0003g0035 a0001c0001t0003g0060 others(2): Show |
5 | HG00558.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+19357T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533635 | |||||||
| chr11:47533716 | A | G | 3 | a0001c0001t0002g0231 a0001c0001t0002g0248 a0001c0001t0002g0265 |
3 | HG01071.hp1 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-154+19276T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533716 | |||||||
| chr11:47533779 | C | T | 105 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
105 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-154+19213G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533779 | |||||||
| chr11:47533804 | T | TA | 62 | a0001c0001t0001g0172 a0001c0001t0001g0335 a0001c0001t0001g0336 others(59): Show |
62 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-154+19187_-154+19 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533804 | |||||||
| chr11:47533804 | TCC | T | 15 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0322 others(12): Show |
15 | HG02486.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+19186_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533804 | |||||||
| chr11:47533805 | C | A | 260 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(257): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.-154+19187G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533805 | |||||||
| chr11:47533807 | C | A | 77 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0172 others(74): Show |
77 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+19185G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533807 | |||||||
| chr11:47533808 | C | A | 255 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(252): Show |
256 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-154+19184G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533808 | |||||||
| chr11:47533809 | C | A | 62 | a0001c0001t0001g0172 a0001c0001t0001g0335 a0001c0001t0001g0336 others(59): Show |
62 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-154+19183G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | |||||||
| chr11:47533809 | C | CAA | 27 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(24): Show |
27 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-154+19181_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | |||||||
| chr11:47533809 | CA | C | 113 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(110): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.-154+19182delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533809 | |||||||
| chr11:47533811 | A | C | 15 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0001g0322 others(12): Show |
15 | HG02486.hp2 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+19181T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533811 | |||||||
| chr11:47533812 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+19180T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533812 | |||||||
| chr11:47533814 | A | C | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-154+19178T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533814 | |||||||
| chr11:47533815 | A | C | 3 | a0001c0001t0024g0320 a0001c0003t0011g0308 a0001c0003t0011g0309 |
3 | HG02896.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+19177T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533815 | |||||||
| chr11:47533831 | A | AAG | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+19160_-154+19 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533831 | |||||||
| chr11:47533842 | T | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+19150A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47533842 | |||||||
| chr11:47534022 | C | CT | 100 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
101 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-154+18969dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | |||||||
| chr11:47534022 | C | CTT | 99 | a0001c0001t0001g0126 a0001c0001t0001g0137 a0001c0001t0001g0156 others(96): Show |
99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-154+18968_-154+18 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | |||||||
| chr11:47534022 | C | CTTT | 28 | a0001c0001t0002g0013 a0001c0001t0002g0116 a0001c0001t0002g0223 others(25): Show |
28 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-154+18967_-154+18 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | |||||||
| chr11:47534022 | C | T | 3 | a0001c0001t0024g0320 a0001c0003t0011g0308 a0001c0003t0011g0309 |
3 | HG02896.hp1 HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+18970G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534022 | |||||||
| chr11:47534045 | G | T | 1 | a0001c0001t0002g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-154+18947C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534045 | |||||||
| chr11:47534127 | C | G | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+18865G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534127 | |||||||
| chr11:47534198 | T | C | 1 | a0001c0001t0001g0339 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-154+18794A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534198 | |||||||
| chr11:47534232 | A | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+18760T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534232 | |||||||
| chr11:47534531 | C | A | 5 | a0001c0001t0006g0104 a0001c0001t0006g0111 a0001c0001t0006g0113 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+18461G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534531 | |||||||
| chr11:47534722 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-154+18270G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534722 | |||||||
| chr11:47534832 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+18160C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534832 | |||||||
| chr11:47534837 | G | C | 1 | a0001c0001t0002g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-154+18155C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534837 | |||||||
| chr11:47534996 | A | T | 3 | a0001c0001t0004g0002 a0001c0001t0004g0003 a0001c0001t0004g0004 |
3 | HG02818.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+17996T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47534996 | |||||||
| chr11:47535006 | C | T | 3 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0115 |
3 | HG00642.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-154+17986G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535006 | |||||||
| chr11:47535031 | G | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0249 |
2 | HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-154+17961C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535031 | |||||||
| chr11:47535348 | T | C | 9 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(6): Show |
9 | NA18947.hp1 NA18963.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+17644A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535348 | |||||||
| chr11:47535581 | G | A | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+17411C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535581 | |||||||
| chr11:47535608 | G | A | 8 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0115 others(5): Show |
8 | HG00323.hp2 HG00642.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+17384C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535608 | |||||||
| chr11:47535679 | C | CA | 12 | a0001c0001t0001g0191 a0001c0001t0001g0330 a0001c0001t0001g0334 others(9): Show |
12 | HG02257.hp2 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+17312dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535679 | |||||||
| chr11:47535679 | C | CAA | 9 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+17311_-154+17 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535679 | |||||||
| chr11:47535688 | A | T | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+17304T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535688 | |||||||
| chr11:47535692 | A | AT | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+17299_-154+17 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535692 | |||||||
| chr11:47535692 | A | T | 14 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0163 others(11): Show |
14 | HG00438.hp2 HG01243.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+17300T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535692 | |||||||
| chr11:47535693 | A | T | 1 | a0001c0001t0003g0065 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-154+17299T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535693 | |||||||
| chr11:47535696 | T | A | 15 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(12): Show |
15 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.-154+17296A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535696 | |||||||
| chr11:47535804 | C | T | 209 | a0001c0001t0001g0098 a0001c0001t0002g0011 a0001c0001t0002g0012 others(206): Show |
210 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.-154+17188G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535804 | |||||||
| chr11:47535908 | G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-154+17084C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535908 | |||||||
| chr11:47535950 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-154+17042C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47535950 | |||||||
| chr11:47536037 | T | C | 9 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+16955A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536037 | |||||||
| chr11:47536240 | C | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+16752G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536240 | |||||||
| chr11:47536309 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-154+16683A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536309 | |||||||
| chr11:47536319 | T | C | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+16673A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536319 | |||||||
| chr11:47536557 | T | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+16435A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536557 | |||||||
| chr11:47536668 | G | A | 73 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(70): Show |
73 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-154+16324C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536668 | |||||||
| chr11:47536757 | C | G | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+16235G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536757 | |||||||
| chr11:47536964 | C | T | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+16028G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47536964 | |||||||
| chr11:47537245 | A | AT | 19 | a0001c0001t0001g0098 a0001c0001t0001g0324 a0001c0001t0002g0230 others(16): Show |
19 | HG00642.hp1 HG00741.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-154+15746dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537245 | |||||||
| chr11:47537245 | AT | A | 105 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(102): Show |
105 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-154+15746delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537245 | |||||||
| chr11:47537265 | T | G | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-154+15727A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537265 | |||||||
| chr11:47537306 | G | A | 108 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+15686C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537306 | |||||||
| chr11:47537595 | AT | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+15396delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537595 | |||||||
| chr11:47537836 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-154+15156A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537836 | |||||||
| chr11:47537874 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+15118G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537874 | |||||||
| chr11:47537918 | CT | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0134 a0001c0001t0001g0319 others(6): Show |
9 | HG02258.hp2 HG02451.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+15073delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47537918 | |||||||
| chr11:47538210 | G | A | 1 | a0001c0001t0003g0015 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-154+14782C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538210 | |||||||
| chr11:47538250 | A | T | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-154+14742T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538250 | |||||||
| chr11:47538420 | G | A | 5 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0254 others(2): Show |
5 | HG00639.hp2 HG00735.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+14572C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538420 | |||||||
| chr11:47538539 | AGGCTGAG others(10): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-154+14436_-154+14 others(23): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538539 | |||||||
| chr11:47538555 | A | C | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+14437T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538555 | |||||||
| chr11:47538642 | C | CA | 175 | a0001c0001t0001g0098 a0001c0001t0002g0011 a0001c0001t0002g0012 others(172): Show |
175 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-154+14349dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538642 | |||||||
| chr11:47538642 | C | CAA | 8 | a0001c0001t0002g0227 a0001c0001t0002g0248 a0001c0001t0002g0290 others(5): Show |
8 | HG00438.hp2 HG00597.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+14348_-154+14 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538642 | |||||||
| chr11:47538655 | A | AT | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0188 |
3 | HG02083.hp1 NA18747.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-154+14336_-154+14 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538655 | |||||||
| chr11:47538659 | A | AT | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-154+14332_-154+14 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538659 | |||||||
| chr11:47538659 | A | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0188 |
3 | HG02083.hp1 NA18747.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-154+14333T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538659 | |||||||
| chr11:47538881 | T | C | 59 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+14111A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538881 | |||||||
| chr11:47538999 | T | C | 2 | a0001c0002t0002g0299 a0001c0002t0002g0300 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-154+13993A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47538999 | |||||||
| chr11:47539229 | T | TA | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+13762dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539229 | |||||||
| chr11:47539275 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-154+13717G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539275 | |||||||
| chr11:47539366 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-154+13626G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47539366 | |||||||
| chr11:47540132 | T | C | 1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-154+12860A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540132 | |||||||
| chr11:47540285 | T | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+12707A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540285 | |||||||
| chr11:47540313 | C | T | 3 | a0001c0001t0002g0076 a0001c0001t0003g0075 a0001c0001t0003g0078 |
3 | HG01943.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-154+12679G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540313 | |||||||
| chr11:47540505 | G | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+12487C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540505 | |||||||
| chr11:47540684 | G | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG01496.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+12308C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540684 | |||||||
| chr11:47540689 | C | T | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+12303G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540689 | |||||||
| chr11:47540885 | A | AAAC | 104 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(101): Show |
104 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-154+12104_-154+12 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540885 | |||||||
| chr11:47540885 | AAAC | A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0319 a0001c0001t0024g0320 others(2): Show |
5 | HG02293.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+12104_-154+12 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540885 | |||||||
| chr11:47540972 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+12020C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47540972 | |||||||
| chr11:47541292 | A | AC | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+11699dupG | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541292 | |||||||
| chr11:47541496 | G | GCCTGGCC others(25): Show |
1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-154+11464_-154+11 others(38): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541496 | |||||||
| chr11:47541684 | G | GTC | 51 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0027 others(48): Show |
51 | HG00741.hp1 HG01071.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.-154+11306_-154+11 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541684 | |||||||
| chr11:47541686 | C | CAAAGAAA others(5): Show |
2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-154+11294_-154+11 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | C | CG | 3 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0007g0211 |
3 | HG02055.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | C | CGAAAGAA others(87): Show |
1 | a0001c0001t0007g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-154+11305_-154+11 others(100): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | C | CGAAAGAA others(220): Show |
1 | a0001c0001t0007g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-154+11305_-154+11 others(233): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | C | CT | 29 | a0001c0001t0001g0026 a0001c0001t0001g0129 a0001c0001t0001g0130 others(26): Show |
29 | HG00597.hp2 HG01099.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | C | CTCA | 17 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG01192.hp1 HG01255.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-154+11305_-154+11 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | CAAAGAAA | C | 4 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0004 others(1): Show |
5 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11299_-154+11 others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541686 | CAAAGAAA others(8): Show |
C | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-154+11291_-154+11 others(21): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541686 | |||||||
| chr11:47541687 | A | C | 29 | a0001c0001t0001g0026 a0001c0001t0001g0129 a0001c0001t0001g0130 others(26): Show |
29 | HG00597.hp2 HG01099.hp1 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+11305T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541687 | |||||||
| chr11:47541687 | A | T | 224 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(221): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-154+11305T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541687 | |||||||
| chr11:47541688 | A | C | 224 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(221): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-154+11304T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541688 | |||||||
| chr11:47541689 | AG | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0124 a0001c0001t0001g0125 others(18): Show |
21 | HG00280.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-154+11302delC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541689 | |||||||
| chr11:47541690 | G | A | 300 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(297): Show |
300 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.-154+11302C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541690 | |||||||
| chr11:47541692 | AAGAAAGA others(95): Show |
A | 8 | a0001c0001t0001g0319 a0001c0001t0002g0274 a0001c0001t0002g0275 others(5): Show |
8 | HG01433.hp2 HG01517.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541692 | |||||||
| chr11:47541693 | AGAAAGAA others(82): Show |
A | 2 | a0001c0001t0002g0108 a0001c0001t0021g0082 |
2 | HG02293.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(95): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541693 | |||||||
| chr11:47541693 | AGAAAGAA others(94): Show |
A | 16 | a0001c0001t0002g0273 a0001c0001t0002g0276 a0001c0001t0002g0278 others(13): Show |
16 | HG00544.hp2 HG00621.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541693 | |||||||
| chr11:47541694 | G | A | 295 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(292): Show |
295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.-154+11298C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541694 | |||||||
| chr11:47541696 | AAGAAAGA others(91): Show |
A | 31 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0030 others(28): Show |
31 | HG00408.hp2 HG00438.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(104): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541696 | |||||||
| chr11:47541697 | AGAAAGAA others(78): Show |
A | 2 | a0001c0001t0002g0227 a0001c0001t0003g0058 |
2 | HG01975.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(91): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541697 | |||||||
| chr11:47541697 | AGAAAGAA others(90): Show |
A | 30 | a0001c0001t0002g0024 a0001c0001t0002g0226 a0001c0001t0002g0229 others(27): Show |
30 | HG00609.hp2 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(103): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541697 | |||||||
| chr11:47541698 | G | A | 232 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(229): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.-154+11294C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541698 | |||||||
| chr11:47541700 | AAGAAAGA others(87): Show |
A | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0230 others(2): Show |
5 | HG02559.hp1 HG04228.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(100): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541700 | |||||||
| chr11:47541701 | AGAAAGAA others(74): Show |
A | 4 | a0001c0001t0003g0045 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | HG02273.hp2 HG04115.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(87): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541701 | |||||||
| chr11:47541701 | AGAAAGAA others(86): Show |
A | 6 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0115 others(3): Show |
6 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+11198_-154+11 others(99): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541701 | |||||||
| chr11:47541702 | G | A | 162 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(159): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-154+11290C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541702 | |||||||
| chr11:47541705 | AGAAAGAA others(70): Show |
A | 2 | a0001c0001t0001g0323 a0001c0001t0013g0333 |
2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-154+11210_-154+11 others(83): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541705 | |||||||
| chr11:47541705 | AGAAAGAA others(81): Show |
A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0096 a0001c0001t0003g0216 |
3 | HG03239.hp2 NA18906.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(94): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541705 | |||||||
| chr11:47541706 | G | A | 19 | a0001c0001t0001g0026 a0001c0001t0001g0324 a0001c0001t0001g0325 others(16): Show |
19 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-154+11286C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541706 | |||||||
| chr11:47541707 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11285T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541707 | |||||||
| chr11:47541709 | AGAAAGAA others(77): Show |
A | 6 | a0001c0001t0002g0217 a0001c0001t0002g0305 a0001c0001t0002g0306 others(3): Show |
6 | HG00323.hp1 HG01257.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(90): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541709 | |||||||
| chr11:47541710 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11282C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541710 | |||||||
| chr11:47541712 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11280T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541712 | |||||||
| chr11:47541713 | AGAAAGAA others(73): Show |
A | 14 | a0001c0001t0001g0330 a0001c0001t0002g0076 a0001c0001t0002g0307 others(11): Show |
14 | HG00597.hp1 HG00642.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(86): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541713 | |||||||
| chr11:47541714 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11278C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541714 | |||||||
| chr11:47541717 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11275T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | |||||||
| chr11:47541717 | AGAAAGAA others(45): Show |
A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0163 a0001c0001t0001g0180 |
3 | HG01978.hp2 HG03486.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-154+11223_-154+11 others(58): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | |||||||
| chr11:47541717 | AGAAAGAA others(57): Show |
A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0128 others(22): Show |
25 | HG01081.hp2 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(70): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | |||||||
| chr11:47541717 | AGAAAGAA others(69): Show |
A | 20 | a0001c0001t0001g0151 a0001c0001t0001g0166 a0001c0001t0001g0173 others(17): Show |
20 | HG00673.hp2 HG00735.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(82): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541717 | |||||||
| chr11:47541718 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11274C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541718 | |||||||
| chr11:47541720 | A | C | 2 | a0001c0001t0004g0008 a0001c0001t0004g0009 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11272T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541720 | |||||||
| chr11:47541721 | AGAAAGAA others(29): Show |
A | 1 | a0001c0001t0001g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-154+11235_-154+11 others(42): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | |||||||
| chr11:47541721 | AGAAAGAA others(53): Show |
A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0124 a0001c0001t0001g0137 others(29): Show |
32 | HG00280.hp2 HG01175.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(66): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | |||||||
| chr11:47541721 | AGAAAGAA others(65): Show |
A | 33 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0001g0139 others(30): Show |
33 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(78): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541721 | |||||||
| chr11:47541723 | AAAGAACG others(32): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11230_-154+11 others(45): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541723 | |||||||
| chr11:47541724 | A | C | 1 | a0001c0001t0004g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-154+11268T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541724 | |||||||
| chr11:47541725 | AGAACGAA others(9): Show |
A | 4 | a0001c0001t0004g0001 a0001c0001t0004g0003 a0001c0001t0004g0004 others(1): Show |
5 | HG01884.hp1 HG02559.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11251_-154+11 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | |||||||
| chr11:47541725 | AGAACGAA others(49): Show |
A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0134 a0001c0001t0001g0144 others(10): Show |
13 | HG01081.hp1 HG01261.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(62): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | |||||||
| chr11:47541725 | AGAACGAA others(61): Show |
A | 61 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0027 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-154+11199_-154+11 others(74): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541725 | |||||||
| chr11:47541728 | ACGAAAGA others(79): Show |
A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-154+11178_-154+11 others(92): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541728 | |||||||
| chr11:47541729 | C | A | 9 | a0001c0001t0002g0116 a0001c0001t0004g0002 a0001c0001t0004g0006 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+11263G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541729 | |||||||
| chr11:47541732 | A | C | 3 | a0001c0001t0004g0002 a0001c0001t0004g0008 a0001c0001t0004g0009 |
3 | HG02055.hp1 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11260T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541732 | |||||||
| chr11:47541736 | A | C | 1 | a0001c0001t0004g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-154+11256T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541736 | |||||||
| chr11:47541740 | A | C | 1 | a0001c0001t0004g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-154+11252T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541740 | |||||||
| chr11:47541741 | C | A | 9 | a0001c0001t0002g0116 a0001c0001t0004g0002 a0001c0001t0004g0006 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+11251G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541741 | |||||||
| chr11:47541744 | A | C | 4 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0008 others(1): Show |
5 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-154+11248T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541744 | |||||||
| chr11:47541748 | A | C | 3 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0006 |
3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11244T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541748 | |||||||
| chr11:47541752 | A | C | 2 | a0001c0001t0004g0005 a0001c0001t0004g0007 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11240T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541752 | |||||||
| chr11:47541752 | AAGAACGA others(51): Show |
A | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+11182_-154+11 others(64): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541752 | |||||||
| chr11:47541753 | AGAACGAA others(21): Show |
A | 2 | a0001c0001t0004g0008 a0001c0001t0004g0009 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-154+11211_-154+11 others(34): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541753 | |||||||
| chr11:47541756 | A | C | 2 | a0001c0001t0004g0001 a0001c0001t0004g0002 |
3 | HG01884.hp1 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-154+11236T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541756 | |||||||
| chr11:47541757 | C | A | 10 | a0001c0001t0004g0001 a0001c0001t0004g0002 a0001c0001t0004g0003 others(7): Show |
11 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-154+11235G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541757 | |||||||
| chr11:47541760 | A | C | 3 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0006 |
3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11232T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541760 | |||||||
| chr11:47541764 | A | C | 2 | a0001c0001t0004g0005 a0001c0001t0004g0007 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11228T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541764 | |||||||
| chr11:47541767 | A | G | 1 | a0001c0001t0007g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+11225T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541767 | |||||||
| chr11:47541768 | A | C | 2 | a0001c0001t0004g0001 a0001c0001t0004g0002 |
3 | HG01884.hp1 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-154+11224T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541768 | |||||||
| chr11:47541769 | C | A | 11 | a0001c0001t0001g0198 a0001c0001t0004g0001 a0001c0001t0004g0002 others(8): Show |
12 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-154+11223G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541769 | |||||||
| chr11:47541772 | A | C | 3 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0006 |
3 | HG03225.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11220T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541772 | |||||||
| chr11:47541776 | A | C | 2 | a0001c0001t0004g0005 a0001c0001t0004g0007 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-154+11216T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541776 | |||||||
| chr11:47541780 | A | C | 1 | a0001c0001t0004g0001 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-154+11212T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541780 | |||||||
| chr11:47541781 | C | A | 14 | a0001c0001t0001g0133 a0001c0001t0001g0163 a0001c0001t0001g0180 others(11): Show |
15 | HG01884.hp1 HG01978.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-154+11211G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541781 | |||||||
| chr11:47541781 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11211G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541781 | |||||||
| chr11:47541782 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+11210C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541782 | |||||||
| chr11:47541784 | A | C | 3 | a0001c0001t0004g0003 a0001c0001t0004g0004 a0001c0001t0004g0009 |
3 | HG02055.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+11208T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541784 | |||||||
| chr11:47541786 | G | A | 4 | a0001c0001t0002g0108 a0001c0001t0002g0227 a0001c0001t0003g0058 others(1): Show |
4 | HG01975.hp2 HG02293.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11206C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541786 | |||||||
| chr11:47541788 | A | C | 1 | a0001c0001t0004g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-154+11204T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541788 | |||||||
| chr11:47541790 | G | A | 3 | a0001c0001t0002g0108 a0001c0001t0002g0227 a0001c0001t0021g0082 |
3 | HG02293.hp2 HG02451.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-154+11202C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541790 | |||||||
| chr11:47541791 | A | AAAGAAAG others(531): Show |
1 | a0001c0001t0007g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+11200_-154+11 others(544): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541791 | |||||||
| chr11:47541793 | C | A | 97 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0019 others(94): Show |
98 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(95): Show |
intron_variant | MODIFIER | c.-154+11199G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541793 | |||||||
| chr11:47541798 | G | A | 93 | a0001c0001t0001g0319 a0001c0001t0002g0024 a0001c0001t0002g0025 others(90): Show |
93 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-154+11194C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541798 | |||||||
| chr11:47541802 | G | A | 80 | a0001c0001t0001g0319 a0001c0001t0002g0024 a0001c0001t0002g0025 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+11190C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541802 | |||||||
| chr11:47541806 | G | A | 24 | a0001c0001t0001g0319 a0001c0001t0002g0273 a0001c0001t0002g0274 others(21): Show |
24 | HG00544.hp2 HG00621.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+11186C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541806 | |||||||
| chr11:47541810 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11182C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541810 | |||||||
| chr11:47541811 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+11181T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541811 | |||||||
| chr11:47541821 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+11171T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541821 | |||||||
| chr11:47541868 | G | A | 1 | a0001c0004t0002g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-154+11124C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47541868 | |||||||
| chr11:47542053 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+10939T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542053 | |||||||
| chr11:47542098 | G | A | 2 | a0001c0001t0008g0089 a0001c0001t0008g0099 |
2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-154+10894C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542098 | |||||||
| chr11:47542172 | C | G | 1 | a0001c0001t0002g0277 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-154+10820G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542172 | |||||||
| chr11:47542188 | G | C | 2 | a0001c0001t0001g0334 a0001c0001t0013g0333 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-154+10804C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542188 | |||||||
| chr11:47542381 | C | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+10611G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542381 | |||||||
| chr11:47542383 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+10609C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542383 | |||||||
| chr11:47542433 | G | T | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+10559C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542433 | |||||||
| chr11:47542496 | A | AT | 21 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0161 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-154+10495dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542496 | |||||||
| chr11:47542496 | AT | A | 24 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0159 others(21): Show |
24 | HG00609.hp1 HG02109.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+10495delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542496 | |||||||
| chr11:47542506 | T | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+10486A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542506 | |||||||
| chr11:47542667 | C | A | 1 | a0001c0001t0014g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-154+10325G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542667 | |||||||
| chr11:47542740 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-154+10252G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542740 | |||||||
| chr11:47542742 | CGT | C | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+10248_-154+10 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542742 | |||||||
| chr11:47542787 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-154+10205G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542787 | |||||||
| chr11:47542889 | T | C | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+10103A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47542889 | |||||||
| chr11:47543035 | G | A | 102 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
102 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-154+9957C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543035 | |||||||
| chr11:47543036 | C | T | 1 | a0001c0001t0002g0230 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-154+9956G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543036 | |||||||
| chr11:47543166 | G | C | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+9826C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543166 | |||||||
| chr11:47543170 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0118 a0001c0001t0001g0127 others(10): Show |
13 | HG00280.hp1 HG00741.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+9822C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543170 | |||||||
| chr11:47543182 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-154+9810A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543182 | |||||||
| chr11:47543197 | G | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0162 |
3 | HG02622.hp2 HG02717.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-154+9795C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543197 | |||||||
| chr11:47543233 | A | G | 59 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+9759T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543233 | |||||||
| chr11:47543404 | G | A | 22 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-154+9588C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543404 | |||||||
| chr11:47543551 | G | T | 28 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-154+9441C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543551 | |||||||
| chr11:47543586 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 |
3 | HG01175.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+9406A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543586 | |||||||
| chr11:47543639 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+9353C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543639 | |||||||
| chr11:47543663 | A | C | 1 | a0001c0001t0001g0330 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-154+9329T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543663 | |||||||
| chr11:47543726 | A | G | 1 | a0001c0001t0003g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-154+9266T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543726 | |||||||
| chr11:47543761 | TA | T | 106 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(103): Show |
106 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.-154+9230delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543761 | |||||||
| chr11:47543784 | C | T | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+9208G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47543784 | |||||||
| chr11:47544358 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+8634C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544358 | |||||||
| chr11:47544613 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-154+8379T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544613 | |||||||
| chr11:47544680 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-154+8312C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544680 | |||||||
| chr11:47544703 | T | G | 1 | a0001c0001t0003g0063 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-154+8289A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544703 | |||||||
| chr11:47544800 | T | C | 102 | a0001c0001t0001g0098 a0001c0001t0002g0028 a0001c0001t0002g0029 others(99): Show |
103 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-154+8192A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544800 | |||||||
| chr11:47544859 | G | A | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+8133C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544859 | |||||||
| chr11:47544946 | C | G | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+8046G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47544946 | |||||||
| chr11:47545109 | A | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+7883T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545109 | |||||||
| chr11:47545195 | C | G | 1 | a0001c0001t0006g0113 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-154+7797G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545195 | |||||||
| chr11:47545196 | G | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0121 others(26): Show |
29 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.-154+7796C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545196 | |||||||
| chr11:47545337 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-154+7655G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545337 | |||||||
| chr11:47545431 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-154+7561T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545431 | |||||||
| chr11:47545502 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7490T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545502 | |||||||
| chr11:47545604 | C | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0193 a0001c0001t0001g0195 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+7388G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545604 | |||||||
| chr11:47545643 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-154+7349T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545643 | |||||||
| chr11:47545700 | T | C | 20 | a0001c0001t0003g0035 a0001c0001t0003g0040 a0001c0001t0003g0041 others(17): Show |
20 | HG00558.hp1 HG00673.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-154+7292A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545700 | |||||||
| chr11:47545799 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-154+7193C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545799 | |||||||
| chr11:47545850 | C | CGT | 4 | a0001c0001t0002g0110 a0001c0001t0002g0112 a0001c0001t0002g0248 others(1): Show |
4 | HG01167.hp1 HG01169.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7140_-154+714 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | |||||||
| chr11:47545850 | C | T | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+7142G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | |||||||
| chr11:47545850 | CGTGTGTG others(15): Show |
C | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+7120_-154+714 others(26): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | |||||||
| chr11:47545850 | CGTGTGTG others(21): Show |
C | 19 | a0001c0001t0003g0035 a0001c0001t0003g0040 a0001c0001t0003g0041 others(16): Show |
19 | HG00558.hp1 HG00673.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+7114_-154+714 others(32): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545850 | |||||||
| chr11:47545852 | TGTGTGTG others(11): Show |
T | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-154+7122_-154+713 others(22): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545852 | |||||||
| chr11:47545858 | TGTGTGTG others(5): Show |
T | 1 | a0001c0001t0001g0319 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-154+7122_-154+713 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545858 | |||||||
| chr11:47545862 | TGTGTCTG others(1): Show |
T | 4 | a0001c0001t0001g0187 a0001c0001t0002g0108 a0001c0002t0002g0299 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545862 | |||||||
| chr11:47545865 | GTC | G | 4 | a0001c0001t0002g0231 a0001c0001t0002g0250 a0001c0001t0002g0282 others(1): Show |
4 | HG01346.hp1 HG01433.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+7125_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545865 | |||||||
| chr11:47545866 | TCTGC | T | 3 | a0001c0001t0002g0272 a0001c0001t0004g0003 a0001c0001t0004g0004 |
3 | HG03017.hp2 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545866 | |||||||
| chr11:47545867 | C | CTG | 22 | a0001c0001t0002g0024 a0001c0001t0002g0107 a0001c0001t0002g0109 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-154+7123_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | C | CTGTG | 33 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 others(30): Show |
33 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | C | CTGTGTG | 6 | a0001c0001t0002g0223 a0001c0001t0002g0229 a0001c0001t0002g0244 others(3): Show |
6 | HG02071.hp1 HG02683.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | C | CTGTGTGT others(1): Show |
5 | a0001c0001t0002g0274 a0001c0001t0002g0275 a0001c0001t0002g0289 others(2): Show |
5 | HG01517.hp2 HG03239.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+7124_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0002g0252 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-154+7124_-154+712 others(24): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | C | G | 7 | a0001c0001t0002g0248 a0001c0001t0004g0001 a0001c0001t0004g0005 others(4): Show |
8 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7125G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | CTGCG | C | 122 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(119): Show |
122 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-154+7121_-154+712 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | CTGCGTG | C | 14 | a0001c0001t0001g0026 a0001c0001t0001g0128 a0001c0001t0001g0170 others(11): Show |
14 | HG01081.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.-154+7119_-154+712 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | CTGCGTGT others(1): Show |
C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0192 a0001c0001t0003g0037 |
3 | HG00609.hp1 HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-154+7117_-154+712 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545867 | CTGCGTGT others(7): Show |
C | 1 | a0001c0001t0002g0302 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-154+7111_-154+712 others(18): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545867 | |||||||
| chr11:47545868 | TGC | T | 11 | a0001c0001t0001g0190 a0001c0001t0001g0331 a0001c0001t0002g0247 others(8): Show |
11 | HG01361.hp1 HG01975.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.-154+7122_-154+712 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545868 | |||||||
| chr11:47545870 | C | T | 151 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0120 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.-154+7122G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545870 | |||||||
| chr11:47545871 | G | C | 5 | a0001c0001t0004g0001 a0001c0001t0004g0005 a0001c0001t0004g0006 others(2): Show |
6 | HG01884.hp1 HG02559.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+7121C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545871 | |||||||
| chr11:47545873 | G | C | 1 | a0001c0001t0004g0002 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-154+7119C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545873 | |||||||
| chr11:47545875 | G | C | 2 | a0001c0001t0004g0003 a0001c0001t0004g0004 |
2 | HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-154+7117C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545875 | |||||||
| chr11:47545901 | G | A | 1 | a0001c0001t0003g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-154+7091C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545901 | |||||||
| chr11:47545903 | G | A | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0162 others(5): Show |
8 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7089C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545903 | |||||||
| chr11:47545905 | G | A | 132 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0098 others(129): Show |
133 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-154+7087C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545905 | |||||||
| chr11:47545905 | G | GTA | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0305 others(1): Show |
4 | HG01099.hp2 HG01257.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-154+7085_-154+708 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545905 | |||||||
| chr11:47545907 | A | G | 26 | a0001c0001t0002g0013 a0001c0001t0002g0106 a0001c0001t0002g0107 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.-154+7085T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545907 | |||||||
| chr11:47545909 | A | G | 2 | a0001c0001t0002g0116 a0001c0001t0006g0104 |
2 | HG01081.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-154+7083T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545909 | |||||||
| chr11:47545915 | A | T | 12 | a0001c0001t0001g0338 a0001c0001t0002g0226 a0001c0001t0002g0227 others(9): Show |
12 | HG01358.hp2 HG03471.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+7077T>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | |||||||
| chr11:47545915 | AT | A | 80 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
80 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.-154+7076delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | |||||||
| chr11:47545915 | ATT | A | 6 | a0001c0001t0001g0026 a0001c0001t0002g0011 a0001c0001t0002g0012 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+7075_-154+707 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | |||||||
| chr11:47545915 | ATTT | A | 24 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0120 others(21): Show |
24 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.-154+7074_-154+707 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545915 | |||||||
| chr11:47545917 | T | A | 112 | a0001c0001t0001g0098 a0001c0001t0001g0322 a0001c0001t0001g0324 others(109): Show |
112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-154+7075A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545917 | |||||||
| chr11:47545918 | T | A | 79 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.-154+7074A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545918 | |||||||
| chr11:47545919 | T | A | 8 | a0001c0001t0001g0026 a0001c0001t0002g0076 a0001c0001t0003g0075 others(5): Show |
8 | HG00323.hp1 HG00642.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+7073A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545919 | |||||||
| chr11:47545921 | T | A | 1 | a0001c0001t0024g0320 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-154+7071A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47545921 | |||||||
| chr11:47546003 | C | G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0297 a0001c0001t0003g0298 |
3 | HG00597.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-154+6989G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546003 | |||||||
| chr11:47546012 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0030 |
2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-154+6980C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546012 | |||||||
| chr11:47546236 | C | CTT | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+6754_-154+675 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546236 | |||||||
| chr11:47546236 | CT | C | 300 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(297): Show |
301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-154+6755delA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546236 | |||||||
| chr11:47546253 | T | G | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6739A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546253 | |||||||
| chr11:47546256 | G | C | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6736C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546256 | |||||||
| chr11:47546257 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-154+6735G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546257 | |||||||
| chr11:47546270 | C | CG | 29 | a0001c0001t0001g0018 a0001c0001t0001g0133 a0001c0001t0001g0137 others(26): Show |
29 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-154+6721dupC | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | |||||||
| chr11:47546270 | C | G | 1 | a0001c0001t0004g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-154+6722G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | |||||||
| chr11:47546270 | C | T | 1 | a0001c0001t0007g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+6722G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546270 | |||||||
| chr11:47546276 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-154+6716G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546276 | |||||||
| chr11:47546277 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-154+6715C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546277 | |||||||
| chr11:47546322 | A | G | 1 | a0001c0001t0002g0226 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-154+6670T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546322 | |||||||
| chr11:47546425 | C | G | 1 | a0001c0001t0027g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-154+6567G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546425 | |||||||
| chr11:47546522 | C | T | 77 | a0001c0001t0001g0098 a0001c0001t0002g0076 a0001c0001t0003g0014 others(74): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-154+6470G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546522 | |||||||
| chr11:47546525 | C | T | 1 | a0001c0001t0004g0002 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-154+6467G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546525 | |||||||
| chr11:47546699 | T | C | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+6293A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546699 | |||||||
| chr11:47546750 | T | C | 4 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0253 others(1): Show |
4 | HG01167.hp2 HG01258.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+6242A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546750 | |||||||
| chr11:47546792 | C | G | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+6200G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546792 | |||||||
| chr11:47546892 | T | C | 333 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(330): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-154+6100A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47546892 | |||||||
| chr11:47547049 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+5943T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547049 | |||||||
| chr11:47547057 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-154+5935G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547057 | |||||||
| chr11:47547065 | C | A | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+5927G>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CA | 6 | a0001c0001t0001g0339 a0001c0001t0002g0108 a0001c0001t0010g0101 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+5926dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAA | 7 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0002g0224 others(4): Show |
7 | HG02165.hp1 HG02258.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+5925_-154+592 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAA | 61 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0002g0011 others(58): Show |
62 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-154+5924_-154+592 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAA | 38 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(35): Show |
38 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.-154+5923_-154+592 others(8): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAA | 27 | a0001c0001t0001g0010 a0001c0001t0001g0135 a0001c0001t0001g0136 others(24): Show |
27 | HG00621.hp2 HG00642.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-154+5922_-154+592 others(9): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAA | 32 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0027 others(29): Show |
32 | HG00544.hp1 HG01175.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.-154+5921_-154+592 others(10): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA | 22 | a0001c0001t0001g0026 a0001c0001t0001g0126 a0001c0001t0001g0158 others(19): Show |
22 | HG00558.hp2 HG00609.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-154+5920_-154+592 others(11): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA others(1): Show |
19 | a0001c0001t0001g0022 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG00280.hp1 HG00408.hp1 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+5919_-154+592 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0184 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.-154+5918_-154+592 others(13): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0187 a0001c0001t0001g0201 a0001c0001t0001g0206 others(2): Show |
5 | HG02258.hp2 HG02698.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+5917_-154+592 others(14): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0202 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-154+5916_-154+592 others(15): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-154+5915_-154+592 others(16): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | CAA | C | 13 | a0001c0001t0003g0023 a0001c0001t0003g0035 a0001c0001t0003g0080 others(10): Show |
13 | HG01175.hp2 HG01361.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+5925_-154+592 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | CAAA | C | 63 | a0001c0001t0002g0076 a0001c0001t0003g0014 a0001c0001t0003g0015 others(60): Show |
63 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-154+5924_-154+592 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01081.hp2 HG01099.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+5919_-154+592 others(12): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547065 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0002g0105 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02965.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-154+5914_-154+592 others(17): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547065 | |||||||
| chr11:47547088 | A | G | 1 | a0001c0001t0007g0211 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-154+5904T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547088 | |||||||
| chr11:47547174 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+5818C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547174 | |||||||
| chr11:47547307 | T | C | 3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0263 |
3 | NA18990.hp2 NA18995.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-154+5685A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547307 | |||||||
| chr11:47547394 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-154+5598T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547394 | |||||||
| chr11:47547508 | T | A | 1 | a0001c0001t0002g0264 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-154+5484A>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547508 | |||||||
| chr11:47547624 | G | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+5368C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547624 | |||||||
| chr11:47547681 | AAAG | A | 91 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(88): Show |
91 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-154+5308_-154+531 others(7): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547681 | |||||||
| chr11:47547682 | AAG | A | 15 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0230 others(12): Show |
15 | HG00408.hp2 HG01261.hp1 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-154+5308_-154+530 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547682 | |||||||
| chr11:47547846 | G | C | 1 | a0001c0001t0002g0265 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-154+5146C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547846 | |||||||
| chr11:47547849 | T | C | 10 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(7): Show |
10 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-154+5143A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47547849 | |||||||
| chr11:47548054 | A | G | 3 | a0001c0001t0007g0016 a0001c0001t0007g0119 a0001c0001t0007g0211 |
3 | HG02109.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-154+4938T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548054 | |||||||
| chr11:47548192 | G | A | 2 | a0001c0003t0011g0308 a0001c0003t0011g0309 |
2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-154+4800C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548192 | |||||||
| chr11:47548227 | C | T | 13 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(10): Show |
13 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-154+4765G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548227 | |||||||
| chr11:47548403 | C | G | 2 | a0001c0001t0003g0035 a0001c0001t0028g0034 |
2 | HG00735.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-154+4589G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548403 | |||||||
| chr11:47548518 | T | G | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+4474A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548518 | |||||||
| chr11:47548865 | C | CA | 124 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0098 others(121): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-154+4126dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | |||||||
| chr11:47548865 | C | CAA | 13 | a0001c0001t0002g0012 a0001c0001t0002g0116 a0001c0001t0002g0266 others(10): Show |
13 | HG00438.hp1 HG00735.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-154+4125_-154+412 others(6): Show |
CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | |||||||
| chr11:47548865 | CA | C | 18 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(15): Show |
18 | HG02109.hp2 HG02572.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-154+4126delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47548865 | |||||||
| chr11:47549059 | T | G | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02109.hp1 HG02698.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3933A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549059 | |||||||
| chr11:47549171 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3821C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549171 | |||||||
| chr11:47549479 | A | G | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+3513T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549479 | |||||||
| chr11:47549809 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+3183C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549809 | |||||||
| chr11:47549812 | T | G | 1 | a0001c0001t0002g0116 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-154+3180A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549812 | |||||||
| chr11:47549816 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-154+3176A>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549816 | |||||||
| chr11:47549820 | G | GT | 85 | a0001c0001t0001g0098 a0001c0001t0001g0171 a0001c0001t0001g0175 others(82): Show |
85 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-154+3171dupA | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549820 | |||||||
| chr11:47549820 | G | T | 1 | a0001c0001t0003g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-154+3172C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549820 | |||||||
| chr11:47549848 | G | A | 2 | a0001c0001t0010g0101 a0001c0001t0010g0102 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-154+3144C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549848 | |||||||
| chr11:47549905 | C | T | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 |
3 | HG00741.hp1 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-154+3087G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47549905 | |||||||
| chr11:47550064 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-154+2928G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550064 | |||||||
| chr11:47550082 | T | C | 1 | a0001c0001t0006g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-154+2910A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550082 | |||||||
| chr11:47550216 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-154+2776G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550216 | |||||||
| chr11:47550239 | C | CA | 14 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0319 others(11): Show |
14 | HG01071.hp2 HG01175.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+2752dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550239 | |||||||
| chr11:47550243 | A | C | 1 | a0001c0001t0006g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-154+2749T>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550243 | |||||||
| chr11:47550256 | T | C | 108 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 others(105): Show |
108 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-154+2736A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550256 | |||||||
| chr11:47550291 | G | C | 1 | a0001c0001t0026g0291 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-154+2701C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550291 | |||||||
| chr11:47550303 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
107 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-154+2689C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550303 | |||||||
| chr11:47550340 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2652C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550340 | |||||||
| chr11:47550369 | A | G | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG01071.hp2 HG01099.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+2623T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550369 | |||||||
| chr11:47550404 | G | A | 107 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
107 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-154+2588C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550404 | |||||||
| chr11:47550415 | C | T | 59 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.-154+2577G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550415 | |||||||
| chr11:47550460 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2532C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550460 | |||||||
| chr11:47550639 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-154+2353A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550639 | |||||||
| chr11:47550727 | G | A | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+2265C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550727 | |||||||
| chr11:47550742 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+2250C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47550742 | |||||||
| chr11:47551039 | TA | T | 318 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(315): Show |
319 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.-154+1952delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551039 | |||||||
| chr11:47551342 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-154+1650G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551342 | |||||||
| chr11:47551404 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+1588C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551404 | |||||||
| chr11:47551497 | T | C | 1 | a0001c0001t0003g0216 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-154+1495A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551497 | |||||||
| chr11:47551541 | T | C | 1 | a0001c0001t0002g0296 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-154+1451A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551541 | |||||||
| chr11:47551542 | G | A | 5 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+1450C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551542 | |||||||
| chr11:47551574 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+1418G>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551574 | |||||||
| chr11:47551790 | G | A | 80 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0222 others(77): Show |
80 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-154+1202C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47551790 | |||||||
| chr11:47552013 | T | TA | 7 | a0001c0001t0001g0301 a0001c0001t0002g0302 a0001c0001t0003g0297 others(4): Show |
7 | HG00597.hp1 HG00609.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+978dupT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552013 | |||||||
| chr11:47552013 | TA | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(11): Show |
14 | HG00558.hp2 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-154+978delT | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552013 | |||||||
| chr11:47552056 | T | C | 1 | a0001c0001t0002g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-154+936A>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552056 | |||||||
| chr11:47552378 | G | C | 3 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0307 |
3 | HG01071.hp2 HG01257.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-154+614C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552378 | |||||||
| chr11:47552380 | G | C | 4 | a0001c0001t0001g0319 a0001c0001t0024g0320 a0001c0003t0011g0308 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+612C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552380 | |||||||
| chr11:47552529 | C | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0013 |
3 | HG01175.hp1 HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+463G>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552529 | |||||||
| chr11:47552658 | G | C | 1 | a0001c0001t0002g0318 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-154+334C>G | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552658 | |||||||
| chr11:47552726 | G | A | 9 | a0001c0001t0002g0310 a0001c0001t0002g0311 a0001c0001t0002g0312 others(6): Show |
9 | HG00280.hp2 HG01255.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+266C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552726 | |||||||
| chr11:47552777 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0024g0320 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-154+215C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552777 | |||||||
| chr11:47552823 | G | A | 1 | a0001c0001t0003g0321 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-154+169C>T | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552823 | |||||||
| chr11:47552864 | A | G | 320 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(317): Show |
321 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.-154+128T>C | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552864 | |||||||
| chr11:47552908 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-154+84C>A | CELF1 | ENSG00000149187.19 | transcript | ENST00000687097.1 | protein_coding | 1/14 | chr11 | 47552908 |