Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 92906 |
| ensemblid | ENSG00000143889.16 |
| hgncid | 25127 |
| symbol | HNRNPLL |
| name | heterogeneous nuclear ribonucleoprotein L like |
| refseq_nuc | NM_138394.4 |
| refseq_prot | NP_612403.2 |
| ensembl_nuc | ENST00000449105.8 |
| ensembl_prot | ENSP00000390625.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 38561969 |
| end | 38602928 |
| strand | - |
| ver | v1.2 |
| region | chr2:38561969-38602928 |
| region5000 | chr2:38556969-38607928 |
| regionname0 | HNRNPLL_chr2_38561969_38602928 |
| regionname5000 | HNRNPLL_chr2_38556969_38607928 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 542 | 316 | 87 | 60 | 121 | 12 | 34 | 87 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | MSSSS others(537): Show |
chr2 | 38556969 | 38607928 |
| a0002 | 0/0 | 543 | 11 | 3 | 0 | 8 | 0 | 0 | 8 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | MSSSS others(538): Show |
chr2 | 38556969 | 38607928 |
| a0003 | 0/0 | 542 | 9 | 0 | 0 | 9 | 0 | 0 | 9 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | MSSSS others(537): Show |
chr2 | 38556969 | 38607928 |
| a0004 | 0/0 | 542 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | MSSSS others(537): Show |
chr2 | 38556969 | 38607928 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1626 | 315 | 87 | 59 | 121 | 12 | 34 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATGTC others(1621): Show |
chr2 | 38556969 | 38607928 | ||
| a0001c0005 | 0/0 | 1626 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATGTC others(1621): Show |
chr2 | 38556969 | 38607928 | ||
| a0002c0002 | 0/0 | 1629 | 11 | 3 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATGTC others(1624): Show |
chr2 | 38556969 | 38607928 | ||
| a0003c0003 | 0/0 | 1626 | 9 | 0 | 0 | 9 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATGTC others(1621): Show |
chr2 | 38556969 | 38607928 | ||
| a0004c0004 | 0/0 | 1626 | 2 | 0 | 0 | 0 | 2 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATGTC others(1621): Show |
chr2 | 38556969 | 38607928 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4144 | 164 | 26 | 38 | 67 | 6 | 25 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0002 | 0/0 | 4144 | 57 | 25 | 8 | 24 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0003 | 0/0 | 4144 | 30 | 9 | 1 | 15 | 3 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0004 | 0/0 | 4144 | 11 | 1 | 2 | 4 | 1 | 3 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0005 | 0/0 | 4144 | 10 | 1 | 7 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0007 | 0/0 | 4144 | 6 | 6 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0008 | 0/0 | 4144 | 5 | 0 | 0 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0009 | 0/0 | 4144 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0010 | 0/0 | 4144 | 5 | 4 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0011 | 0/0 | 4144 | 4 | 3 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0012 | 0/0 | 4144 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0014 | 0/0 | 4144 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0015 | 0/0 | 4144 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0016 | 0/0 | 4144 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0017 | 0/0 | 4144 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0018 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0019 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0020 | 0/0 | 4144 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0021 | 0/0 | 4144 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0022 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0023 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0001t0024 | 0/0 | 4144 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0001c0005t0001 | 0/0 | 4144 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0002c0002t0006 | 0/0 | 4147 | 8 | 0 | 0 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4142): Show |
chr2 | 38556969 | 38607928 |
| a0002c0002t0013 | 0/0 | 4147 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4142): Show |
chr2 | 38556969 | 38607928 |
| a0003c0003t0004 | 0/0 | 4144 | 9 | 0 | 0 | 9 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| a0004c0004t0001 | 0/0 | 4144 | 2 | 0 | 0 | 0 | 2 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | ATCCT others(4139): Show |
chr2 | 38556969 | 38607928 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 3 | 10 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0008 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0009g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0010g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0011g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0011g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0012g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0016g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0016g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0018g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0019g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0020g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0021g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0001t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0001c0005t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0013g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0002c0002t0013g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0003c0003t0004g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0003c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0003c0003t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0003c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0004c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| a0004c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0033 | EUR | GBR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01192 | hp1 | a0001 | c0005 | t0001 | g0144 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01258 | hp2 | a0001 | c0001 | t0015 | g0197 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0219 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01496 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01515 | hp1 | a0004 | c0004 | t0001 | g0257 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0116 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01884 | hp2 | a0001 | c0001 | t0023 | g0047 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02155 | hp1 | a0001 | c0001 | t0020 | g0076 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0042 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0102 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0229 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0109 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0030 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02818 | hp2 | a0001 | c0001 | t0022 | g0037 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0101 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0234 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03139 | hp2 | a0001 | c0001 | t0024 | g0066 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03540 | hp2 | a0001 | c0001 | t0018 | g0108 | AFR | GWD | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03669 | hp2 | a0001 | c0001 | t0017 | g0191 | SAS | PJL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0111 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG04204 | hp2 | a0001 | c0001 | t0014 | g0094 | SAS | STU | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0218 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18906 | hp1 | a0002 | c0002 | t0013 | g0035 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18945 | hp2 | a0002 | c0002 | t0006 | g0251 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18950 | hp1 | a0002 | c0002 | t0006 | g0256 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18951 | hp1 | a0001 | c0001 | t0012 | g0133 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18951 | hp2 | a0002 | c0002 | t0006 | g0249 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18957 | hp2 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18960 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18974 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18980 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18980 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18983 | hp1 | a0001 | c0001 | t0012 | g0148 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18988 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18994 | hp2 | a0002 | c0002 | t0006 | g0254 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18999 | hp2 | a0001 | c0001 | t0021 | g0238 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19003 | hp2 | a0002 | c0002 | t0006 | g0252 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19030 | hp2 | a0002 | c0002 | t0013 | g0248 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19043 | hp2 | a0002 | c0002 | t0013 | g0035 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19060 | hp1 | a0001 | c0001 | t0008 | g0213 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19060 | hp2 | a0003 | c0003 | t0004 | g0244 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19062 | hp1 | a0003 | c0003 | t0004 | g0241 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19063 | hp2 | a0002 | c0002 | t0006 | g0255 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19079 | hp1 | a0002 | c0002 | t0006 | g0250 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19084 | hp1 | a0002 | c0002 | t0006 | g0253 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19087 | hp1 | a0003 | c0003 | t0004 | g0005 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19088 | hp2 | a0003 | c0003 | t0004 | g0245 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0237 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | YRI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ASW | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20752 | hp2 | a0004 | c0004 | t0001 | g0258 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0013 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20805 | hp2 | a0001 | c0001 | t0015 | g0184 | EUR | TSI | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | GIH | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | CLM | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA20300 | hp2 | a0001 | c0001 | t0019 | g0171 | AFR | USA | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0117 | REF | REF | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0146 | REF | REF | HNRNPLL_chr2_38556969_38607928 | HNRNPLL | chr2 | 38556969 | 38607928 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38561969 | T | G | 1 | a0002 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
splice_region_variant | LOW | c.*2213A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | chr2 | 38561969 | |||||||
| chr2:38582079 | T | C | 1 | a0003 | 9 | NA18957.hp2 NA18960.hp1 NA18974.hp1 others(6): Show |
missense_variant | MODERATE | c.722A>G | p.Tyr241Cys | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/13 | 1024/4144 | 722/1629 | 241/542 | chr2 | 38582079 | |||
| chr2:38602455 | G | GGCC | 1 | a0002 | 11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
conservative_inframe_insertion | MODERATE | c.169_171dupGGC | p.Gly57dup | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/13 | 473/4144 | 171/1629 | 57/542 | chr2 | 38602455 | |||
| chr2:38602595 | G | A | 1 | a0004 | 2 | HG01515.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.32C>T | p.Thr11Met | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/13 | 334/4144 | 32/1629 | 11/542 | chr2 | 38602595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38569136 | T | C | 1 | a0001c0005 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1413A>G | p.Thr471Thr | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/13 | 1715/4144 | 1413/1629 | 471/542 | chr2 | 38569136 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38561994 | A | G | 1 | a0001c0001t0016 | 2 | HG02630.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2188 | chr2 | 38561994 | ||||||
| chr2:38562039 | A | G | 1 | a0001c0001t0005 | 10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2143T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2143 | chr2 | 38562039 | ||||||
| chr2:38562043 | T | A | 1 | a0001c0001t0015 | 2 | HG01258.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2139A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2139 | chr2 | 38562043 | ||||||
| chr2:38562049 | T | A | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0020 others(2): Show |
47 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2133A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2133 | chr2 | 38562049 | ||||||
| chr2:38562101 | T | C | 3 | a0001c0001t0004 a0001c0001t0021 a0003c0003t0004 |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2081A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2081 | chr2 | 38562101 | ||||||
| chr2:38562103 | G | T | 1 | a0001c0001t0021 | 1 | NA18999.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2079C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2079 | chr2 | 38562103 | ||||||
| chr2:38562163 | G | C | 1 | a0001c0001t0020 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2019C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 2019 | chr2 | 38562163 | ||||||
| chr2:38562351 | T | C | 1 | a0001c0001t0007 | 6 | HG02280.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1831A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1831 | chr2 | 38562351 | ||||||
| chr2:38562366 | T | A | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
152 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1816A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1816 | chr2 | 38562366 | ||||||
| chr2:38562383 | A | G | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0021 others(2): Show |
33 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1799T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1799 | chr2 | 38562383 | ||||||
| chr2:38562540 | A | G | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0020 |
36 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1642T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1642 | chr2 | 38562540 | ||||||
| chr2:38562545 | T | G | 1 | a0002c0002t0006 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1637A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1637 | chr2 | 38562545 | ||||||
| chr2:38562643 | C | A | 1 | a0001c0001t0022 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1539G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1539 | chr2 | 38562643 | ||||||
| chr2:38562850 | C | T | 1 | a0001c0001t0014 | 2 | HG04184.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1332G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1332 | chr2 | 38562850 | ||||||
| chr2:38562976 | A | G | 2 | a0001c0001t0009 a0001c0001t0019 |
6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1206T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1206 | chr2 | 38562976 | ||||||
| chr2:38562980 | C | T | 1 | a0002c0002t0006 | 8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1202G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1202 | chr2 | 38562980 | ||||||
| chr2:38563161 | C | T | 1 | a0001c0001t0018 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1021G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 1021 | chr2 | 38563161 | ||||||
| chr2:38563269 | C | T | 1 | a0001c0001t0017 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 913 | chr2 | 38563269 | ||||||
| chr2:38563308 | A | T | 1 | a0001c0001t0008 | 5 | NA18941.hp2 NA18956.hp1 NA19003.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*874T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 874 | chr2 | 38563308 | ||||||
| chr2:38563373 | T | G | 1 | a0001c0001t0012 | 4 | HG02129.hp2 NA18951.hp1 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*809A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 809 | chr2 | 38563373 | ||||||
| chr2:38563630 | G | A | 1 | a0001c0001t0010 | 5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 552 | chr2 | 38563630 | ||||||
| chr2:38563758 | G | A | 1 | a0001c0001t0023 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 424 | chr2 | 38563758 | ||||||
| chr2:38563969 | T | C | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 13/13 | 213 | chr2 | 38563969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38564304 | G | C | 15 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(12): Show |
22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1574-67C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564304 | |||||||
| chr2:38564391 | C | T | 1 | a0001c0001t0007g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1574-154G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564391 | |||||||
| chr2:38564401 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-164G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564401 | |||||||
| chr2:38564451 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1574-214G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564451 | |||||||
| chr2:38564613 | C | CA | 33 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0122 others(30): Show |
37 | HG00140.hp1 HG00423.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1574-377dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | |||||||
| chr2:38564613 | C | CAA | 9 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0025 others(6): Show |
19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1574-378_1574-377d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | |||||||
| chr2:38564613 | C | CAAA | 6 | a0001c0001t0003g0007 a0001c0001t0003g0077 a0001c0001t0003g0079 others(3): Show |
9 | HG00597.hp1 HG02074.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.1574-379_1574-377d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | |||||||
| chr2:38564613 | C | CAAAA | 8 | a0001c0001t0003g0160 a0002c0002t0006g0249 a0002c0002t0006g0250 others(5): Show |
8 | HG06807.hp1 NA18945.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-380_1574-377d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564613 | |||||||
| chr2:38564700 | T | G | 14 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0038 others(11): Show |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1574-463A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564700 | |||||||
| chr2:38564725 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-488G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564725 | |||||||
| chr2:38564769 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1574-532A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564769 | |||||||
| chr2:38564778 | C | G | 84 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0002g0003 others(81): Show |
112 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1574-541G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564778 | |||||||
| chr2:38564835 | A | G | 1 | a0001c0001t0007g0164 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1574-598T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564835 | |||||||
| chr2:38564844 | A | G | 1 | a0001c0001t0007g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1574-607T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564844 | |||||||
| chr2:38564903 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1574-666A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38564903 | |||||||
| chr2:38565004 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-767T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565004 | |||||||
| chr2:38565008 | AC | A | 29 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(26): Show |
43 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1574-772delG | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565008 | |||||||
| chr2:38565009 | C | A | 52 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(49): Show |
65 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1574-772G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565009 | |||||||
| chr2:38565295 | A | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1574-1058T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565295 | |||||||
| chr2:38565578 | A | ATAAGCTG others(4): Show |
1 | a0001c0001t0004g0243 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1574-1352_1574-134 others(15): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565578 | |||||||
| chr2:38565594 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1574-1357C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565594 | |||||||
| chr2:38565609 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1574-1372G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565609 | |||||||
| chr2:38565647 | G | C | 1 | a0001c0001t0001g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1574-1410C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565647 | |||||||
| chr2:38565662 | G | A | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1574-1425C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565662 | |||||||
| chr2:38565678 | G | T | 1 | a0001c0001t0009g0153 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1574-1441C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565678 | |||||||
| chr2:38565727 | C | CA | 13 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0093 others(10): Show |
13 | HG01192.hp1 HG01255.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1574-1491dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CA | C | 41 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0104 others(38): Show |
51 | HG00673.hp2 HG00741.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1574-1491delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAA | C | 13 | a0001c0001t0001g0097 a0001c0001t0001g0140 a0001c0001t0001g0177 others(10): Show |
15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1574-1492_1574-149 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAA | C | 11 | a0001c0001t0002g0009 a0001c0001t0002g0082 a0001c0001t0002g0162 others(8): Show |
15 | HG01106.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1574-1493_1574-149 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAAA | C | 5 | a0001c0001t0003g0077 a0001c0001t0003g0085 a0001c0001t0004g0243 others(2): Show |
6 | HG03834.hp2 NA18906.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1574-1494_1574-149 others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAAAA | C | 38 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0007 others(35): Show |
58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1574-1495_1574-149 others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAAAAAA | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0135 a0001c0001t0001g0203 others(3): Show |
7 | HG00544.hp1 HG00639.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1574-1497_1574-149 others(11): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAAAAAA others(1): Show |
C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(46): Show |
67 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1574-1498_1574-149 others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565727 | CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0134 others(2): Show |
6 | HG00099.hp2 HG00735.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1574-1504_1574-149 others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565727 | |||||||
| chr2:38565786 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1574-1549A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565786 | |||||||
| chr2:38565856 | T | C | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1574-1619A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565856 | |||||||
| chr2:38565968 | G | GT | 25 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(22): Show |
39 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1574-1732dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38565968 | |||||||
| chr2:38566027 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1574-1790A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566027 | |||||||
| chr2:38566134 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1574-1897C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566134 | |||||||
| chr2:38566323 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+1876C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566323 | |||||||
| chr2:38566378 | A | AAC | 23 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(20): Show |
37 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1573+1820_1573+182 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566378 | |||||||
| chr2:38566378 | A | C | 3 | a0001c0001t0011g0029 a0001c0001t0011g0218 a0001c0001t0011g0219 |
4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+1821T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566378 | |||||||
| chr2:38566379 | C | A | 3 | a0001c0001t0003g0077 a0001c0001t0003g0088 a0001c0001t0003g0159 |
3 | HG02055.hp1 HG03471.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1573+1820G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566379 | |||||||
| chr2:38566379 | C | CA | 3 | a0001c0001t0011g0029 a0001c0001t0011g0218 a0001c0001t0011g0219 |
4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+1819_1573+182 others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566379 | |||||||
| chr2:38566380 | C | A | 27 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(24): Show |
42 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1573+1819G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | |||||||
| chr2:38566380 | C | CA | 29 | a0001c0001t0001g0090 a0001c0001t0001g0115 a0001c0001t0001g0128 others(26): Show |
35 | HG00738.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1573+1818dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | |||||||
| chr2:38566380 | C | CAA | 44 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0149 others(41): Show |
55 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1573+1817_1573+181 others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | |||||||
| chr2:38566380 | C | CAAA | 14 | a0001c0001t0002g0072 a0001c0001t0004g0033 a0001c0001t0004g0034 others(11): Show |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1573+1816_1573+181 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | |||||||
| chr2:38566380 | C | CCAA | 3 | a0001c0001t0003g0077 a0001c0001t0003g0088 a0001c0001t0003g0159 |
3 | HG02055.hp1 HG03471.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1573+1818_1573+181 others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566380 | |||||||
| chr2:38566408 | G | C | 2 | a0001c0001t0016g0101 a0001c0001t0016g0109 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1573+1791C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566408 | |||||||
| chr2:38566473 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+1726G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566473 | |||||||
| chr2:38566539 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573+1660T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566539 | |||||||
| chr2:38566582 | C | T | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+1617G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566582 | |||||||
| chr2:38566790 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1573+1409G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566790 | |||||||
| chr2:38566795 | G | C | 1 | a0001c0001t0022g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1573+1404C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566795 | |||||||
| chr2:38566796 | C | A | 1 | a0001c0001t0022g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1573+1403G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566796 | |||||||
| chr2:38566821 | T | TA | 9 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(6): Show |
11 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1573+1377dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566821 | |||||||
| chr2:38566844 | A | T | 1 | a0001c0001t0001g0189 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1573+1355T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566844 | |||||||
| chr2:38566870 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1573+1329C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38566870 | |||||||
| chr2:38567039 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1573+1160G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567039 | |||||||
| chr2:38567067 | A | T | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1573+1132T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567067 | |||||||
| chr2:38567126 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1573+1073G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567126 | |||||||
| chr2:38567165 | G | A | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1573+1034C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567165 | |||||||
| chr2:38567186 | C | T | 2 | a0001c0001t0016g0101 a0001c0001t0016g0109 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1573+1013G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567186 | |||||||
| chr2:38567224 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573+975A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567224 | |||||||
| chr2:38567225 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0235 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1573+974G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567225 | |||||||
| chr2:38567236 | G | C | 1 | a0001c0001t0002g0236 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1573+963C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567236 | |||||||
| chr2:38567245 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1573+954T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567245 | |||||||
| chr2:38567269 | A | AT | 22 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(19): Show |
36 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1573+929dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567269 | |||||||
| chr2:38567353 | C | T | 1 | a0002c0002t0006g0255 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1573+846G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567353 | |||||||
| chr2:38567430 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0141 |
3 | HG03942.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1573+769A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567430 | |||||||
| chr2:38567472 | G | C | 1 | a0001c0001t0005g0043 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1573+727C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567472 | |||||||
| chr2:38567481 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1573+718A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567481 | |||||||
| chr2:38567575 | G | A | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(15): Show |
31 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1573+624C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567575 | |||||||
| chr2:38567823 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1573+376T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567823 | |||||||
| chr2:38567937 | T | C | 2 | a0001c0001t0007g0098 a0001c0001t0018g0108 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1573+262A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38567937 | |||||||
| chr2:38568044 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1573+155T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38568044 | |||||||
| chr2:38568083 | T | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0162 a0001c0001t0002g0163 others(1): Show |
7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1573+116A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 12/12 | chr2 | 38568083 | |||||||
| chr2:38568374 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0212 |
3 | NA18979.hp1 NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1474+12G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 11/12 | chr2 | 38568374 | |||||||
| chr2:38568536 | T | C | 4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0235 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417-93A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568536 | |||||||
| chr2:38568614 | A | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0200 a0001c0001t0017g0191 |
3 | HG03492.hp2 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1417-171T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568614 | |||||||
| chr2:38568726 | G | A | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1417-283C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568726 | |||||||
| chr2:38568823 | G | C | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416+310C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568823 | |||||||
| chr2:38568860 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1416+273A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568860 | |||||||
| chr2:38568971 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1416+162T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38568971 | |||||||
| chr2:38569061 | A | C | 3 | a0001c0001t0002g0067 a0001c0001t0002g0070 a0001c0001t0002g0072 |
3 | HG03139.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1416+72T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38569061 | |||||||
| chr2:38569120 | T | C | 8 | a0001c0001t0007g0078 a0001c0001t0007g0098 a0001c0001t0007g0102 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416+13A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 10/12 | chr2 | 38569120 | |||||||
| chr2:38569423 | A | G | 1 | a0001c0001t0016g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1215-89T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569423 | |||||||
| chr2:38569483 | T | C | 1 | a0001c0001t0004g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1215-149A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569483 | |||||||
| chr2:38569542 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0162 a0001c0001t0002g0163 others(1): Show |
7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215-208A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569542 | |||||||
| chr2:38569621 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0232 |
2 | HG00738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1214+183G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569621 | |||||||
| chr2:38569751 | G | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0134 others(2): Show |
6 | HG00099.hp2 HG00735.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1214+53C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 9/12 | chr2 | 38569751 | |||||||
| chr2:38569978 | A | C | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-53T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38569978 | |||||||
| chr2:38570054 | T | TG | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(15): Show |
31 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1093-130dupC | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570054 | |||||||
| chr2:38570100 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1093-175T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570100 | |||||||
| chr2:38570134 | C | A | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-209G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570134 | |||||||
| chr2:38570161 | T | C | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-236A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570161 | |||||||
| chr2:38570193 | T | C | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1093-268A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570193 | |||||||
| chr2:38570232 | A | G | 34 | a0001c0001t0002g0009 a0001c0001t0002g0082 a0001c0001t0002g0095 others(31): Show |
46 | HG00140.hp2 HG00423.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1093-307T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570232 | |||||||
| chr2:38570345 | T | C | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-420A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570345 | |||||||
| chr2:38570468 | G | C | 1 | a0001c0001t0004g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1093-543C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570468 | |||||||
| chr2:38570493 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1093-568A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570493 | |||||||
| chr2:38570587 | T | C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(21): Show |
37 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1093-662A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570587 | |||||||
| chr2:38570864 | G | C | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-939C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570864 | |||||||
| chr2:38570879 | C | CA | 8 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(5): Show |
10 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1093-955dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570879 | |||||||
| chr2:38570918 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1093-993A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570918 | |||||||
| chr2:38570945 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG00639.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1093-1020C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38570945 | |||||||
| chr2:38571145 | T | C | 17 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(14): Show |
30 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1093-1220A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571145 | |||||||
| chr2:38571200 | G | GTTTAA | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1093-1276_1093-127 others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571200 | |||||||
| chr2:38571304 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1093-1379T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571304 | |||||||
| chr2:38571346 | CAGTG | C | 15 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(12): Show |
22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.1093-1425_1093-142 others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571346 | |||||||
| chr2:38571352 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1093-1427C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571352 | |||||||
| chr2:38571434 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1093-1509A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571434 | |||||||
| chr2:38571461 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1093-1536C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571461 | |||||||
| chr2:38571980 | G | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0162 a0001c0001t0002g0163 others(1): Show |
7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+1230C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38571980 | |||||||
| chr2:38572096 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1092+1114T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572096 | |||||||
| chr2:38572212 | A | ATGTTT | 102 | a0001c0001t0001g0048 a0001c0001t0001g0161 a0001c0001t0001g0166 others(99): Show |
140 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.1092+993_1092+997d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572212 | |||||||
| chr2:38572212 | A | ATGTTTTG others(3): Show |
2 | a0001c0001t0002g0016 a0001c0001t0011g0219 |
3 | HG00558.hp2 HG00621.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1092+988_1092+997d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572212 | |||||||
| chr2:38572341 | A | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+869T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572341 | |||||||
| chr2:38572400 | T | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0079 a0001c0001t0003g0083 others(1): Show |
7 | HG00597.hp1 HG02074.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+810A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572400 | |||||||
| chr2:38572410 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1092+800T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572410 | |||||||
| chr2:38572414 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0002g0058 a0001c0001t0002g0062 others(1): Show |
5 | NA18943.hp2 NA18986.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+796T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572414 | |||||||
| chr2:38572493 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0162 a0001c0001t0002g0163 others(1): Show |
7 | HG01106.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+717A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572493 | |||||||
| chr2:38572622 | T | C | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1092+588A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572622 | |||||||
| chr2:38572678 | G | A | 98 | a0001c0001t0001g0166 a0001c0001t0002g0003 a0001c0001t0002g0015 others(95): Show |
132 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1092+532C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572678 | |||||||
| chr2:38572695 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+515A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572695 | |||||||
| chr2:38572729 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0114 |
2 | NA18970.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1092+481C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572729 | |||||||
| chr2:38572754 | G | A | 37 | a0001c0001t0001g0166 a0001c0001t0002g0003 a0001c0001t0002g0015 others(34): Show |
48 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1092+456C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572754 | |||||||
| chr2:38572884 | C | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+326G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572884 | |||||||
| chr2:38572902 | A | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1092+308T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38572902 | |||||||
| chr2:38573192 | A | G | 19 | a0001c0001t0001g0158 a0001c0001t0002g0095 a0001c0001t0004g0033 others(16): Show |
27 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1092+18T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 8/12 | chr2 | 38573192 | |||||||
| chr2:38573462 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.875-35G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573462 | |||||||
| chr2:38573549 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.875-122A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573549 | |||||||
| chr2:38573671 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-244G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573671 | |||||||
| chr2:38573735 | C | T | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.875-308G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38573735 | |||||||
| chr2:38574105 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(176): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.875-678A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574105 | |||||||
| chr2:38574140 | A | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.875-713T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574140 | |||||||
| chr2:38574166 | A | G | 2 | a0001c0001t0007g0102 a0001c0001t0007g0164 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.875-739T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574166 | |||||||
| chr2:38574318 | A | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0005g0040 others(5): Show |
10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.875-891T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574318 | |||||||
| chr2:38574437 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.875-1010A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574437 | |||||||
| chr2:38574549 | CTAAG | C | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-1126_875-1123d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38574549 | |||||||
| chr2:38575018 | C | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1591G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575018 | |||||||
| chr2:38575022 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.875-1595A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575022 | |||||||
| chr2:38575203 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1776T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575203 | |||||||
| chr2:38575235 | TA | T | 2 | a0001c0001t0009g0024 a0001c0001t0009g0154 |
3 | HG02717.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.875-1809delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575235 | |||||||
| chr2:38575300 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.875-1873A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575300 | |||||||
| chr2:38575325 | A | T | 3 | a0001c0001t0011g0029 a0001c0001t0011g0218 a0001c0001t0011g0219 |
4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1898T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575325 | |||||||
| chr2:38575360 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.875-1933T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575360 | |||||||
| chr2:38575578 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.874+1883T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575578 | |||||||
| chr2:38575590 | G | C | 1 | a0001c0001t0002g0054 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.874+1871C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575590 | |||||||
| chr2:38575599 | C | T | 1 | a0001c0001t0002g0009 | 4 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+1862G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575599 | |||||||
| chr2:38575655 | C | A | 1 | a0001c0001t0007g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.874+1806G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575655 | |||||||
| chr2:38575760 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1701C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575760 | |||||||
| chr2:38575779 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.874+1682A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575779 | |||||||
| chr2:38575939 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1522T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38575939 | |||||||
| chr2:38576205 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1256A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576205 | |||||||
| chr2:38576268 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.874+1193T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576268 | |||||||
| chr2:38576307 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.874+1154G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576307 | |||||||
| chr2:38576360 | C | G | 8 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(5): Show |
10 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.874+1101G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576360 | |||||||
| chr2:38576577 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.874+884G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576577 | |||||||
| chr2:38576673 | T | C | 20 | a0001c0001t0001g0158 a0001c0001t0002g0056 a0001c0001t0002g0095 others(17): Show |
28 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.874+788A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576673 | |||||||
| chr2:38576713 | T | A | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.874+748A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576713 | |||||||
| chr2:38576777 | G | A | 2 | a0001c0001t0016g0101 a0001c0001t0016g0109 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.874+684C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576777 | |||||||
| chr2:38576989 | C | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0016 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.874+472G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38576989 | |||||||
| chr2:38577082 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.874+379A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577082 | |||||||
| chr2:38577311 | A | C | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(15): Show |
32 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.874+150T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577311 | |||||||
| chr2:38577334 | G | A | 2 | a0001c0001t0003g0079 a0001c0001t0003g0083 |
2 | NA18943.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.874+127C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 7/12 | chr2 | 38577334 | |||||||
| chr2:38577647 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.803-115G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577647 | |||||||
| chr2:38577671 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.803-139G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577671 | |||||||
| chr2:38577944 | A | G | 1 | a0001c0001t0011g0218 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.803-412T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38577944 | |||||||
| chr2:38578058 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.803-526G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578058 | |||||||
| chr2:38578143 | C | T | 1 | a0001c0001t0002g0231 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.803-611G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578143 | |||||||
| chr2:38578407 | G | C | 1 | a0001c0001t0004g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.803-875C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578407 | |||||||
| chr2:38578444 | A | G | 1 | a0001c0001t0004g0034 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.803-912T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578444 | |||||||
| chr2:38578454 | C | T | 109 | a0001c0001t0001g0166 a0001c0001t0002g0003 a0001c0001t0002g0015 others(106): Show |
145 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.803-922G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578454 | |||||||
| chr2:38578467 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.803-935T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578467 | |||||||
| chr2:38578643 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.803-1111G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578643 | |||||||
| chr2:38578881 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-1349G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38578881 | |||||||
| chr2:38579037 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.803-1505A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579037 | |||||||
| chr2:38579040 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.803-1508C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579040 | |||||||
| chr2:38579068 | T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.803-1536A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579068 | |||||||
| chr2:38579090 | C | A | 1 | a0001c0001t0001g0028 | 2 | NA19065.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.803-1558G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579090 | |||||||
| chr2:38579148 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-1616A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579148 | |||||||
| chr2:38579159 | G | C | 1 | a0001c0001t0002g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.803-1627C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579159 | |||||||
| chr2:38579187 | A | C | 47 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0166 others(44): Show |
59 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1655T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579187 | |||||||
| chr2:38579380 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1848C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579380 | |||||||
| chr2:38579390 | C | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1858G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579390 | |||||||
| chr2:38579391 | CTAAAACT others(1): Show |
C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1867_803-1860d others(10): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579391 | |||||||
| chr2:38579417 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.803-1885T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579417 | |||||||
| chr2:38579441 | T | C | 1 | a0001c0001t0012g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.803-1909A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579441 | |||||||
| chr2:38579489 | G | A | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.803-1957C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579489 | |||||||
| chr2:38579507 | G | A | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.803-1975C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579507 | |||||||
| chr2:38579715 | G | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(13): Show |
29 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.803-2183C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579715 | |||||||
| chr2:38579725 | TTTTAAAA others(9): Show |
T | 1 | a0002c0002t0006g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.802+2172_802+2187d others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579725 | |||||||
| chr2:38579729 | A | T | 2 | a0001c0001t0018g0108 a0001c0001t0019g0171 |
2 | HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.802+2184T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579729 | |||||||
| chr2:38579741 | A | AT | 98 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0149 others(95): Show |
133 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.802+2171dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579741 | |||||||
| chr2:38579741 | A | ATT | 7 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(4): Show |
7 | NA18945.hp2 NA18951.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+2170_802+2171d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579741 | |||||||
| chr2:38579750 | G | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0095 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2163C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579750 | |||||||
| chr2:38579752 | T | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0095 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2161A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579752 | |||||||
| chr2:38579754 | A | T | 2 | a0001c0001t0002g0061 a0001c0001t0002g0095 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.802+2159T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579754 | |||||||
| chr2:38579884 | A | G | 24 | a0001c0001t0001g0158 a0001c0001t0002g0095 a0001c0001t0004g0033 others(21): Show |
32 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.802+2029T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38579884 | |||||||
| chr2:38580035 | C | G | 40 | a0001c0001t0001g0166 a0001c0001t0002g0003 a0001c0001t0002g0015 others(37): Show |
51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.802+1878G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580035 | |||||||
| chr2:38580059 | C | T | 11 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 others(8): Show |
11 | HG02647.hp1 HG03130.hp2 HG03453.hp2 others(8): Show |
intron_variant | MODIFIER | c.802+1854G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580059 | |||||||
| chr2:38580131 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.802+1782A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580131 | |||||||
| chr2:38580164 | A | T | 15 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 others(12): Show |
16 | HG02647.hp1 HG02717.hp2 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+1749T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580164 | |||||||
| chr2:38580236 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.802+1677C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580236 | |||||||
| chr2:38580299 | G | A | 31 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(28): Show |
45 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.802+1614C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580299 | |||||||
| chr2:38580301 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.802+1612G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580301 | |||||||
| chr2:38580555 | T | C | 2 | a0001c0001t0001g0143 a0001c0005t0001g0144 |
2 | HG01192.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.802+1358A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580555 | |||||||
| chr2:38580764 | G | A | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.802+1149C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580764 | |||||||
| chr2:38580874 | T | C | 1 | a0001c0001t0005g0046 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.802+1039A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580874 | |||||||
| chr2:38580893 | T | C | 13 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(10): Show |
25 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+1020A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580893 | |||||||
| chr2:38580968 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802+945G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38580968 | |||||||
| chr2:38581115 | G | C | 1 | a0001c0001t0002g0235 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+798C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581115 | |||||||
| chr2:38581652 | GA | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0200 a0001c0001t0017g0191 |
3 | HG03492.hp2 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.802+260delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581652 | |||||||
| chr2:38581715 | A | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+198T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581715 | |||||||
| chr2:38581744 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.802+169T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 6/12 | chr2 | 38581744 | |||||||
| chr2:38582012 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.730-27A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/12 | chr2 | 38582012 | |||||||
| chr2:38582020 | C | T | 102 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(99): Show |
137 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.730-35G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 5/12 | chr2 | 38582020 | |||||||
| chr2:38582297 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.633-129A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582297 | |||||||
| chr2:38582388 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0020g0076 |
9 | HG00609.hp2 HG02155.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.633-220C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582388 | |||||||
| chr2:38582403 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0134 |
3 | HG00099.hp2 HG00735.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.633-235G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582403 | |||||||
| chr2:38582404 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.633-236C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582404 | |||||||
| chr2:38582441 | G | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633-273C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582441 | |||||||
| chr2:38582484 | A | AT | 5 | a0001c0001t0001g0081 a0001c0001t0001g0110 a0001c0001t0001g0119 others(2): Show |
5 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-317dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582484 | |||||||
| chr2:38582526 | T | C | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(15): Show |
32 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.633-358A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582526 | |||||||
| chr2:38582528 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-360A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582528 | |||||||
| chr2:38582557 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633-389C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582557 | |||||||
| chr2:38582599 | T | C | 46 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0149 others(43): Show |
58 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.633-431A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582599 | |||||||
| chr2:38582637 | T | A | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633-469A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582637 | |||||||
| chr2:38582669 | C | T | 1 | a0002c0002t0006g0249 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.633-501G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582669 | |||||||
| chr2:38582717 | C | G | 4 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0002c0002t0013g0035 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-549G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582717 | |||||||
| chr2:38582730 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-562C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582730 | |||||||
| chr2:38582756 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-588G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582756 | |||||||
| chr2:38582779 | G | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.633-611C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582779 | |||||||
| chr2:38582828 | G | A | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.633-660C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582828 | |||||||
| chr2:38582830 | G | C | 1 | a0001c0001t0002g0009 | 4 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-662C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582830 | |||||||
| chr2:38582862 | A | G | 105 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0001g0167 others(102): Show |
140 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.633-694T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582862 | |||||||
| chr2:38582874 | T | TA | 7 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 others(4): Show |
8 | HG02630.hp2 HG02647.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.633-707dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582874 | |||||||
| chr2:38582876 | A | C | 4 | a0001c0001t0010g0030 a0001c0001t0010g0229 a0001c0001t0010g0234 others(1): Show |
5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-708T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582876 | |||||||
| chr2:38582971 | G | A | 2 | a0001c0001t0016g0101 a0001c0001t0016g0109 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.633-803C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38582971 | |||||||
| chr2:38583022 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.632+819G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583022 | |||||||
| chr2:38583152 | A | AT | 4 | a0001c0001t0010g0030 a0001c0001t0010g0229 a0001c0001t0010g0234 others(1): Show |
5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+688dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583152 | |||||||
| chr2:38583152 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.632+689T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583152 | |||||||
| chr2:38583167 | A | T | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.632+674T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583167 | |||||||
| chr2:38583298 | C | A | 4 | a0001c0001t0010g0030 a0001c0001t0010g0229 a0001c0001t0010g0234 others(1): Show |
5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+543G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583298 | |||||||
| chr2:38583338 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0155 a0001c0001t0001g0156 others(5): Show |
13 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.632+503A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583338 | |||||||
| chr2:38583485 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.632+356T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583485 | |||||||
| chr2:38583679 | G | A | 41 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.632+162C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583679 | |||||||
| chr2:38583786 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0128 others(2): Show |
6 | HG01255.hp2 HG03831.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.632+55T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 4/12 | chr2 | 38583786 | |||||||
| chr2:38584077 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.547-151G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584077 | |||||||
| chr2:38584127 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.547-201A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584127 | |||||||
| chr2:38584178 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.547-252T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584178 | |||||||
| chr2:38584185 | C | T | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-259G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584185 | |||||||
| chr2:38584218 | C | T | 1 | a0001c0001t0012g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.547-292G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584218 | |||||||
| chr2:38584245 | A | G | 3 | a0001c0001t0007g0098 a0001c0001t0007g0102 a0001c0001t0007g0164 |
3 | HG02280.hp1 HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.547-319T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584245 | |||||||
| chr2:38584321 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-395T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584321 | |||||||
| chr2:38584396 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.547-470G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584396 | |||||||
| chr2:38584540 | T | A | 41 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.547-614A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584540 | |||||||
| chr2:38584687 | A | G | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.547-761T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584687 | |||||||
| chr2:38584750 | C | G | 5 | a0001c0001t0007g0098 a0001c0001t0007g0102 a0001c0001t0007g0164 others(2): Show |
5 | HG02280.hp1 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.547-824G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584750 | |||||||
| chr2:38584789 | T | G | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.546+855A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584789 | |||||||
| chr2:38584814 | TAA | T | 14 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0038 others(11): Show |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.546+828_546+829del others(2): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584814 | |||||||
| chr2:38584878 | T | G | 2 | a0001c0001t0010g0234 a0001c0001t0010g0237 |
2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.546+766A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584878 | |||||||
| chr2:38584971 | A | G | 2 | a0001c0001t0007g0078 a0001c0001t0007g0147 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.546+673T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38584971 | |||||||
| chr2:38585025 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.546+619A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585025 | |||||||
| chr2:38585036 | C | T | 1 | a0001c0001t0024g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.546+608G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585036 | |||||||
| chr2:38585074 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.546+570G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585074 | |||||||
| chr2:38585122 | GTAGGAAG others(5): Show |
G | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.546+510_546+521del others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585122 | |||||||
| chr2:38585356 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+288C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585356 | |||||||
| chr2:38585376 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0212 |
3 | NA18979.hp1 NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.546+268T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585376 | |||||||
| chr2:38585410 | G | A | 1 | a0001c0001t0016g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.546+234C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585410 | |||||||
| chr2:38585514 | A | G | 21 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0002g0003 others(18): Show |
29 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.546+130T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585514 | |||||||
| chr2:38585518 | T | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.546+126A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585518 | |||||||
| chr2:38585538 | A | G | 2 | a0001c0001t0016g0101 a0001c0001t0016g0109 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.546+106T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 3/12 | chr2 | 38585538 | |||||||
| chr2:38585948 | T | C | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.309-67A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38585948 | |||||||
| chr2:38586015 | C | G | 18 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(15): Show |
26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-134G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586015 | |||||||
| chr2:38586025 | C | CT | 9 | a0001c0001t0004g0246 a0002c0002t0006g0249 a0002c0002t0006g0250 others(6): Show |
9 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.309-145dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586025 | |||||||
| chr2:38586038 | TTGAGACG others(11): Show |
T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0225 |
3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-175_309-158del others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586038 | |||||||
| chr2:38586057 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0225 |
3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-176A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586057 | |||||||
| chr2:38586061 | G | A | 1 | a0001c0001t0002g0058 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309-180C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586061 | |||||||
| chr2:38586061 | G | T | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0225 |
3 | HG01106.hp1 HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.309-180C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586061 | |||||||
| chr2:38586062 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-181G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586062 | |||||||
| chr2:38586107 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309-226G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586107 | |||||||
| chr2:38586240 | C | G | 1 | a0001c0001t0014g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.309-359G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586240 | |||||||
| chr2:38586257 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.309-376C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586257 | |||||||
| chr2:38586273 | G | A | 18 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(15): Show |
26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-392C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586273 | |||||||
| chr2:38586299 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.309-418C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586299 | |||||||
| chr2:38586430 | T | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.309-549A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586430 | |||||||
| chr2:38586477 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0151 |
4 | HG02451.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.309-596C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586477 | |||||||
| chr2:38586560 | G | A | 12 | a0001c0001t0010g0030 a0001c0001t0010g0229 a0001c0001t0010g0234 others(9): Show |
13 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.309-679C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586560 | |||||||
| chr2:38586581 | C | A | 1 | a0001c0001t0022g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.309-700G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586581 | |||||||
| chr2:38586605 | T | C | 14 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0025 others(11): Show |
25 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.309-724A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586605 | |||||||
| chr2:38586634 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.309-753A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586634 | |||||||
| chr2:38586655 | T | G | 18 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(15): Show |
26 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.309-774A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586655 | |||||||
| chr2:38586757 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.309-876C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586757 | |||||||
| chr2:38586863 | A | G | 41 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0002g0003 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.309-982T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586863 | |||||||
| chr2:38586902 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.309-1021C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38586902 | |||||||
| chr2:38587049 | T | C | 4 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0002c0002t0013g0035 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.309-1168A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587049 | |||||||
| chr2:38587126 | T | G | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.309-1245A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587126 | |||||||
| chr2:38587177 | G | A | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309-1296C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587177 | |||||||
| chr2:38587284 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.309-1403T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587284 | |||||||
| chr2:38587313 | T | C | 2 | a0001c0001t0002g0082 a0001c0001t0018g0108 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.309-1432A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587313 | |||||||
| chr2:38587365 | ATTAT | A | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.309-1488_309-1485d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587365 | |||||||
| chr2:38587375 | G | A | 98 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(95): Show |
130 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.309-1494C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587375 | |||||||
| chr2:38587380 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.309-1499A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587380 | |||||||
| chr2:38587464 | C | T | 2 | a0001c0001t0002g0009 a0001c0001t0019g0171 |
5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.309-1583G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587464 | |||||||
| chr2:38587506 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.309-1625C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587506 | |||||||
| chr2:38587535 | C | T | 5 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0239 others(2): Show |
7 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-1654G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587535 | |||||||
| chr2:38587644 | G | GA | 20 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0025 others(17): Show |
30 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.309-1764dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587644 | |||||||
| chr2:38587691 | T | C | 15 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(12): Show |
22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.309-1810A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587691 | |||||||
| chr2:38587712 | T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.309-1831A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587712 | |||||||
| chr2:38587813 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.309-1932A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587813 | |||||||
| chr2:38587867 | G | A | 1 | a0001c0001t0017g0191 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.309-1986C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587867 | |||||||
| chr2:38587963 | T | G | 1 | a0001c0001t0002g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.309-2082A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587963 | |||||||
| chr2:38587975 | C | CT | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2095dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587975 | |||||||
| chr2:38587999 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2118A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38587999 | |||||||
| chr2:38588060 | G | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2179C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588060 | |||||||
| chr2:38588100 | G | A | 1 | a0001c0001t0023g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.309-2219C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588100 | |||||||
| chr2:38588107 | G | A | 33 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(30): Show |
50 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.309-2226C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588107 | |||||||
| chr2:38588119 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2238G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588119 | |||||||
| chr2:38588142 | C | T | 1 | a0001c0001t0009g0152 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.309-2261G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588142 | |||||||
| chr2:38588164 | T | C | 11 | a0001c0001t0016g0101 a0001c0001t0016g0109 a0001c0001t0018g0108 others(8): Show |
11 | HG02630.hp2 HG02922.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.309-2283A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588164 | |||||||
| chr2:38588222 | T | C | 42 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0166 others(39): Show |
53 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.309-2341A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588222 | |||||||
| chr2:38588245 | G | C | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.309-2364C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588245 | |||||||
| chr2:38588420 | G | T | 1 | a0002c0002t0006g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.309-2539C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588420 | |||||||
| chr2:38588505 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.309-2624G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588505 | |||||||
| chr2:38588542 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.309-2661T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588542 | |||||||
| chr2:38588546 | C | CA | 15 | a0001c0001t0001g0074 a0001c0001t0001g0126 a0001c0001t0001g0141 others(12): Show |
15 | HG00673.hp1 HG01358.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.309-2666dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAA | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0106 others(7): Show |
15 | HG01255.hp2 HG02109.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.309-2667_309-2666d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAA | 5 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.309-2671_309-2666d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA | 16 | a0001c0001t0001g0091 a0001c0001t0002g0009 a0001c0001t0002g0017 others(13): Show |
21 | HG00639.hp1 HG00738.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.309-2672_309-2666d others(9): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(1): Show |
18 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0143 others(15): Show |
22 | HG01070.hp1 HG01106.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.309-2673_309-2666d others(10): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(2): Show |
15 | a0001c0001t0002g0032 a0001c0001t0002g0071 a0001c0001t0002g0235 others(12): Show |
23 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.309-2674_309-2666d others(11): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0004g0243 a0003c0003t0004g0244 a0003c0003t0004g0245 |
3 | NA18940.hp1 NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.309-2675_309-2666d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.309-2677_309-2666d others(14): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0167 |
2 | HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.309-2679_309-2666d others(16): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0168 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.309-2680_309-2666d others(17): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.309-2681_309-2666d others(18): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(12): Show |
2 | a0002c0002t0006g0249 a0002c0002t0006g0250 |
2 | NA18951.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.309-2684_309-2666d others(21): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(13): Show |
1 | a0002c0002t0006g0251 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.309-2685_309-2666d others(22): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(24): Show |
1 | a0002c0002t0006g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.309-2666_309-2665i others(33): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(25): Show |
2 | a0002c0002t0006g0253 a0002c0002t0006g0256 |
2 | NA18950.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.309-2666_309-2665i others(34): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | C | CAAAAAAA others(29): Show |
2 | a0002c0002t0006g0254 a0002c0002t0006g0255 |
2 | NA18994.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.309-2666_309-2665i others(38): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | CAAAA | C | 12 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0025 others(9): Show |
22 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.309-2669_309-2666d others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | CAAAAA | C | 10 | a0001c0001t0007g0078 a0001c0001t0007g0098 a0001c0001t0007g0102 others(7): Show |
11 | HG01496.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.309-2670_309-2666d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588546 | CAAAAAAA others(3): Show |
C | 24 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(21): Show |
32 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.309-2675_309-2666d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588546 | |||||||
| chr2:38588591 | A | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.309-2710T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588591 | |||||||
| chr2:38588726 | G | GT | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2803dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588726 | |||||||
| chr2:38588754 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.308+2776T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588754 | |||||||
| chr2:38588835 | G | C | 1 | a0002c0002t0006g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.308+2695C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588835 | |||||||
| chr2:38588876 | C | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2654G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588876 | |||||||
| chr2:38588889 | C | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2641G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588889 | |||||||
| chr2:38588932 | T | C | 37 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(34): Show |
55 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.308+2598A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588932 | |||||||
| chr2:38588993 | T | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+2537A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38588993 | |||||||
| chr2:38589035 | A | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0168 |
2 | HG01099.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.308+2495T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589035 | |||||||
| chr2:38589125 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.308+2405G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589125 | |||||||
| chr2:38589219 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+2311T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589219 | |||||||
| chr2:38589258 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.308+2272T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589258 | |||||||
| chr2:38589677 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1853C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589677 | |||||||
| chr2:38589766 | A | C | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1764T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589766 | |||||||
| chr2:38589782 | C | A | 4 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.308+1748G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589782 | |||||||
| chr2:38589844 | T | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1686A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589844 | |||||||
| chr2:38589845 | T | G | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1685A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589845 | |||||||
| chr2:38589879 | T | C | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.308+1651A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38589879 | |||||||
| chr2:38590070 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+1460A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590070 | |||||||
| chr2:38590184 | T | C | 15 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(12): Show |
22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.308+1346A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590184 | |||||||
| chr2:38590260 | C | T | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+1270G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590260 | |||||||
| chr2:38590272 | G | C | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.308+1258C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590272 | |||||||
| chr2:38590448 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.308+1082A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590448 | |||||||
| chr2:38590641 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0019g0171 |
5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+889C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590641 | |||||||
| chr2:38590844 | A | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+686T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590844 | |||||||
| chr2:38590862 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+668C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590862 | |||||||
| chr2:38590967 | T | C | 1 | a0001c0001t0007g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.308+563A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590967 | |||||||
| chr2:38590986 | C | CAG | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+542_308+543dup others(2): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590986 | |||||||
| chr2:38590997 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.308+533G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38590997 | |||||||
| chr2:38591079 | C | T | 97 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0166 others(94): Show |
129 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.308+451G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591079 | |||||||
| chr2:38591108 | C | T | 41 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0002g0003 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.308+422G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591108 | |||||||
| chr2:38591229 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.308+301G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591229 | |||||||
| chr2:38591283 | T | C | 34 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(31): Show |
51 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.308+247A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591283 | |||||||
| chr2:38591352 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0019g0171 |
5 | HG02723.hp1 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+178C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591352 | |||||||
| chr2:38591406 | T | C | 3 | a0001c0001t0008g0192 a0001c0001t0008g0193 a0001c0001t0008g0208 |
3 | NA18956.hp1 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.308+124A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591406 | |||||||
| chr2:38591459 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.308+71C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591459 | |||||||
| chr2:38591503 | T | G | 2 | a0001c0001t0007g0102 a0001c0001t0007g0164 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.308+27A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 2/12 | chr2 | 38591503 | |||||||
| chr2:38591678 | A | C | 7 | a0001c0001t0004g0242 a0001c0001t0004g0243 a0001c0001t0004g0246 others(4): Show |
12 | HG00423.hp2 NA18940.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-30T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591678 | |||||||
| chr2:38591698 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-50C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591698 | |||||||
| chr2:38591833 | A | G | 40 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(37): Show |
51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.190-185T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591833 | |||||||
| chr2:38591840 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.190-192C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591840 | |||||||
| chr2:38591902 | G | A | 15 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(12): Show |
22 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-254C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591902 | |||||||
| chr2:38591907 | T | C | 2 | a0001c0001t0007g0147 a0001c0001t0007g0228 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-259A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591907 | |||||||
| chr2:38591951 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-303C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591951 | |||||||
| chr2:38591972 | T | A | 1 | a0001c0001t0005g0046 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.190-324A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591972 | |||||||
| chr2:38591975 | C | CA | 5 | a0001c0001t0001g0096 a0001c0001t0009g0024 a0001c0001t0009g0152 others(2): Show |
6 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-328dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38591975 | |||||||
| chr2:38592001 | T | C | 2 | a0001c0001t0007g0147 a0001c0001t0007g0228 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-353A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592001 | |||||||
| chr2:38592099 | A | G | 1 | a0001c0001t0004g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.190-451T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592099 | |||||||
| chr2:38592180 | A | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.190-532T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592180 | |||||||
| chr2:38592279 | A | AGTTGTT | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-632_190-631ins others(6): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592279 | |||||||
| chr2:38592328 | C | T | 40 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(37): Show |
51 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.190-680G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592328 | |||||||
| chr2:38592384 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.190-736C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592384 | |||||||
| chr2:38592418 | G | A | 1 | a0001c0001t0008g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.190-770C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592418 | |||||||
| chr2:38592440 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.190-792A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592440 | |||||||
| chr2:38592499 | A | G | 16 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(13): Show |
16 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.190-851T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592499 | |||||||
| chr2:38592523 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190-875C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592523 | |||||||
| chr2:38592557 | C | G | 55 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(52): Show |
70 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.190-909G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592557 | |||||||
| chr2:38592565 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.190-917G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592565 | |||||||
| chr2:38592604 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.190-956C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592604 | |||||||
| chr2:38592627 | T | C | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-979A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592627 | |||||||
| chr2:38592636 | A | G | 1 | a0001c0001t0005g0042 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.190-988T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592636 | |||||||
| chr2:38592764 | G | A | 41 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(38): Show |
52 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.190-1116C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592764 | |||||||
| chr2:38592765 | T | C | 4 | a0001c0001t0010g0030 a0001c0001t0010g0229 a0001c0001t0010g0234 others(1): Show |
5 | HG01496.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1117A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592765 | |||||||
| chr2:38592801 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.190-1153A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592801 | |||||||
| chr2:38592809 | A | G | 1 | a0001c0001t0002g0049 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.190-1161T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592809 | |||||||
| chr2:38592860 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.190-1212G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592860 | |||||||
| chr2:38592958 | T | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-1310A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592958 | |||||||
| chr2:38592970 | A | G | 4 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0235 others(1): Show |
6 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-1322T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38592970 | |||||||
| chr2:38593036 | T | C | 11 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0077 others(8): Show |
21 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-1388A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593036 | |||||||
| chr2:38593289 | T | C | 36 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(33): Show |
54 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.190-1641A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593289 | |||||||
| chr2:38593295 | T | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1647A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593295 | |||||||
| chr2:38593380 | T | C | 67 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0166 others(64): Show |
82 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.190-1732A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593380 | |||||||
| chr2:38593393 | T | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG00597.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.190-1745A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593393 | |||||||
| chr2:38593414 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1766A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593414 | |||||||
| chr2:38593420 | G | C | 4 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0002c0002t0013g0035 others(1): Show |
5 | HG01106.hp2 HG01891.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-1772C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593420 | |||||||
| chr2:38593536 | A | G | 1 | a0001c0001t0023g0047 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.190-1888T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593536 | |||||||
| chr2:38593603 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-1955A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593603 | |||||||
| chr2:38593800 | C | T | 19 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0077 others(16): Show |
29 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.190-2152G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593800 | |||||||
| chr2:38593858 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-2210C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593858 | |||||||
| chr2:38593862 | C | CA | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(176): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.190-2215dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | |||||||
| chr2:38593862 | C | CAA | 11 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0077 others(8): Show |
21 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.190-2216_190-2215d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | |||||||
| chr2:38593862 | C | CAAA | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2217_190-2215d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593862 | |||||||
| chr2:38593873 | C | A | 9 | a0001c0001t0001g0149 a0002c0002t0006g0249 a0002c0002t0006g0250 others(6): Show |
9 | HG02056.hp1 NA18945.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-2225G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593873 | |||||||
| chr2:38593881 | A | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-2233T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593881 | |||||||
| chr2:38593882 | A | C | 1 | a0001c0001t0012g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.190-2234T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38593882 | |||||||
| chr2:38594031 | C | T | 1 | a0001c0001t0018g0108 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.190-2383G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594031 | |||||||
| chr2:38594082 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.190-2434C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594082 | |||||||
| chr2:38594174 | C | CA | 5 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0217 others(2): Show |
5 | HG02074.hp1 HG02273.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-2527dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594174 | |||||||
| chr2:38594192 | CA | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2545delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594192 | |||||||
| chr2:38594199 | C | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2551G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594199 | |||||||
| chr2:38594210 | A | C | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(12): Show |
19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-2562T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594210 | |||||||
| chr2:38594332 | A | G | 1 | a0001c0001t0003g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.190-2684T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594332 | |||||||
| chr2:38594371 | G | A | 114 | a0001c0001t0001g0048 a0001c0001t0001g0091 a0001c0001t0001g0092 others(111): Show |
150 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.190-2723C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594371 | |||||||
| chr2:38594423 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.190-2775C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594423 | |||||||
| chr2:38594477 | A | T | 3 | a0001c0001t0002g0009 a0001c0001t0007g0098 a0001c0001t0019g0171 |
6 | HG02280.hp1 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-2829T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594477 | |||||||
| chr2:38594550 | A | G | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.190-2902T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594550 | |||||||
| chr2:38594569 | G | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-2921C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594569 | |||||||
| chr2:38594747 | C | T | 8 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0005g0040 others(5): Show |
10 | HG01070.hp1 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-3099G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594747 | |||||||
| chr2:38594755 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(252): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.190-3107T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594755 | |||||||
| chr2:38594795 | G | C | 9 | a0001c0001t0007g0098 a0002c0002t0006g0249 a0002c0002t0006g0250 others(6): Show |
9 | HG02280.hp1 NA18945.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-3147C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594795 | |||||||
| chr2:38594853 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.190-3205T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594853 | |||||||
| chr2:38594871 | T | C | 1 | a0001c0001t0012g0133 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.190-3223A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594871 | |||||||
| chr2:38594871 | T | G | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-3223A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594871 | |||||||
| chr2:38594933 | C | A | 14 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(11): Show |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.190-3285G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38594933 | |||||||
| chr2:38595014 | T | C | 19 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0077 others(16): Show |
29 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.190-3366A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595014 | |||||||
| chr2:38595107 | C | T | 1 | a0001c0001t0007g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-3459G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595107 | |||||||
| chr2:38595250 | G | A | 1 | a0003c0003t0004g0245 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.190-3602C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595250 | |||||||
| chr2:38595272 | T | TA | 29 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0001g0134 others(26): Show |
29 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.190-3625dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595272 | TA | T | 17 | a0001c0001t0001g0093 a0001c0001t0001g0103 a0001c0001t0001g0104 others(14): Show |
17 | HG00323.hp1 HG00323.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-3625delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595272 | TAA | T | 33 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0002g0031 others(30): Show |
46 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.190-3626_190-3625d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595272 | TAAA | T | 39 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0002g0003 others(36): Show |
50 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.190-3627_190-3625d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595272 | TAAAAAA | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-3630_190-3625d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595272 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0021g0238 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.190-3634_190-3625d others(12): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595272 | |||||||
| chr2:38595276 | A | T | 1 | a0001c0001t0024g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.190-3628T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595276 | |||||||
| chr2:38595292 | A | G | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(12): Show |
19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.190-3644T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595292 | |||||||
| chr2:38595293 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | NA18970.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.190-3645T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595293 | |||||||
| chr2:38595294 | A | G | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-3646T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595294 | |||||||
| chr2:38595308 | A | C | 2 | a0001c0001t0002g0041 a0001c0001t0005g0040 |
2 | HG01169.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.190-3660T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595308 | |||||||
| chr2:38595310 | A | ACAC | 38 | a0001c0001t0001g0048 a0001c0001t0001g0166 a0001c0001t0002g0003 others(35): Show |
49 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.190-3665_190-3663d others(5): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595310 | |||||||
| chr2:38595310 | A | C | 2 | a0001c0001t0002g0041 a0001c0001t0005g0040 |
2 | HG01169.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.190-3662T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595310 | |||||||
| chr2:38595370 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.190-3722A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595370 | |||||||
| chr2:38595582 | C | T | 1 | a0001c0001t0007g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-3934G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595582 | |||||||
| chr2:38595583 | G | A | 6 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG00639.hp1 HG01192.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-3935C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595583 | |||||||
| chr2:38595613 | G | C | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-3965C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595613 | |||||||
| chr2:38595700 | C | T | 3 | a0001c0001t0011g0029 a0001c0001t0011g0218 a0001c0001t0011g0219 |
4 | HG01361.hp1 HG02486.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-4052G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595700 | |||||||
| chr2:38595701 | G | A | 14 | a0001c0001t0002g0095 a0001c0001t0004g0033 a0001c0001t0004g0034 others(11): Show |
21 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.190-4053C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595701 | |||||||
| chr2:38595713 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4065C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595713 | |||||||
| chr2:38595776 | A | G | 44 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0149 others(41): Show |
55 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.190-4128T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595776 | |||||||
| chr2:38595812 | C | G | 1 | a0001c0001t0007g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-4164G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595812 | |||||||
| chr2:38595839 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4191C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595839 | |||||||
| chr2:38595843 | C | CA | 13 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0239 others(10): Show |
20 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.190-4196dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595843 | |||||||
| chr2:38595939 | C | A | 10 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(7): Show |
19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.190-4291G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595939 | |||||||
| chr2:38595988 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.190-4340C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595988 | |||||||
| chr2:38595993 | T | C | 10 | a0001c0001t0002g0095 a0001c0001t0003g0004 a0001c0001t0003g0008 others(7): Show |
19 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.190-4345A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38595993 | |||||||
| chr2:38596069 | TA | T | 11 | a0001c0001t0001g0097 a0002c0002t0006g0249 a0002c0002t0006g0250 others(8): Show |
12 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-4422delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596069 | |||||||
| chr2:38596236 | G | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-4588C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596236 | |||||||
| chr2:38596342 | C | CCT | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(242): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.190-4696_190-4695d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596342 | |||||||
| chr2:38596434 | G | GT | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-4787dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596434 | |||||||
| chr2:38596463 | T | G | 23 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0239 others(20): Show |
31 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.190-4815A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596463 | |||||||
| chr2:38596481 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.190-4833A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596481 | |||||||
| chr2:38596482 | T | G | 3 | a0001c0001t0007g0078 a0001c0001t0007g0147 a0001c0001t0007g0228 |
3 | HG02647.hp1 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.190-4834A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596482 | |||||||
| chr2:38596526 | G | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190-4878C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596526 | |||||||
| chr2:38596527 | G | C | 1 | a0001c0001t0022g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.190-4879C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596527 | |||||||
| chr2:38596540 | G | A | 2 | a0001c0001t0002g0039 a0001c0001t0002g0065 |
2 | HG00673.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.190-4892C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596540 | |||||||
| chr2:38596712 | T | C | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.190-5064A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596712 | |||||||
| chr2:38596735 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.190-5087C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596735 | |||||||
| chr2:38596800 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190-5152G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596800 | |||||||
| chr2:38596856 | C | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-5208G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38596856 | |||||||
| chr2:38597145 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+5293A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597145 | |||||||
| chr2:38597233 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+5205T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597233 | |||||||
| chr2:38597268 | T | C | 1 | a0001c0001t0012g0148 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.189+5170A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597268 | |||||||
| chr2:38597287 | C | G | 1 | a0001c0001t0002g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.189+5151G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597287 | |||||||
| chr2:38597386 | CAAGAAT | C | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+5046_189+5051d others(8): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597386 | |||||||
| chr2:38597501 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.189+4937G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597501 | |||||||
| chr2:38597578 | A | G | 1 | a0001c0001t0004g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.189+4860T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597578 | |||||||
| chr2:38597584 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4854T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597584 | |||||||
| chr2:38597632 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0212 |
5 | NA18979.hp1 NA19009.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4806C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597632 | |||||||
| chr2:38597639 | T | A | 43 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0001g0149 others(40): Show |
54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+4799A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597639 | |||||||
| chr2:38597671 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+4767A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597671 | |||||||
| chr2:38597680 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.189+4758A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597680 | |||||||
| chr2:38597683 | C | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+4755G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597683 | |||||||
| chr2:38597691 | A | AT | 22 | a0001c0001t0002g0009 a0001c0001t0002g0057 a0001c0001t0004g0033 others(19): Show |
29 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.189+4746dupA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597691 | |||||||
| chr2:38597691 | AT | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(64): Show |
87 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.189+4746delA | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597691 | |||||||
| chr2:38597693 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0151 |
4 | HG02451.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4745A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597693 | |||||||
| chr2:38597697 | T | A | 4 | a0001c0001t0009g0024 a0001c0001t0009g0152 a0001c0001t0009g0153 others(1): Show |
5 | HG02717.hp2 HG02723.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4741A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597697 | |||||||
| chr2:38597751 | C | T | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4687G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597751 | |||||||
| chr2:38597771 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.189+4667G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597771 | |||||||
| chr2:38597835 | G | A | 11 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(8): Show |
14 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4603C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597835 | |||||||
| chr2:38597950 | T | C | 1 | a0001c0001t0008g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189+4488A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597950 | |||||||
| chr2:38597966 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+4472G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597966 | |||||||
| chr2:38597983 | G | A | 42 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(39): Show |
53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4455C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38597983 | |||||||
| chr2:38598057 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG01106.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.189+4381G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598057 | |||||||
| chr2:38598079 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+4359A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598079 | |||||||
| chr2:38598101 | AAAAAC | A | 42 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(39): Show |
53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4332_189+4336d others(7): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598101 | |||||||
| chr2:38598211 | G | A | 9 | a0001c0001t0003g0004 a0001c0001t0003g0008 a0001c0001t0003g0077 others(6): Show |
18 | HG00609.hp2 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.189+4227C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598211 | |||||||
| chr2:38598256 | T | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
14 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4182A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598256 | |||||||
| chr2:38598265 | G | C | 42 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(39): Show |
53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+4173C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598265 | |||||||
| chr2:38598267 | G | A | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+4171C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598267 | |||||||
| chr2:38598543 | A | T | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+3895T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598543 | |||||||
| chr2:38598557 | G | A | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3881C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598557 | |||||||
| chr2:38598558 | A | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3880T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598558 | |||||||
| chr2:38598582 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.189+3856C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598582 | |||||||
| chr2:38598639 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+3799A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598639 | |||||||
| chr2:38598874 | G | A | 1 | a0001c0001t0024g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189+3564C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598874 | |||||||
| chr2:38598902 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.189+3536T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598902 | |||||||
| chr2:38598972 | G | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01106.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.189+3466C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38598972 | |||||||
| chr2:38599005 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189+3433C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599005 | |||||||
| chr2:38599049 | C | G | 1 | a0001c0001t0004g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.189+3389G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599049 | |||||||
| chr2:38599049 | C | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+3389G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599049 | |||||||
| chr2:38599063 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.189+3375T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599063 | |||||||
| chr2:38599087 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.189+3351A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599087 | |||||||
| chr2:38599444 | G | A | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+2994C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599444 | |||||||
| chr2:38599557 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+2881G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599557 | |||||||
| chr2:38599561 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189+2877T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599561 | |||||||
| chr2:38599611 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.189+2827C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599611 | |||||||
| chr2:38599695 | C | T | 1 | a0001c0001t0014g0094 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.189+2743G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599695 | |||||||
| chr2:38599731 | CTA | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG00639.hp1 HG02257.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.189+2705_189+2706d others(4): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599731 | |||||||
| chr2:38599753 | C | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+2685G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599753 | |||||||
| chr2:38599758 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.189+2680G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599758 | |||||||
| chr2:38599783 | T | C | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(12): Show |
19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+2655A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599783 | |||||||
| chr2:38599928 | G | A | 1 | a0001c0001t0019g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+2510C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38599928 | |||||||
| chr2:38600009 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+2429C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600009 | |||||||
| chr2:38600019 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189+2419T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600019 | |||||||
| chr2:38600124 | T | G | 1 | a0001c0001t0007g0164 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189+2314A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600124 | |||||||
| chr2:38600217 | C | G | 1 | a0001c0001t0022g0037 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.189+2221G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600217 | |||||||
| chr2:38600242 | A | G | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+2196T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600242 | |||||||
| chr2:38600292 | C | A | 1 | a0001c0001t0004g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.189+2146G>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600292 | |||||||
| chr2:38600292 | CG | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(58): Show |
80 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+2145delC | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600292 | |||||||
| chr2:38600315 | A | G | 13 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0008 others(10): Show |
25 | HG00597.hp1 HG00609.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.189+2123T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600315 | |||||||
| chr2:38600637 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189+1801C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600637 | |||||||
| chr2:38600648 | G | A | 1 | a0001c0001t0004g0034 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.189+1790C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600648 | |||||||
| chr2:38600687 | C | T | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1751G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600687 | |||||||
| chr2:38600749 | C | CA | 17 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(14): Show |
18 | HG00140.hp1 HG01099.hp1 HG03139.hp2 others(15): Show |
intron_variant | MODIFIER | c.189+1688dupT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600749 | |||||||
| chr2:38600749 | CA | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0172 others(3): Show |
6 | HG01081.hp2 HG02145.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1688delT | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600749 | |||||||
| chr2:38600768 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.189+1670A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600768 | |||||||
| chr2:38600770 | T | C | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+1668A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600770 | |||||||
| chr2:38600811 | T | C | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1627A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600811 | |||||||
| chr2:38600823 | C | G | 43 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0002g0003 others(40): Show |
54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+1615G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600823 | |||||||
| chr2:38600884 | A | C | 4 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1554T>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38600884 | |||||||
| chr2:38601115 | C | CG | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1322_189+1323i others(3): Show |
HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601115 | |||||||
| chr2:38601189 | A | G | 2 | a0001c0001t0007g0078 a0001c0001t0007g0228 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.189+1249T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601189 | |||||||
| chr2:38601229 | T | C | 10 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(7): Show |
11 | NA18906.hp1 NA18945.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+1209A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601229 | |||||||
| chr2:38601362 | T | A | 7 | a0001c0001t0002g0017 a0001c0001t0002g0067 a0001c0001t0002g0068 others(4): Show |
8 | HG02280.hp2 HG02559.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.189+1076A>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601362 | |||||||
| chr2:38601375 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0077 a0001c0001t0020g0076 |
9 | HG00609.hp2 HG02155.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+1063T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601375 | |||||||
| chr2:38601396 | G | A | 42 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0015 others(39): Show |
53 | HG00558.hp2 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189+1042C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601396 | |||||||
| chr2:38601464 | A | G | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+974T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601464 | |||||||
| chr2:38601561 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189+877T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601561 | |||||||
| chr2:38601581 | G | A | 1 | a0001c0001t0019g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.189+857C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601581 | |||||||
| chr2:38601654 | G | A | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+784C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601654 | |||||||
| chr2:38601677 | T | C | 1 | a0001c0001t0010g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189+761A>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601677 | |||||||
| chr2:38601695 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(58): Show |
80 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.189+743C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601695 | |||||||
| chr2:38601719 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.189+719T>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601719 | |||||||
| chr2:38601719 | A | T | 4 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 others(1): Show |
4 | HG00738.hp1 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+719T>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601719 | |||||||
| chr2:38601809 | G | C | 15 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(12): Show |
19 | HG00738.hp1 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+629C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601809 | |||||||
| chr2:38601815 | G | T | 1 | a0001c0001t0010g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.189+623C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601815 | |||||||
| chr2:38601859 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+579C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601859 | |||||||
| chr2:38601897 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0004g0247 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.189+541A>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38601897 | |||||||
| chr2:38602028 | G | A | 7 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(4): Show |
7 | HG01106.hp1 HG01175.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+410C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602028 | |||||||
| chr2:38602061 | G | A | 8 | a0002c0002t0006g0249 a0002c0002t0006g0250 a0002c0002t0006g0251 others(5): Show |
8 | NA18945.hp2 NA18950.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+377C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602061 | |||||||
| chr2:38602132 | C | G | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+306G>C | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602132 | |||||||
| chr2:38602139 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0002g0073 |
3 | HG00423.hp1 NA18945.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.189+299G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602139 | |||||||
| chr2:38602148 | G | T | 2 | a0002c0002t0013g0035 a0002c0002t0013g0248 |
3 | NA18906.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.189+290C>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602148 | |||||||
| chr2:38602253 | C | T | 43 | a0001c0001t0001g0036 a0001c0001t0001g0048 a0001c0001t0002g0003 others(40): Show |
54 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.189+185G>A | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602253 | |||||||
| chr2:38602268 | G | A | 1 | a0001c0001t0007g0228 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.189+170C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602268 | |||||||
| chr2:38602346 | G | C | 12 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0230 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.189+92C>G | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602346 | |||||||
| chr2:38602420 | G | A | 13 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0239 others(10): Show |
20 | HG00140.hp2 HG00423.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.189+18C>T | HNRNPLL | ENSG00000143889.16 | transcript | ENST00000449105.8 | protein_coding | 1/12 | chr2 | 38602420 |