Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8178 |
| ensemblid | ENSG00000105656.13 |
| hgncid | 23114 |
| symbol | ELL |
| name | elongation factor for RNA polymerase II |
| refseq_nuc | NM_006532.4 |
| refseq_prot | NP_006523.1 |
| ensembl_nuc | ENST00000262809.9 |
| ensembl_prot | ENSP00000262809.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 18442663 |
| end | 18522070 |
| strand | - |
| ver | v1.2 |
| region | chr19:18442663-18522070 |
| region5000 | chr19:18437663-18527070 |
| regionname0 | ELL_chr19_18442663_18522070 |
| regionname5000 | ELL_chr19_18437663_18527070 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 621 | 195 | 68 | 60 | 38 | 8 | 19 | 30 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0002 | 0/0 | 621 | 43 | 22 | 6 | 5 | 2 | 8 | 3 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0003 | 0/0 | 621 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0004 | 0/0 | 621 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0005 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0006 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| a0007 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | MAALK others(616): Show |
chr19 | 18437663 | 18527070 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1863 | 181 | 55 | 60 | 38 | 8 | 18 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0003 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0004 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0005 | 0/0 | 1863 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0007 | 0/0 | 1863 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0010 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0012 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0001c0013 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0002c0002 | 0/0 | 1863 | 43 | 22 | 6 | 5 | 2 | 8 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0003c0006 | 0/0 | 1863 | 2 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0004c0008 | 0/0 | 1863 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0005c0011 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0006c0009 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 | ||
| a0007c0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | ATGGC others(1858): Show |
chr19 | 18437663 | 18527070 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3967 | 78 | 34 | 22 | 16 | 3 | 3 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0002 | 1/1 | 3970 | 84 | 8 | 33 | 22 | 4 | 15 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0003 | 0/0 | 3970 | 7 | 6 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0004 | 0/0 | 3967 | 5 | 3 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0011 | 0/0 | 3968 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3963): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0012 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0014 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0015 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0016 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0017 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0001t0018 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0003t0001 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0004t0006 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0005t0007 | 0/0 | 3967 | 3 | 3 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0007t0009 | 0/0 | 3967 | 2 | 2 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0010t0002 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0001c0012t0010 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0001c0013t0001 | 0/0 | 3967 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0002c0002t0001 | 0/0 | 3967 | 35 | 17 | 3 | 5 | 2 | 8 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0002c0002t0005 | 0/0 | 3967 | 4 | 4 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0002c0002t0008 | 0/0 | 3967 | 2 | 0 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0002c0002t0013 | 0/0 | 3967 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0002c0002t0019 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0003c0006t0001 | 0/0 | 3967 | 2 | 0 | 1 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0004c0008t0002 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0005c0011t0001 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| a0006c0009t0002 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3965): Show |
chr19 | 18437663 | 18527070 |
| a0007c0014t0001 | 0/0 | 3967 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | AGAGA others(3962): Show |
chr19 | 18437663 | 18527070 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0012g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0014g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0015g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0016g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0017g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0004t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0004t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0004t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0005t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0005t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0005t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0007t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0007t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0010t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0012t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0001c0013t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0013g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0002c0002t0019g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0003c0006t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0003c0006t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0004c0008t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0005c0011t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0006c0009t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| a0007c0014t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0238 | EUR | FIN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00639 | hp2 | a0004 | c0008 | t0002 | g0059 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0228 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01346 | hp2 | a0002 | c0002 | t0008 | g0118 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01496 | hp1 | a0002 | c0002 | t0013 | g0113 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01516 | hp1 | a0001 | c0001 | t0018 | g0196 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01884 | hp2 | a0002 | c0002 | t0019 | g0131 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01975 | hp1 | a0001 | c0001 | t0015 | g0065 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02004 | hp1 | a0002 | c0002 | t0008 | g0116 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02004 | hp2 | a0003 | c0006 | t0001 | g0208 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | CDX | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CDX | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0143 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02572 | hp2 | a0002 | c0002 | t0005 | g0120 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02615 | hp1 | a0002 | c0002 | t0005 | g0127 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02622 | hp1 | a0001 | c0005 | t0007 | g0174 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02647 | hp1 | a0001 | c0005 | t0007 | g0175 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0119 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02738 | hp2 | a0001 | c0013 | t0001 | g0207 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02886 | hp1 | a0001 | c0004 | t0006 | g0172 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02896 | hp1 | a0001 | c0005 | t0007 | g0176 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0162 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0240 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0173 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03041 | hp2 | a0001 | c0004 | t0006 | g0171 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0163 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0189 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03486 | hp1 | a0001 | c0012 | t0010 | g0165 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0115 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | GWD | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03654 | hp1 | a0003 | c0006 | t0001 | g0211 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0241 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | STU | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0239 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18522 | hp2 | a0001 | c0007 | t0009 | g0008 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | CHB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18906 | hp1 | a0005 | c0011 | t0001 | g0159 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18906 | hp2 | a0001 | c0004 | t0006 | g0170 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19030 | hp2 | a0001 | c0010 | t0002 | g0032 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19060 | hp2 | a0006 | c0009 | t0002 | g0069 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19240 | hp1 | a0001 | c0007 | t0009 | g0009 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ASW | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0124 | EUR | TSI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | GIH | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0197 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03471 | hp1 | a0002 | c0002 | t0005 | g0121 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20300 | hp1 | a0007 | c0014 | t0001 | g0013 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | USA | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | LWK | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0038 | REF | REF | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0063 | REF | REF | ELL_chr19_18437663_18527070 | ELL | chr19 | 18437663 | 18527070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18446370 | C | T | 1 | a0005 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.1643G>A | p.Arg548Gln | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/12 | 1658/3970 | 1643/1866 | 548/621 | chr19 | 18446370 | |||
| chr19:18450785 | G | A | 1 | a0007 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1157C>T | p.Pro386Leu | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1172/3970 | 1157/1866 | 386/621 | chr19 | 18450785 | |||
| chr19:18451628 | C | T | 1 | a0002 | 43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
missense_variant | MODERATE | c.890G>A | p.Ser297Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/12 | 905/3970 | 890/1866 | 297/621 | chr19 | 18451628 | |||
| chr19:18461595 | C | T | 1 | a0003 | 2 | HG02004.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.727G>A | p.Asp243Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 742/3970 | 727/1866 | 243/621 | chr19 | 18461595 | |||
| chr19:18461669 | C | T | 1 | a0006 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.653G>A | p.Arg218Gln | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 668/3970 | 653/1866 | 218/621 | chr19 | 18461669 | |||
| chr19:18465511 | C | T | 1 | a0004 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.370G>A | p.Asp124Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/12 | 385/3970 | 370/1866 | 124/621 | chr19 | 18465511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18446405 | G | A | 1 | a0001c0003 | 3 | HG02965.hp2 HG03098.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1608C>T | p.Tyr536Tyr | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/12 | 1623/3970 | 1608/1866 | 536/621 | chr19 | 18446405 | |||
| chr19:18446771 | C | T | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1509G>A | p.Thr503Thr | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/12 | 1524/3970 | 1509/1866 | 503/621 | chr19 | 18446771 | |||
| chr19:18446807 | G | A | 1 | a0001c0012 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1473C>T | p.Asn491Asn | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/12 | 1488/3970 | 1473/1866 | 491/621 | chr19 | 18446807 | |||
| chr19:18450499 | G | A | 1 | a0001c0013 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1443C>T | p.Pro481Pro | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1458/3970 | 1443/1866 | 481/621 | chr19 | 18450499 | |||
| chr19:18450610 | C | T | 2 | a0001c0004 a0001c0005 |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1332G>A | p.Ser444Ser | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1347/3970 | 1332/1866 | 444/621 | chr19 | 18450610 | |||
| chr19:18450663 | G | A | 2 | a0001c0004 a0001c0005 |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.1279C>T | p.Leu427Leu | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/12 | 1294/3970 | 1279/1866 | 427/621 | chr19 | 18450663 | |||
| chr19:18451582 | G | A | 1 | a0001c0007 | 2 | NA18522.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.936C>T | p.Gly312Gly | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/12 | 951/3970 | 936/1866 | 312/621 | chr19 | 18451582 | |||
| chr19:18461806 | C | A | 1 | a0001c0005 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.516G>T | p.Ala172Ala | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/12 | 531/3970 | 516/1866 | 172/621 | chr19 | 18461806 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18442676 | A | G | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 2076 | chr19 | 18442676 | ||||||
| chr19:18442770 | CAGAT | C | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(19): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1978_*1981delATCT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1978 | chr19 | 18442770 | ||||||
| chr19:18442875 | GA | G | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(18): Show |
148 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1876delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1876 | chr19 | 18442875 | ||||||
| chr19:18443394 | G | GAC | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(19): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1356_*1357dupGT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1357 | chr19 | 18443394 | ||||||
| chr19:18443489 | T | C | 1 | a0001c0001t0015 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1263 | chr19 | 18443489 | ||||||
| chr19:18443493 | C | T | 1 | a0001c0001t0012 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1259 | chr19 | 18443493 | ||||||
| chr19:18443567 | C | T | 2 | a0001c0004t0006 a0001c0005t0007 |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1185G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1185 | chr19 | 18443567 | ||||||
| chr19:18443751 | C | G | 1 | a0002c0002t0008 | 2 | HG01346.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1001G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 1001 | chr19 | 18443751 | ||||||
| chr19:18443795 | T | C | 1 | a0002c0002t0013 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*957A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 957 | chr19 | 18443795 | ||||||
| chr19:18443804 | T | C | 2 | a0002c0002t0005 a0002c0002t0019 |
5 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 948 | chr19 | 18443804 | ||||||
| chr19:18443855 | C | T | 2 | a0001c0001t0004 a0001c0001t0011 |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*897G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 897 | chr19 | 18443855 | ||||||
| chr19:18443975 | C | G | 1 | a0001c0005t0007 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*777G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 777 | chr19 | 18443975 | ||||||
| chr19:18443997 | C | A | 1 | a0001c0001t0014 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*755G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 755 | chr19 | 18443997 | ||||||
| chr19:18444162 | A | G | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(19): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*590T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 590 | chr19 | 18444162 | ||||||
| chr19:18444178 | G | A | 1 | a0001c0007t0009 | 2 | NA18522.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*574C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 574 | chr19 | 18444178 | ||||||
| chr19:18444195 | C | T | 1 | a0001c0001t0003 | 7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 557 | chr19 | 18444195 | ||||||
| chr19:18444234 | C | A | 1 | a0001c0001t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*518G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 518 | chr19 | 18444234 | ||||||
| chr19:18444238 | G | A | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 514 | chr19 | 18444238 | ||||||
| chr19:18444303 | G | A | 1 | a0001c0001t0018 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 449 | chr19 | 18444303 | ||||||
| chr19:18444463 | G | A | 1 | a0001c0005t0007 | 3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*289C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 289 | chr19 | 18444463 | ||||||
| chr19:18444639 | G | A | 1 | a0002c0002t0019 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 113 | chr19 | 18444639 | ||||||
| chr19:18444717 | C | T | 1 | a0001c0012t0010 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*35G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 12/12 | 35 | chr19 | 18444717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:18444947 | C | T | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1750-79G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 11/11 | chr19 | 18444947 | |||||||
| chr19:18445535 | CGTGGGGG others(12): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1705-286_1705-268d others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445535 | |||||||
| chr19:18445607 | A | C | 42 | a0001c0001t0002g0076 a0002c0002t0001g0015 a0002c0002t0001g0017 others(39): Show |
42 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1705-339T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445607 | |||||||
| chr19:18445939 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(119): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1704+370A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18445939 | |||||||
| chr19:18446031 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1704+278A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18446031 | |||||||
| chr19:18446225 | A | AGCAGGCC others(5): Show |
123 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(120): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1704+83_1704+84ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 10/11 | chr19 | 18446225 | |||||||
| chr19:18446502 | A | G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0050 a0001c0001t0002g0108 others(1): Show |
5 | NA18975.hp1 NA19060.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-22T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/11 | chr19 | 18446502 | |||||||
| chr19:18446561 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533-81C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 9/11 | chr19 | 18446561 | |||||||
| chr19:18446847 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(77): Show |
81 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1466-33G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18446847 | |||||||
| chr19:18446863 | C | T | 40 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(37): Show |
40 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1466-49G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18446863 | |||||||
| chr19:18447014 | G | A | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1466-200C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447014 | |||||||
| chr19:18447059 | C | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466-245G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447059 | |||||||
| chr19:18447375 | T | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1466-561A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447375 | |||||||
| chr19:18447528 | G | A | 2 | a0001c0004t0006g0170 a0001c0004t0006g0172 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1466-714C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447528 | |||||||
| chr19:18447615 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1466-801T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447615 | |||||||
| chr19:18447707 | G | A | 2 | a0002c0002t0008g0116 a0002c0002t0008g0118 |
2 | HG01346.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1466-893C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447707 | |||||||
| chr19:18447785 | CT | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0179 others(6): Show |
9 | HG01069.hp1 HG01515.hp2 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.1466-972delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18447785 | |||||||
| chr19:18448009 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1466-1195G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448009 | |||||||
| chr19:18448066 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(120): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1466-1252T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448066 | |||||||
| chr19:18448087 | AT | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0169 a0001c0001t0001g0184 others(15): Show |
18 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1466-1274delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448087 | |||||||
| chr19:18448133 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1466-1319G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448133 | |||||||
| chr19:18448257 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1466-1443G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448257 | |||||||
| chr19:18448281 | AG | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(20): Show |
23 | HG00280.hp2 HG01081.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1466-1468delC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448281 | |||||||
| chr19:18448287 | C | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0222 |
2 | HG01952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1466-1473G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448287 | |||||||
| chr19:18448489 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1466-1675G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448489 | |||||||
| chr19:18448538 | C | T | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1466-1724G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448538 | |||||||
| chr19:18448600 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1466-1786C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448600 | |||||||
| chr19:18448703 | CA | C | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1465+1773delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448703 | |||||||
| chr19:18448844 | C | T | 1 | a0001c0001t0003g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1465+1633G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448844 | |||||||
| chr19:18448847 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(120): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1465+1630C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448847 | |||||||
| chr19:18448853 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1465+1624C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18448853 | |||||||
| chr19:18449006 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1465+1471G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449006 | |||||||
| chr19:18449039 | T | G | 1 | a0005c0011t0001g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1465+1438A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449039 | |||||||
| chr19:18449472 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1465+1005A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449472 | |||||||
| chr19:18449491 | A | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1465+986T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449491 | |||||||
| chr19:18449753 | G | A | 4 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
4 | HG00642.hp1 HG01515.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465+724C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449753 | |||||||
| chr19:18449822 | C | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465+655G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449822 | |||||||
| chr19:18449892 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0222 |
2 | HG01952.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1465+585C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449892 | |||||||
| chr19:18449974 | C | CG | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1465+502dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 8/11 | chr19 | 18449974 | |||||||
| chr19:18450991 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.967-16C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18450991 | |||||||
| chr19:18451182 | G | A | 6 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(3): Show |
6 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.967-207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451182 | |||||||
| chr19:18451292 | G | C | 6 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+260C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451292 | |||||||
| chr19:18451303 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.966+249T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451303 | |||||||
| chr19:18451340 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.966+212C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451340 | |||||||
| chr19:18451429 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.966+123C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451429 | |||||||
| chr19:18451449 | T | A | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.966+103A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451449 | |||||||
| chr19:18451498 | C | T | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.966+54G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451498 | |||||||
| chr19:18451517 | G | A | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.966+35C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451517 | |||||||
| chr19:18451535 | A | C | 9 | a0001c0001t0002g0035 a0001c0001t0002g0088 a0001c0001t0002g0089 others(6): Show |
9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.966+17T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 7/11 | chr19 | 18451535 | |||||||
| chr19:18451814 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-166G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451814 | |||||||
| chr19:18451823 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-175C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451823 | |||||||
| chr19:18451937 | C | T | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.870-289G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18451937 | |||||||
| chr19:18452141 | T | A | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-493A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452141 | |||||||
| chr19:18452143 | C | A | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-495G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452143 | |||||||
| chr19:18452151 | T | A | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.870-503A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452151 | |||||||
| chr19:18452195 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-547G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452195 | |||||||
| chr19:18452249 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.870-601G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452249 | |||||||
| chr19:18452278 | GCGC | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0158 a0001c0001t0001g0160 others(8): Show |
11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-633_870-631del others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452278 | |||||||
| chr19:18452286 | C | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0158 a0001c0001t0001g0160 others(8): Show |
11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.870-638G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452286 | |||||||
| chr19:18452600 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-952G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452600 | |||||||
| chr19:18452726 | G | A | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.870-1078C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452726 | |||||||
| chr19:18452874 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.870-1226G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452874 | |||||||
| chr19:18452891 | C | G | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.870-1243G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452891 | |||||||
| chr19:18452904 | G | A | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.870-1256C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18452904 | |||||||
| chr19:18453070 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-1422C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453070 | |||||||
| chr19:18453160 | A | C | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.870-1512T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453160 | |||||||
| chr19:18453225 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.870-1577C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453225 | |||||||
| chr19:18453563 | G | A | 6 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1915C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453563 | |||||||
| chr19:18453573 | A | G | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-1925T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453573 | |||||||
| chr19:18453590 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-1942C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453590 | |||||||
| chr19:18453608 | C | T | 6 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.870-1960G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453608 | |||||||
| chr19:18453895 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.870-2247T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18453895 | |||||||
| chr19:18454097 | G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.870-2449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454097 | |||||||
| chr19:18454229 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.870-2581T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454229 | |||||||
| chr19:18454412 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.870-2764A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454412 | |||||||
| chr19:18454493 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.870-2845C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454493 | |||||||
| chr19:18454510 | G | T | 7 | a0001c0001t0002g0049 a0001c0001t0002g0062 a0001c0001t0002g0066 others(4): Show |
7 | HG00408.hp1 HG01975.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-2862C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454510 | |||||||
| chr19:18454698 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.870-3050C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454698 | |||||||
| chr19:18454747 | A | G | 1 | a0001c0010t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.870-3099T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454747 | |||||||
| chr19:18454784 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.870-3136A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454784 | |||||||
| chr19:18454840 | C | CA | 5 | a0001c0001t0001g0156 a0001c0001t0002g0049 a0001c0001t0002g0051 others(2): Show |
5 | HG02055.hp2 HG02056.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.870-3193dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAA | 9 | a0001c0001t0001g0224 a0002c0002t0001g0014 a0002c0002t0001g0015 others(6): Show |
9 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.870-3195_870-3193d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAA | 11 | a0001c0001t0001g0178 a0001c0001t0001g0220 a0001c0001t0001g0223 others(8): Show |
11 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.870-3196_870-3193d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAA | 22 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0112 others(19): Show |
22 | HG00733.hp2 HG01081.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.870-3197_870-3193d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.870-3202_870-3193d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0180 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG01255.hp1 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.870-3203_870-3193d others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.870-3204_870-3193d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0227 others(1): Show |
4 | HG01109.hp1 HG01943.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3205_870-3193d others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.870-3206_870-3193d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0214 a0001c0013t0001g0207 |
2 | HG02738.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.870-3207_870-3193d others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0209 a0003c0006t0001g0211 |
2 | HG01433.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.870-3208_870-3193d others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.870-3209_870-3193d others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0183 a0001c0001t0001g0204 |
2 | HG02132.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.870-3210_870-3193d others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0202 a0001c0001t0004g0153 |
2 | HG00408.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0004g0152 |
3 | HG01123.hp1 HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(14): Show |
3 | a0001c0001t0001g0218 a0001c0001t0004g0151 a0001c0001t0004g0154 |
3 | HG02145.hp1 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(23): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0212 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0221 a0001c0001t0001g0237 |
3 | HG02300.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(18): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0200 |
2 | HG00280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(27): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(29): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(21): Show |
4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0193 others(1): Show |
4 | HG01167.hp1 HG01952.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(24): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0210 |
2 | HG01928.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(33): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(25): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0217 |
2 | HG01074.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(34): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0192 a0001c0001t0012g0228 |
2 | HG00642.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.870-3193_870-3192i others(35): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(36): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0018g0196 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(37): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(30): Show |
4 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0231 others(1): Show |
4 | HG00735.hp2 HG01261.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-3193_870-3192i others(39): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(31): Show |
1 | a0003c0006t0001g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(40): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(33): Show |
1 | a0001c0001t0001g0235 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.870-3193_870-3192i others(42): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0219 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(47): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | C | CAAAAAAA others(53): Show |
1 | a0001c0001t0001g0203 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.870-3193_870-3192i others(62): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454840 | CA | C | 13 | a0001c0001t0001g0144 a0001c0001t0002g0035 a0001c0001t0002g0053 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.870-3193delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454840 | |||||||
| chr19:18454938 | G | C | 1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.869+3267C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454938 | |||||||
| chr19:18454998 | G | A | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.869+3207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18454998 | |||||||
| chr19:18455065 | G | A | 4 | a0002c0002t0005g0119 a0002c0002t0005g0120 a0002c0002t0005g0121 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.869+3140C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455065 | |||||||
| chr19:18455122 | T | C | 6 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+3083A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455122 | |||||||
| chr19:18455141 | CA | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
140 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.869+3063delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455141 | |||||||
| chr19:18455153 | A | G | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869+3052T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455153 | |||||||
| chr19:18455226 | ATCACGCC others(599): Show |
A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0042 |
2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.869+2373_869+2978d others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455226 | |||||||
| chr19:18455359 | C | T | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.869+2846G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455359 | |||||||
| chr19:18455537 | G | A | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.869+2668C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455537 | |||||||
| chr19:18455585 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.869+2620A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455585 | |||||||
| chr19:18455826 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.869+2379G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455826 | |||||||
| chr19:18455827 | G | A | 57 | a0001c0001t0001g0144 a0001c0001t0003g0020 a0001c0001t0003g0021 others(54): Show |
57 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.869+2378C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455827 | |||||||
| chr19:18455994 | T | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
151 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.869+2211A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18455994 | |||||||
| chr19:18456097 | CA | C | 6 | a0001c0001t0001g0149 a0001c0001t0003g0021 a0001c0004t0006g0170 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+2107delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456097 | |||||||
| chr19:18456180 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.869+2025C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456180 | |||||||
| chr19:18456183 | G | A | 6 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.869+2022C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456183 | |||||||
| chr19:18456229 | C | T | 59 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(56): Show |
60 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.869+1976G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456229 | |||||||
| chr19:18456379 | A | G | 45 | a0001c0001t0001g0216 a0001c0001t0004g0150 a0002c0002t0001g0014 others(42): Show |
45 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.869+1826T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456379 | |||||||
| chr19:18456745 | C | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.869+1460G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456745 | |||||||
| chr19:18456763 | CAGCT | C | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+1438_869+1441d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456763 | |||||||
| chr19:18456772 | T | C | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+1433A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456772 | |||||||
| chr19:18456946 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.869+1259A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456946 | |||||||
| chr19:18456961 | G | GA | 15 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0002g0043 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.869+1243dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456961 | |||||||
| chr19:18456961 | GA | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0001t0001g0177 others(66): Show |
70 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.869+1243delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18456961 | |||||||
| chr19:18457091 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.869+1114G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457091 | |||||||
| chr19:18457225 | G | A | 2 | a0001c0001t0001g0206 a0001c0013t0001g0207 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.869+980C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457225 | |||||||
| chr19:18457370 | C | A | 1 | a0003c0006t0001g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.869+835G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457370 | |||||||
| chr19:18457753 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.869+452G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457753 | |||||||
| chr19:18457779 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.869+426C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457779 | |||||||
| chr19:18457788 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.869+417C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457788 | |||||||
| chr19:18457806 | C | CT | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.869+398dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457806 | |||||||
| chr19:18457984 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.869+221G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457984 | |||||||
| chr19:18457985 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.869+220C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18457985 | |||||||
| chr19:18458141 | C | G | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.869+64G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 6/11 | chr19 | 18458141 | |||||||
| chr19:18458343 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.745-14G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458343 | |||||||
| chr19:18458402 | T | C | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.745-73A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458402 | |||||||
| chr19:18458485 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.745-156C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458485 | |||||||
| chr19:18458601 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.745-272C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458601 | |||||||
| chr19:18458624 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.745-295T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458624 | |||||||
| chr19:18458672 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0073 |
2 | HG01257.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.745-343C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458672 | |||||||
| chr19:18458682 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.745-353G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458682 | |||||||
| chr19:18458800 | A | T | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-471T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458800 | |||||||
| chr19:18458943 | C | CAGTG | 10 | a0001c0001t0002g0033 a0001c0001t0002g0051 a0001c0001t0002g0052 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.745-618_745-615dup others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18458943 | |||||||
| chr19:18459023 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.745-694C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459023 | |||||||
| chr19:18459100 | G | A | 3 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 |
3 | HG00642.hp1 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.745-771C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459100 | |||||||
| chr19:18459144 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.745-815C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459144 | |||||||
| chr19:18459147 | G | A | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.745-818C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459147 | |||||||
| chr19:18459225 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.745-896C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459225 | |||||||
| chr19:18459258 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.745-929C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459258 | |||||||
| chr19:18459521 | AT | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0193 a0001c0001t0001g0222 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.745-1193delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459521 | |||||||
| chr19:18459564 | G | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1235C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459564 | |||||||
| chr19:18459565 | GCT | G | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1238_745-1237d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459565 | |||||||
| chr19:18459566 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.745-1237G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459566 | |||||||
| chr19:18459569 | G | T | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1240C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459569 | |||||||
| chr19:18459613 | G | C | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1284C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459613 | |||||||
| chr19:18459669 | G | C | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-1340C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459669 | |||||||
| chr19:18459716 | T | TG | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.745-1388dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459716 | |||||||
| chr19:18459777 | C | T | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.745-1448G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459777 | |||||||
| chr19:18459809 | A | G | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.745-1480T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459809 | |||||||
| chr19:18459822 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.745-1493C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459822 | |||||||
| chr19:18459847 | T | C | 1 | a0003c0006t0001g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.745-1518A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18459847 | |||||||
| chr19:18460172 | C | G | 2 | a0002c0002t0001g0112 a0002c0002t0013g0113 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.744+1406G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460172 | |||||||
| chr19:18460179 | T | G | 1 | a0001c0001t0002g0066 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.744+1399A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460179 | |||||||
| chr19:18460187 | A | AG | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1390_744+1391i others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460187 | |||||||
| chr19:18460190 | T | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1388A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460190 | |||||||
| chr19:18460191 | C | CAG | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1386_744+1387i others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460191 | |||||||
| chr19:18460293 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1285C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460293 | |||||||
| chr19:18460331 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
143 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.744+1247T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460331 | |||||||
| chr19:18460340 | G | A | 43 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(40): Show |
43 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.744+1238C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460340 | |||||||
| chr19:18460357 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.744+1221C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460357 | |||||||
| chr19:18460417 | T | A | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.744+1161A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460417 | |||||||
| chr19:18460590 | C | A | 1 | a0002c0002t0001g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.744+988G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460590 | |||||||
| chr19:18460834 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+744C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460834 | |||||||
| chr19:18460923 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.744+655G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460923 | |||||||
| chr19:18460926 | A | T | 1 | a0002c0002t0019g0131 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.744+652T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18460926 | |||||||
| chr19:18461022 | G | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+556C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461022 | |||||||
| chr19:18461058 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.744+520G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461058 | |||||||
| chr19:18461168 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.744+410C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461168 | |||||||
| chr19:18461231 | C | T | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+347G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461231 | |||||||
| chr19:18461267 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0158 a0001c0001t0001g0160 others(8): Show |
11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+311G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461267 | |||||||
| chr19:18461291 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.744+287G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461291 | |||||||
| chr19:18461403 | T | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.744+175A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461403 | |||||||
| chr19:18461482 | G | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0158 a0001c0001t0001g0160 others(8): Show |
11 | HG01081.hp1 HG02886.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+96C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461482 | |||||||
| chr19:18461545 | C | T | 3 | a0001c0001t0002g0028 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG01243.hp1 HG01496.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.744+33G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 5/11 | chr19 | 18461545 | |||||||
| chr19:18461950 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.470-98T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18461950 | |||||||
| chr19:18462024 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
141 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.470-172G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462024 | |||||||
| chr19:18462179 | A | AGT | 23 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(20): Show |
23 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.470-329_470-328dup others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | |||||||
| chr19:18462179 | A | AGTGT | 10 | a0001c0001t0001g0144 a0001c0001t0002g0036 a0001c0001t0002g0037 others(7): Show |
10 | HG01928.hp1 HG02809.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-331_470-328dup others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | |||||||
| chr19:18462179 | A | AGTGTGT | 4 | a0001c0001t0002g0062 a0001c0001t0002g0087 a0001c0001t0015g0065 others(1): Show |
4 | HG00408.hp1 HG00741.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-333_470-328dup others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462179 | |||||||
| chr19:18462204 | GTGTGTGT others(11): Show |
G | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-370_470-353del others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462204 | |||||||
| chr19:18462210 | GTGTGTGT others(5): Show |
G | 5 | a0001c0001t0001g0179 a0001c0001t0001g0190 a0001c0001t0001g0198 others(2): Show |
5 | HG01515.hp2 HG01884.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-370_470-359del others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462210 | |||||||
| chr19:18462212 | GTGTGTGT others(3): Show |
G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(7): Show |
11 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.470-370_470-361del others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462212 | |||||||
| chr19:18462214 | GTGTGTGT others(1): Show |
G | 14 | a0001c0001t0001g0156 a0001c0001t0001g0214 a0001c0001t0001g0216 others(11): Show |
14 | HG01884.hp2 HG02055.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.470-370_470-363del others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462214 | |||||||
| chr19:18462216 | GTGTGTA | G | 37 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0001c0001t0001g0180 others(34): Show |
37 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.470-370_470-365del others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462216 | |||||||
| chr19:18462218 | GTGTA | G | 42 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0155 others(39): Show |
42 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.470-370_470-367del others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462218 | |||||||
| chr19:18462220 | GTA | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(21): Show |
24 | HG01109.hp1 HG01433.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.470-370_470-369del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462220 | |||||||
| chr19:18462222 | A | G | 11 | a0001c0001t0001g0144 a0001c0001t0001g0166 a0001c0001t0001g0202 others(8): Show |
11 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-370T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462222 | |||||||
| chr19:18462232 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.470-380G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462232 | |||||||
| chr19:18462253 | A | G | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
235 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.470-401T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462253 | |||||||
| chr19:18462334 | G | GGT | 20 | a0002c0002t0001g0110 a0002c0002t0001g0112 a0002c0002t0001g0114 others(17): Show |
20 | HG01081.hp2 HG01258.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-483_470-482ins others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | |||||||
| chr19:18462334 | G | GGTGT | 8 | a0001c0001t0011g0115 a0002c0002t0001g0109 a0002c0002t0001g0129 others(5): Show |
8 | HG00323.hp2 HG01884.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-483_470-482ins others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | |||||||
| chr19:18462334 | G | GGTGTGTG others(3): Show |
2 | a0002c0002t0001g0140 a0002c0002t0001g0142 |
2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.470-483_470-482ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | |||||||
| chr19:18462334 | G | GGTGTGTG others(7): Show |
1 | a0002c0002t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.470-483_470-482ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | |||||||
| chr19:18462334 | GCT | G | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-484_470-483del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462334 | |||||||
| chr19:18462335 | C | CTGTGTG | 11 | a0001c0001t0001g0160 a0001c0001t0001g0177 a0001c0001t0001g0178 others(8): Show |
11 | HG00408.hp2 HG02886.hp2 HG03540.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-489_470-484dup others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462335 | C | CTGTGTGT others(1): Show |
16 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(13): Show |
16 | HG00280.hp2 HG00642.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.470-491_470-484dup others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462335 | C | CTGTGTGT others(3): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0190 a0001c0001t0001g0212 others(4): Show |
7 | HG02451.hp1 HG02965.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-493_470-484dup others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462335 | C | CTGTGTGT others(5): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0198 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.470-495_470-484dup others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462335 | C | G | 39 | a0001c0001t0011g0115 a0002c0002t0001g0109 a0002c0002t0001g0110 others(36): Show |
39 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.470-483G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462335 | CTG | C | 14 | a0001c0001t0002g0007 a0001c0001t0002g0019 a0001c0001t0002g0027 others(11): Show |
14 | HG01361.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.470-485_470-484del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462335 | |||||||
| chr19:18462337 | G | C | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-485C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462337 | |||||||
| chr19:18462352 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-500A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462352 | |||||||
| chr19:18462353 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0001g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-514_470-502del others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462353 | |||||||
| chr19:18462362 | T | G | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-510A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462362 | |||||||
| chr19:18462364 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.470-513_470-512ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462364 | |||||||
| chr19:18462365 | T | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
103 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.470-513A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462365 | |||||||
| chr19:18462366 | T | C | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-514A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0206 |
2 | HG01891.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.470-514A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGGG others(1): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0156 a0001c0001t0001g0222 |
3 | HG01346.hp1 HG02055.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGGG others(3): Show |
1 | a0001c0001t0001g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGGG others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(3): Show |
5 | a0001c0001t0001g0147 a0001c0001t0001g0167 a0001c0001t0001g0210 others(2): Show |
5 | HG01516.hp1 HG01928.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0001g0219 a0001c0003t0001g0163 |
2 | HG03098.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(6): Show |
2 | a0001c0001t0001g0185 a0001c0001t0001g0229 |
2 | HG01261.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(5): Show |
6 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0001g0188 others(3): Show |
6 | HG00735.hp2 HG01069.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(6): Show |
4 | a0001c0001t0001g0003 a0001c0001t0004g0151 a0001c0001t0004g0154 others(1): Show |
4 | HG01071.hp1 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-515_470-514ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0001g0194 a0001c0001t0004g0152 |
2 | HG01167.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.470-515_470-514ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0001g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.470-515_470-514ins others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0017g0189 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0001g0232 a0001c0001t0004g0153 a0003c0006t0001g0211 |
3 | HG01099.hp2 HG01169.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.470-515_470-514ins others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0215 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462366 | T | TGTGTGTG others(21): Show |
1 | a0002c0002t0001g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.470-515_470-514ins others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462366 | |||||||
| chr19:18462367 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.470-515C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GT | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-516_470-515ins others(1): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GTGTGTGG others(2): Show |
6 | a0001c0001t0001g0164 a0001c0001t0001g0169 a0001c0001t0001g0181 others(3): Show |
6 | HG01167.hp1 HG01943.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-516_470-515ins others(9): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GTGTGTGT others(4): Show |
4 | a0001c0001t0001g0192 a0001c0001t0001g0209 a0001c0001t0001g0214 others(1): Show |
4 | HG01433.hp2 HG02293.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-516_470-515ins others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0014g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.470-516_470-515ins others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GTGTGTGT others(6): Show |
3 | a0001c0001t0001g0158 a0001c0001t0001g0195 a0007c0014t0001g0013 |
3 | HG01081.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.470-516_470-515ins others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462367 | G | GTGTGTGT others(10): Show |
1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.470-516_470-515ins others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462367 | |||||||
| chr19:18462368 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.470-516C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462368 | |||||||
| chr19:18462368 | G | T | 8 | a0001c0001t0001g0144 a0001c0001t0001g0180 a0001c0001t0001g0184 others(5): Show |
8 | HG01074.hp2 HG01255.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-516C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462368 | |||||||
| chr19:18462369 | G | T | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-517C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462369 | |||||||
| chr19:18462370 | C | CG | 18 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(15): Show |
18 | HG01891.hp1 HG02004.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.470-519dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | |||||||
| chr19:18462370 | C | CGG | 33 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0168 others(30): Show |
33 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.470-520_470-519dup others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | |||||||
| chr19:18462370 | C | CGGGGGGG others(3): Show |
1 | a0002c0002t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.470-519_470-518ins others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | |||||||
| chr19:18462370 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(51): Show |
55 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.470-518G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | |||||||
| chr19:18462370 | C | T | 11 | a0001c0001t0001g0144 a0001c0001t0001g0180 a0001c0001t0001g0184 others(8): Show |
11 | HG01074.hp2 HG01255.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-518G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462370 | |||||||
| chr19:18462371 | G | GTTT | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.470-520_470-519ins others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462371 | |||||||
| chr19:18462371 | G | T | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.470-519C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462371 | |||||||
| chr19:18462372 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0235 |
2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-520C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462372 | |||||||
| chr19:18462373 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0184 |
2 | HG01074.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.470-521C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462373 | |||||||
| chr19:18462374 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0235 |
2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-522C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462374 | |||||||
| chr19:18462375 | G | C | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-523C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462375 | |||||||
| chr19:18462376 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.470-524C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462376 | |||||||
| chr19:18462377 | C | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
145 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.470-525G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462377 | |||||||
| chr19:18462378 | G | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0235 |
2 | NA18951.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.470-526C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462378 | |||||||
| chr19:18462379 | G | T | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.470-527C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462379 | |||||||
| chr19:18462385 | G | GGGGGGGG others(7): Show |
1 | a0002c0002t0001g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.470-534_470-533ins others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462385 | |||||||
| chr19:18462391 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-539A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462391 | |||||||
| chr19:18462451 | A | G | 1 | a0001c0010t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.470-599T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462451 | |||||||
| chr19:18462865 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.470-1013T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18462865 | |||||||
| chr19:18463217 | G | C | 9 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(6): Show |
9 | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.470-1365C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463217 | |||||||
| chr19:18463268 | G | A | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-1416C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463268 | |||||||
| chr19:18463325 | C | CT | 15 | a0001c0001t0001g0177 a0001c0001t0001g0221 a0001c0001t0002g0033 others(12): Show |
15 | HG00642.hp1 HG01109.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.470-1474dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | |||||||
| chr19:18463325 | CT | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(88): Show |
92 | HG00280.hp2 HG00408.hp2 HG01069.hp1 others(89): Show |
intron_variant | MODIFIER | c.470-1474delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | |||||||
| chr19:18463325 | CTT | C | 42 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0204 others(39): Show |
42 | HG00323.hp2 HG00733.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.470-1475_470-1474d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | |||||||
| chr19:18463325 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.470-1487_470-1474d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463325 | |||||||
| chr19:18463425 | T | C | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.470-1573A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463425 | |||||||
| chr19:18463444 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.470-1592G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463444 | |||||||
| chr19:18463731 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.469+1681G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463731 | |||||||
| chr19:18463749 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+1663A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463749 | |||||||
| chr19:18463775 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.469+1637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463775 | |||||||
| chr19:18463968 | A | G | 1 | a0001c0001t0002g0105 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.469+1444T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463968 | |||||||
| chr19:18463985 | C | CA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
97 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.469+1426dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463985 | |||||||
| chr19:18463998 | C | A | 1 | a0002c0002t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.469+1414G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18463998 | |||||||
| chr19:18464297 | T | G | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+1115A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464297 | |||||||
| chr19:18464375 | A | G | 1 | a0002c0002t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.469+1037T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464375 | |||||||
| chr19:18464383 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0061 |
4 | HG01123.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+1029T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464383 | |||||||
| chr19:18464490 | TACA | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.469+919_469+921del others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464490 | |||||||
| chr19:18464640 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.469+772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464640 | |||||||
| chr19:18464719 | C | T | 3 | a0001c0001t0002g0047 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG00735.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.469+693G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464719 | |||||||
| chr19:18464770 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.469+642A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464770 | |||||||
| chr19:18464889 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0096 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.469+523C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464889 | |||||||
| chr19:18464979 | G | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+433C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464979 | |||||||
| chr19:18464998 | G | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+414C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18464998 | |||||||
| chr19:18465053 | G | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+359C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465053 | |||||||
| chr19:18465339 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.469+73C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465339 | |||||||
| chr19:18465344 | G | A | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.469+68C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 4/11 | chr19 | 18465344 | |||||||
| chr19:18465674 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.306-99A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465674 | |||||||
| chr19:18465704 | T | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+93A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465704 | |||||||
| chr19:18465791 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.305+6G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 3/11 | chr19 | 18465791 | |||||||
| chr19:18465957 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.184-39C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18465957 | |||||||
| chr19:18466072 | C | T | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-154G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466072 | |||||||
| chr19:18466118 | G | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-200C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466118 | |||||||
| chr19:18466123 | AGGCACC | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-211_184-206del others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466123 | |||||||
| chr19:18466130 | T | G | 1 | a0001c0001t0002g0066 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.184-212A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466130 | |||||||
| chr19:18466475 | C | T | 6 | a0001c0001t0011g0115 a0002c0002t0005g0119 a0002c0002t0005g0120 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-557G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466475 | |||||||
| chr19:18466514 | T | C | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-596A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466514 | |||||||
| chr19:18466588 | C | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.184-670G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466588 | |||||||
| chr19:18466635 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.184-717C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18466635 | |||||||
| chr19:18467063 | G | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1145C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467063 | |||||||
| chr19:18467272 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.184-1354G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467272 | |||||||
| chr19:18467308 | C | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0184 |
2 | HG01074.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.184-1390G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467308 | |||||||
| chr19:18467368 | G | A | 41 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(38): Show |
41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-1450C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467368 | |||||||
| chr19:18467552 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.184-1634G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467552 | |||||||
| chr19:18467631 | C | CCA | 3 | a0001c0001t0002g0054 a0001c0001t0002g0083 a0001c0001t0002g0087 |
3 | HG00741.hp1 HG00741.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.184-1715_184-1714d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | C | CCACA | 4 | a0001c0001t0002g0033 a0001c0001t0002g0051 a0001c0001t0002g0056 others(1): Show |
4 | HG01069.hp2 HG04115.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1717_184-1714d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | C | CCACACA | 4 | a0001c0001t0002g0052 a0001c0001t0002g0055 a0001c0001t0002g0058 others(1): Show |
4 | HG00639.hp2 HG01074.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1719_184-1714d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | C | CCACACAC others(3): Show |
1 | a0001c0001t0002g0053 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.184-1723_184-1714d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACA | C | 15 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0046 others(12): Show |
15 | HG00642.hp1 HG00738.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.184-1717_184-1714d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACA | C | 31 | a0001c0001t0002g0019 a0001c0001t0002g0026 a0001c0001t0002g0027 others(28): Show |
31 | HG00639.hp1 HG00733.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.184-1719_184-1714d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(1): Show |
C | 6 | a0001c0001t0001g0149 a0001c0001t0004g0151 a0001c0001t0004g0152 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1721_184-1714d others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(3): Show |
C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.184-1723_184-1714d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(5): Show |
C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(29): Show |
32 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.184-1725_184-1714d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(7): Show |
C | 9 | a0001c0001t0001g0144 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG01123.hp1 HG02004.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-1727_184-1714d others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(9): Show |
C | 41 | a0001c0001t0002g0007 a0001c0001t0011g0115 a0002c0002t0001g0014 others(38): Show |
41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-1729_184-1714d others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(11): Show |
C | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184-1731_184-1714d others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467631 | CCACACAC others(13): Show |
C | 1 | a0002c0002t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-1733_184-1714d others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467631 | |||||||
| chr19:18467674 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.184-1756T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467674 | |||||||
| chr19:18467701 | CCACA | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0048 others(1): Show |
4 | HG00738.hp1 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1787_184-1784d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467701 | |||||||
| chr19:18467732 | CCACA | C | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.184-1818_184-1815d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467732 | |||||||
| chr19:18467734 | A | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0233 others(1): Show |
4 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1816T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467734 | |||||||
| chr19:18467762 | C | T | 1 | a0001c0001t0018g0196 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.184-1844G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467762 | |||||||
| chr19:18467807 | A | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1889T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467807 | |||||||
| chr19:18467844 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.184-1926A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467844 | |||||||
| chr19:18467879 | A | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
98 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.184-1961T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467879 | |||||||
| chr19:18467941 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.184-2023G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18467941 | |||||||
| chr19:18468027 | A | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0030 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.184-2109T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468027 | |||||||
| chr19:18468087 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.184-2169T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468087 | |||||||
| chr19:18468102 | C | A | 1 | a0002c0002t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.184-2184G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468102 | |||||||
| chr19:18468174 | C | T | 41 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(38): Show |
41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.184-2256G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468174 | |||||||
| chr19:18468214 | CACAA | C | 12 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(9): Show |
12 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.184-2300_184-2297d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468214 | |||||||
| chr19:18468219 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2301T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468219 | |||||||
| chr19:18468221 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2303T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468221 | |||||||
| chr19:18468227 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.184-2309A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | |||||||
| chr19:18468227 | T | TAC | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
110 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(107): Show |
intron_variant | MODIFIER | c.184-2311_184-2310d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | |||||||
| chr19:18468227 | T | TACAC | 40 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0002c0002t0001g0014 others(37): Show |
40 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.184-2313_184-2310d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468227 | |||||||
| chr19:18468339 | C | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.184-2421G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468339 | |||||||
| chr19:18468698 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.184-2780G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468698 | |||||||
| chr19:18468967 | A | G | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.184-3049T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18468967 | |||||||
| chr19:18469141 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.184-3223C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469141 | |||||||
| chr19:18469329 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.184-3411C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469329 | |||||||
| chr19:18469386 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.183+3449C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469386 | |||||||
| chr19:18469772 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.183+3063A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469772 | |||||||
| chr19:18469818 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.183+3017A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469818 | |||||||
| chr19:18469821 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
9 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+3014G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469821 | |||||||
| chr19:18469988 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.183+2847G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18469988 | |||||||
| chr19:18470143 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+2692G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470143 | |||||||
| chr19:18470204 | C | T | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+2631G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470204 | |||||||
| chr19:18470207 | G | A | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.183+2628C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470207 | |||||||
| chr19:18470417 | T | C | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+2418A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470417 | |||||||
| chr19:18470453 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+2382C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18470453 | |||||||
| chr19:18471024 | A | AGAGC | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+1807_183+1810d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471024 | |||||||
| chr19:18471091 | A | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.183+1744T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471091 | |||||||
| chr19:18471106 | C | T | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.183+1729G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471106 | |||||||
| chr19:18471565 | G | A | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.183+1270C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471565 | |||||||
| chr19:18471986 | G | C | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+849C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18471986 | |||||||
| chr19:18472006 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.183+829C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472006 | |||||||
| chr19:18472279 | A | G | 1 | a0002c0002t0019g0131 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.183+556T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472279 | |||||||
| chr19:18472376 | C | T | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+459G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472376 | |||||||
| chr19:18472433 | T | C | 2 | a0002c0002t0008g0116 a0002c0002t0008g0118 |
2 | HG01346.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.183+402A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472433 | |||||||
| chr19:18472657 | C | T | 2 | a0001c0007t0009g0008 a0001c0007t0009g0009 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.183+178G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472657 | |||||||
| chr19:18472658 | G | A | 5 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+177C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 2/11 | chr19 | 18472658 | |||||||
| chr19:18472886 | T | TA | 28 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0202 others(25): Show |
28 | HG00408.hp2 HG01109.hp1 HG01346.hp2 others(25): Show |
splice_region_variant&intron_variant | LOW | c.136-5dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472886 | |||||||
| chr19:18472886 | TA | T | 21 | a0001c0001t0001g0157 a0001c0001t0001g0169 a0001c0001t0001g0184 others(18): Show |
21 | HG00323.hp1 HG01069.hp1 HG01069.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.136-5delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472886 | |||||||
| chr19:18472986 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.136-104A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18472986 | |||||||
| chr19:18473060 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-178A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473060 | |||||||
| chr19:18473153 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-271C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473153 | |||||||
| chr19:18473421 | C | G | 2 | a0002c0002t0001g0112 a0002c0002t0013g0113 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.136-539G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473421 | |||||||
| chr19:18473494 | C | A | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | HG01175.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.136-612G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473494 | |||||||
| chr19:18473590 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.136-708A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473590 | |||||||
| chr19:18473668 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
100 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.136-786G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473668 | |||||||
| chr19:18473810 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0024 |
2 | HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.136-928A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473810 | |||||||
| chr19:18473893 | A | AC | 4 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0002g0084 others(1): Show |
4 | HG01978.hp2 NA18985.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1012dupG | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473893 | |||||||
| chr19:18473910 | G | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-1028C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473910 | |||||||
| chr19:18473934 | C | T | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1052G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473934 | |||||||
| chr19:18473971 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-1089C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18473971 | |||||||
| chr19:18474184 | CA | C | 4 | a0002c0002t0001g0238 a0002c0002t0001g0239 a0002c0002t0001g0240 others(1): Show |
4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1303delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474184 | |||||||
| chr19:18474197 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-1315C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474197 | |||||||
| chr19:18474297 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-1415C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474297 | |||||||
| chr19:18474349 | C | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-1467G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474349 | |||||||
| chr19:18474349 | C | T | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-1467G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474349 | |||||||
| chr19:18474515 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.136-1633T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474515 | |||||||
| chr19:18474519 | G | A | 24 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0112 others(21): Show |
24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-1637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474519 | |||||||
| chr19:18474546 | A | C | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0230 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-1664T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474546 | |||||||
| chr19:18474572 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0218 |
3 | HG02451.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.136-1690C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474572 | |||||||
| chr19:18474600 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-1718G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474600 | |||||||
| chr19:18474736 | G | A | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-1854C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18474736 | |||||||
| chr19:18475024 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.136-2142G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475024 | |||||||
| chr19:18475072 | T | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2190A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475072 | |||||||
| chr19:18475075 | G | T | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-2193C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475075 | |||||||
| chr19:18475126 | C | G | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2244G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475126 | |||||||
| chr19:18475159 | G | C | 1 | a0003c0006t0001g0211 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.136-2277C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475159 | |||||||
| chr19:18475330 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136-2448C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475330 | |||||||
| chr19:18475355 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-2473G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475355 | |||||||
| chr19:18475403 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-2521C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475403 | |||||||
| chr19:18475489 | C | CT | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.136-2608_136-2607i others(3): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475489 | |||||||
| chr19:18475669 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0198 a0001c0001t0014g0197 |
3 | HG01884.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136-2787A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475669 | |||||||
| chr19:18475709 | T | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-2827A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475709 | |||||||
| chr19:18475791 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0221 |
2 | HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.136-2909C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475791 | |||||||
| chr19:18475949 | G | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-3067C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475949 | |||||||
| chr19:18475981 | C | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-3099G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18475981 | |||||||
| chr19:18476020 | G | A | 3 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 |
3 | HG02735.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.136-3138C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476020 | |||||||
| chr19:18476130 | G | C | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-3248C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476130 | |||||||
| chr19:18476222 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.136-3340C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476222 | |||||||
| chr19:18476347 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-3465G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476347 | |||||||
| chr19:18476362 | G | T | 3 | a0001c0001t0002g0047 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG00735.hp1 HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.136-3480C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476362 | |||||||
| chr19:18476430 | T | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-3548A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476430 | |||||||
| chr19:18476535 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.136-3653C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476535 | |||||||
| chr19:18476882 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.136-4000G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18476882 | |||||||
| chr19:18477052 | G | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0125 |
2 | NA18964.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.136-4170C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477052 | |||||||
| chr19:18477334 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.136-4452C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477334 | |||||||
| chr19:18477334 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-4452C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477334 | |||||||
| chr19:18477484 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.136-4602C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477484 | |||||||
| chr19:18477519 | G | A | 1 | a0003c0006t0001g0208 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.136-4637C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477519 | |||||||
| chr19:18477572 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-4690G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477572 | |||||||
| chr19:18477941 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.136-5059C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477941 | |||||||
| chr19:18477990 | A | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.136-5108T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18477990 | |||||||
| chr19:18478191 | G | T | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.136-5309C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478191 | |||||||
| chr19:18478206 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.136-5324G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478206 | |||||||
| chr19:18478235 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-5353G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478235 | |||||||
| chr19:18478278 | T | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-5396A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478278 | |||||||
| chr19:18478280 | T | TA | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-5399dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478280 | |||||||
| chr19:18478551 | G | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-5669C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478551 | |||||||
| chr19:18478683 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.136-5801C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478683 | |||||||
| chr19:18478686 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136-5804G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478686 | |||||||
| chr19:18478722 | CCAGACCC others(10): Show |
C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-5857_136-5841d others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478722 | |||||||
| chr19:18478815 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-5933G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478815 | |||||||
| chr19:18478836 | A | T | 1 | a0001c0001t0002g0068 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136-5954T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478836 | |||||||
| chr19:18478847 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.136-5965C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478847 | |||||||
| chr19:18478976 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-6094C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18478976 | |||||||
| chr19:18479004 | C | T | 2 | a0001c0007t0009g0008 a0001c0007t0009g0009 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136-6122G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479004 | |||||||
| chr19:18479133 | C | T | 3 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0061 |
4 | HG01123.hp2 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-6251G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479133 | |||||||
| chr19:18479134 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-6252C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479134 | |||||||
| chr19:18479300 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-6418G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479300 | |||||||
| chr19:18479413 | C | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-6531G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479413 | |||||||
| chr19:18479441 | C | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.136-6559G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479441 | |||||||
| chr19:18479708 | C | CA | 33 | a0001c0001t0001g0144 a0001c0001t0002g0055 a0001c0001t0002g0086 others(30): Show |
33 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.136-6827dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | |||||||
| chr19:18479708 | C | CAAA | 7 | a0001c0001t0001g0147 a0001c0001t0001g0199 a0001c0001t0001g0212 others(4): Show |
7 | HG01167.hp2 HG02451.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.136-6829_136-6827d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | |||||||
| chr19:18479708 | C | CAAAA | 63 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(60): Show |
63 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-6830_136-6827d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | |||||||
| chr19:18479708 | C | CAAAAA | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(30): Show |
34 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.136-6831_136-6827d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18479708 | |||||||
| chr19:18480019 | T | C | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-7137A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480019 | |||||||
| chr19:18480059 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.136-7177A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480059 | |||||||
| chr19:18480159 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136-7277G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480159 | |||||||
| chr19:18480182 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-7300C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480182 | |||||||
| chr19:18480192 | C | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-7310G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480192 | |||||||
| chr19:18480911 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.136-8029C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480911 | |||||||
| chr19:18480923 | C | T | 7 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-8041G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480923 | |||||||
| chr19:18480928 | C | T | 5 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0230 others(2): Show |
5 | HG01109.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-8046G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480928 | |||||||
| chr19:18480935 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-8053C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18480935 | |||||||
| chr19:18481201 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-8319A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481201 | |||||||
| chr19:18481314 | G | A | 3 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 |
3 | HG00642.hp1 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.136-8432C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481314 | |||||||
| chr19:18481431 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-8549G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481431 | |||||||
| chr19:18481441 | C | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.136-8559G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481441 | |||||||
| chr19:18481457 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.136-8575C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481457 | |||||||
| chr19:18481514 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.136-8632C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481514 | |||||||
| chr19:18481743 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.136-8861C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481743 | |||||||
| chr19:18481971 | G | A | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9089C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18481971 | |||||||
| chr19:18482032 | T | C | 1 | a0002c0002t0001g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-9150A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482032 | |||||||
| chr19:18482240 | T | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0016 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136-9358A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482240 | |||||||
| chr19:18482307 | CCTTTTTT others(3): Show |
C | 4 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0142 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9435_136-9426d others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482307 | |||||||
| chr19:18482307 | CCTTTTTT others(4): Show |
C | 1 | a0002c0002t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136-9436_136-9426d others(13): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482307 | |||||||
| chr19:18482308 | C | CT | 15 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(12): Show |
15 | HG00738.hp1 HG01071.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.136-9427dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTT | 7 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0180 others(4): Show |
7 | HG01074.hp2 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-9428_136-9427d others(4): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTT | 45 | a0001c0001t0001g0003 a0001c0001t0001g0157 a0001c0001t0001g0168 others(42): Show |
46 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.136-9429_136-9427d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTTT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
25 | HG00280.hp2 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.136-9430_136-9427d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTTTT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0146 a0001c0001t0001g0155 others(11): Show |
14 | HG01109.hp1 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-9431_136-9427d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTTTTT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0194 a0001c0001t0001g0195 others(2): Show |
5 | HG02451.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9432_136-9427d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0225 a0001c0001t0002g0019 a0001c0001t0002g0029 others(5): Show |
8 | HG01361.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-9434_136-9427d others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-9439_136-9427d others(15): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | CTTTTTT | C | 33 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0017 others(30): Show |
33 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.136-9432_136-9427d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482308 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-9435_136-9427d others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482308 | |||||||
| chr19:18482322 | T | C | 1 | a0002c0002t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.136-9440A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482322 | |||||||
| chr19:18482343 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-9461C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482343 | |||||||
| chr19:18482349 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136-9467C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482349 | |||||||
| chr19:18482427 | C | CCTGCCT | 3 | a0001c0001t0004g0150 a0001c0007t0009g0008 a0002c0002t0019g0131 |
3 | HG01884.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.136-9551_136-9546d others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482427 | |||||||
| chr19:18482427 | C | CCTGCCTC others(5): Show |
4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-9557_136-9546d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482427 | |||||||
| chr19:18482526 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.136-9644G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482526 | |||||||
| chr19:18482537 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.136-9655G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482537 | |||||||
| chr19:18482598 | G | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-9716C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482598 | |||||||
| chr19:18482690 | T | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0237 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136-9808A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482690 | |||||||
| chr19:18482743 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.136-9861A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482743 | |||||||
| chr19:18482762 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-9880A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482762 | |||||||
| chr19:18482763 | T | G | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-9881A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | |||||||
| chr19:18482763 | T | TTTGTTGT others(2): Show |
16 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(13): Show |
16 | HG00323.hp2 HG01081.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.136-9890_136-9882d others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | |||||||
| chr19:18482763 | T | TTTGTTGT others(5): Show |
18 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0114 others(15): Show |
18 | HG00733.hp2 HG01258.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.136-9893_136-9882d others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | |||||||
| chr19:18482763 | T | TTTGTTGT others(8): Show |
9 | a0001c0001t0011g0115 a0002c0002t0001g0017 a0002c0002t0001g0126 others(6): Show |
9 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-9896_136-9882d others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482763 | |||||||
| chr19:18482794 | T | TTGCTGCT others(2): Show |
3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.136-9913_136-9912i others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482794 | T | TTGTTGCT others(2): Show |
6 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0155 others(3): Show |
6 | HG02055.hp2 HG02148.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482794 | T | TTGTTGCT others(5): Show |
1 | a0001c0001t0001g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136-9913_136-9912i others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482794 | T | TTGTTGTT others(5): Show |
85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(82): Show |
86 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482794 | T | TTGTTGTT others(8): Show |
9 | a0001c0001t0001g0005 a0001c0001t0001g0149 a0001c0001t0001g0168 others(6): Show |
9 | HG02886.hp1 HG03471.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-9913_136-9912i others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482794 | T | TTGTTGTT others(11): Show |
2 | a0001c0004t0006g0171 a0003c0006t0001g0211 |
2 | HG03041.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.136-9913_136-9912i others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482794 | |||||||
| chr19:18482797 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.136-9915G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482797 | |||||||
| chr19:18482914 | A | C | 1 | a0002c0002t0001g0240 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.136-10032T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482914 | |||||||
| chr19:18482916 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-10034G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18482916 | |||||||
| chr19:18483328 | A | G | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-10446T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483328 | |||||||
| chr19:18483438 | G | A | 1 | a0001c0004t0006g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.136-10556C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483438 | |||||||
| chr19:18483487 | C | T | 4 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-10605G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483487 | |||||||
| chr19:18483865 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136-10983C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483865 | |||||||
| chr19:18483904 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-11022G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18483904 | |||||||
| chr19:18484026 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-11144C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484026 | |||||||
| chr19:18484031 | C | T | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-11149G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484031 | |||||||
| chr19:18484172 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.136-11290C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484172 | |||||||
| chr19:18484229 | C | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-11347G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484229 | |||||||
| chr19:18484279 | C | T | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.136-11397G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484279 | |||||||
| chr19:18484339 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-11457G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484339 | |||||||
| chr19:18484354 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136-11472T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484354 | |||||||
| chr19:18484538 | G | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-11656C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484538 | |||||||
| chr19:18484568 | C | T | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-11686G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484568 | |||||||
| chr19:18484641 | A | G | 2 | a0002c0002t0005g0119 a0002c0002t0005g0120 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.136-11759T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484641 | |||||||
| chr19:18484710 | T | C | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.136-11828A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484710 | |||||||
| chr19:18484825 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
107 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.136-11943G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484825 | |||||||
| chr19:18484837 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.136-11955C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484837 | |||||||
| chr19:18484881 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-11999G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484881 | |||||||
| chr19:18484904 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-12022G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18484904 | |||||||
| chr19:18485012 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136-12130G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485012 | |||||||
| chr19:18485089 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-12207C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485089 | |||||||
| chr19:18485802 | C | G | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-12920G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485802 | |||||||
| chr19:18485818 | C | T | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-12936G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485818 | |||||||
| chr19:18485847 | G | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-12965C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485847 | |||||||
| chr19:18485847 | G | T | 1 | a0001c0001t0004g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.136-12965C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485847 | |||||||
| chr19:18485985 | CA | C | 6 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0076 others(3): Show |
6 | HG01099.hp1 HG01516.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-13104delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18485985 | |||||||
| chr19:18486001 | A | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0223 |
2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.136-13119T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486001 | |||||||
| chr19:18486174 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-13292C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486174 | |||||||
| chr19:18486203 | T | A | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.136-13321A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486203 | |||||||
| chr19:18486216 | T | C | 5 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-13334A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486216 | |||||||
| chr19:18486386 | G | A | 28 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0183 others(25): Show |
28 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-13504C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486386 | |||||||
| chr19:18486387 | G | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 |
3 | HG02132.hp1 NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.136-13505C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486387 | |||||||
| chr19:18486390 | G | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0042 |
2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.136-13508C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486390 | |||||||
| chr19:18486556 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136-13674C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486556 | |||||||
| chr19:18486608 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-13726C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486608 | |||||||
| chr19:18486649 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.136-13767C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486649 | |||||||
| chr19:18486651 | A | G | 1 | a0002c0002t0001g0017 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-13769T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486651 | |||||||
| chr19:18486763 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136-13881C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18486763 | |||||||
| chr19:18487021 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02055.hp2 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.136-14139G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487021 | |||||||
| chr19:18487164 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0091 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.136-14282C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487164 | |||||||
| chr19:18487363 | C | T | 5 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-14481G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487363 | |||||||
| chr19:18487403 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0011g0115 a0002c0002t0001g0014 others(42): Show |
45 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.136-14521A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18487403 | |||||||
| chr19:18488170 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-15288A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488170 | |||||||
| chr19:18488531 | C | T | 2 | a0002c0002t0005g0121 a0002c0002t0005g0127 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.136-15649G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488531 | |||||||
| chr19:18488557 | G | A | 2 | a0001c0001t0001g0206 a0001c0013t0001g0207 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.136-15675C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488557 | |||||||
| chr19:18488620 | C | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-15738G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488620 | |||||||
| chr19:18488647 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.136-15765A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488647 | |||||||
| chr19:18488759 | A | AG | 9 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-15878dupC | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488759 | |||||||
| chr19:18488929 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.136-16047G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488929 | |||||||
| chr19:18488947 | A | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-16065T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488947 | |||||||
| chr19:18488982 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.136-16100C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18488982 | |||||||
| chr19:18489006 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136-16124A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489006 | |||||||
| chr19:18489120 | G | A | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.136-16238C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489120 | |||||||
| chr19:18489148 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.136-16266A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489148 | |||||||
| chr19:18489151 | G | C | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.136-16269C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489151 | |||||||
| chr19:18489198 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.136-16316C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489198 | |||||||
| chr19:18489246 | G | A | 46 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(43): Show |
46 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.136-16364C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489246 | |||||||
| chr19:18489251 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136-16369G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489251 | |||||||
| chr19:18489260 | G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-16378C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489260 | |||||||
| chr19:18489372 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-16490C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489372 | |||||||
| chr19:18489461 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136-16579G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489461 | |||||||
| chr19:18489645 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-16763C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489645 | |||||||
| chr19:18489663 | C | T | 1 | a0001c0005t0007g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.136-16781G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18489663 | |||||||
| chr19:18490206 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-17324G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490206 | |||||||
| chr19:18490211 | C | G | 1 | a0001c0001t0003g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-17329G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490211 | |||||||
| chr19:18490310 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-17428G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490310 | |||||||
| chr19:18490360 | G | C | 1 | a0002c0002t0001g0015 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-17478C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490360 | |||||||
| chr19:18490361 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-17479C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490361 | |||||||
| chr19:18490449 | G | T | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-17567C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490449 | |||||||
| chr19:18490456 | C | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.136-17574G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490456 | |||||||
| chr19:18490722 | C | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-17840G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490722 | |||||||
| chr19:18490743 | G | C | 1 | a0001c0001t0002g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.136-17861C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18490743 | |||||||
| chr19:18491249 | ATT | A | 6 | a0001c0001t0002g0033 a0001c0001t0002g0056 a0001c0001t0002g0057 others(3): Show |
6 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-18369_136-1836 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTT | A | 7 | a0001c0001t0002g0001 a0001c0001t0002g0027 a0001c0001t0002g0030 others(4): Show |
8 | HG01975.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-18370_136-1836 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTT | A | 21 | a0001c0001t0002g0019 a0001c0001t0002g0029 a0001c0001t0002g0039 others(18): Show |
21 | HG00741.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.136-18371_136-1836 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTT | A | 17 | a0001c0001t0002g0031 a0001c0001t0002g0040 a0001c0001t0002g0041 others(14): Show |
17 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.136-18372_136-1836 others(9): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTT | A | 14 | a0001c0001t0002g0028 a0001c0001t0002g0046 a0001c0001t0002g0060 others(11): Show |
14 | HG00280.hp1 HG00642.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-18373_136-1836 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT | A | 13 | a0001c0001t0002g0026 a0001c0001t0002g0042 a0001c0001t0002g0047 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.136-18374_136-1836 others(11): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(6): Show |
A | 1 | a0002c0002t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136-18380_136-1836 others(17): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(7): Show |
A | 4 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0142 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-18381_136-1836 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(8): Show |
A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-18382_136-1836 others(19): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(10): Show |
A | 14 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0184 others(11): Show |
14 | HG01074.hp2 HG01099.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.136-18384_136-1836 others(21): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(12): Show |
A | 16 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0157 others(13): Show |
16 | HG01109.hp1 HG01167.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.136-18386_136-1836 others(23): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(13): Show |
A | 1 | a0002c0002t0001g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.136-18387_136-1836 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(14): Show |
A | 34 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(31): Show |
34 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.136-18388_136-1836 others(25): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(15): Show |
A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0061 others(3): Show |
7 | HG01123.hp2 HG02735.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-18389_136-1836 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(17): Show |
A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(19): Show |
22 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.136-18391_136-1836 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491249 | ATTTTTTT others(18): Show |
A | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136-18392_136-1836 others(29): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491249 | |||||||
| chr19:18491403 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.136-18521G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491403 | |||||||
| chr19:18491444 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-18562G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491444 | |||||||
| chr19:18491654 | C | T | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-18772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491654 | |||||||
| chr19:18491751 | C | CA | 5 | a0001c0001t0001g0205 a0001c0001t0001g0209 a0002c0002t0001g0137 others(2): Show |
5 | HG00735.hp2 HG01433.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-18870dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491751 | |||||||
| chr19:18491986 | T | G | 5 | a0001c0001t0002g0028 a0001c0001t0002g0083 a0001c0001t0002g0084 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-19104A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491986 | |||||||
| chr19:18491992 | G | C | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-19110C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18491992 | |||||||
| chr19:18492493 | A | C | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-19611T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492493 | |||||||
| chr19:18492494 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-19612G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492494 | |||||||
| chr19:18492651 | A | C | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-19769T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18492651 | |||||||
| chr19:18493131 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-20249G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493131 | |||||||
| chr19:18493211 | TGGGGCTG others(17): Show |
T | 1 | a0001c0001t0002g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136-20353_136-2033 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493211 | |||||||
| chr19:18493270 | C | T | 12 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(9): Show |
12 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.136-20388G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493270 | |||||||
| chr19:18493275 | C | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-20393G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493275 | |||||||
| chr19:18493344 | C | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.136-20462G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493344 | |||||||
| chr19:18493560 | C | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-20678G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493560 | |||||||
| chr19:18493635 | C | T | 2 | a0002c0002t0005g0119 a0002c0002t0005g0120 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.136-20753G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493635 | |||||||
| chr19:18493645 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0198 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.136-20763C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493645 | |||||||
| chr19:18493816 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136-20934G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493816 | |||||||
| chr19:18493895 | T | C | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-21013A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18493895 | |||||||
| chr19:18494068 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-21186T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494068 | |||||||
| chr19:18494132 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-21250A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494132 | |||||||
| chr19:18494175 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0198 a0001c0001t0014g0197 |
3 | HG01884.hp1 HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136-21293A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494175 | |||||||
| chr19:18494249 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.136-21367C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494249 | |||||||
| chr19:18494264 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-21382C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494264 | |||||||
| chr19:18494400 | G | GT | 5 | a0001c0001t0002g0105 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-21519dupA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494400 | |||||||
| chr19:18494643 | G | C | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-21761C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494643 | |||||||
| chr19:18494913 | T | C | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.136-22031A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18494913 | |||||||
| chr19:18495139 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.136-22257G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495139 | |||||||
| chr19:18495206 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.136-22324C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495206 | |||||||
| chr19:18495456 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
147 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.136-22574T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495456 | |||||||
| chr19:18495559 | G | T | 28 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(25): Show |
28 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.136-22677C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495559 | |||||||
| chr19:18495605 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-22723C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495605 | |||||||
| chr19:18495646 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.136-22764C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495646 | |||||||
| chr19:18495662 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.136-22780C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495662 | |||||||
| chr19:18495712 | C | A | 12 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(9): Show |
12 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-22830G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495712 | |||||||
| chr19:18495716 | T | G | 38 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(35): Show |
38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-22834A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495716 | |||||||
| chr19:18495784 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0220 |
3 | HG01891.hp1 HG02922.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.136-22902G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495784 | |||||||
| chr19:18495846 | G | A | 38 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(35): Show |
38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.136-22964C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18495846 | |||||||
| chr19:18496134 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.136-23252A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496134 | |||||||
| chr19:18496448 | T | TTCCTCTA others(1): Show |
3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.136-23574_136-2356 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496448 | |||||||
| chr19:18496527 | CT | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
148 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.136-23646delA | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496527 | |||||||
| chr19:18496583 | C | G | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-23701G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496583 | |||||||
| chr19:18496787 | A | G | 1 | a0002c0002t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.136-23905T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496787 | |||||||
| chr19:18496913 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(17): Show |
20 | HG01081.hp1 HG01891.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.136-24031C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496913 | |||||||
| chr19:18496970 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.136-24088G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496970 | |||||||
| chr19:18496985 | C | G | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-24103G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18496985 | |||||||
| chr19:18497337 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.136-24455T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497337 | |||||||
| chr19:18497353 | G | A | 1 | a0005c0011t0001g0159 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136-24471C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497353 | |||||||
| chr19:18497384 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0229 |
2 | HG01255.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.136-24502A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497384 | |||||||
| chr19:18497409 | G | A | 4 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+24512C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497409 | |||||||
| chr19:18497473 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.135+24448G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497473 | |||||||
| chr19:18497557 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+24364G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497557 | |||||||
| chr19:18497708 | C | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+24213G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497708 | |||||||
| chr19:18497769 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+24152C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497769 | |||||||
| chr19:18497815 | C | CA | 44 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0147 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+24105dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | |||||||
| chr19:18497815 | CA | C | 16 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0155 others(13): Show |
16 | HG00738.hp1 HG01167.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+24105delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | |||||||
| chr19:18497815 | CAA | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
76 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.135+24104_135+2410 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | |||||||
| chr19:18497815 | CAAA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0182 a0001c0001t0001g0191 others(2): Show |
5 | HG01109.hp1 HG02293.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+24103_135+2410 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18497815 | |||||||
| chr19:18498280 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+23641A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498280 | |||||||
| chr19:18498552 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.135+23369T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498552 | |||||||
| chr19:18498563 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+23358C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498563 | |||||||
| chr19:18498651 | A | G | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+23270T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498651 | |||||||
| chr19:18498954 | AAAC | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+22964_135+2296 others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18498954 | |||||||
| chr19:18499706 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.135+22215T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18499706 | |||||||
| chr19:18499721 | C | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0037 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.135+22200G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18499721 | |||||||
| chr19:18500006 | A | T | 10 | a0001c0001t0002g0033 a0001c0001t0002g0051 a0001c0001t0002g0052 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+21915T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500006 | |||||||
| chr19:18500210 | T | C | 2 | a0002c0002t0001g0240 a0002c0002t0001g0241 |
2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.135+21711A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500210 | |||||||
| chr19:18500234 | C | G | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+21687G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500234 | |||||||
| chr19:18500261 | C | CA | 14 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0233 others(11): Show |
14 | HG01109.hp1 HG01175.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.135+21659dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500261 | |||||||
| chr19:18500310 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+21611C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500310 | |||||||
| chr19:18500321 | T | C | 1 | a0001c0001t0002g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.135+21600A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500321 | |||||||
| chr19:18500337 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+21584T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500337 | |||||||
| chr19:18500372 | A | C | 1 | a0001c0001t0002g0050 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.135+21549T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500372 | |||||||
| chr19:18500446 | C | T | 1 | a0001c0003t0001g0161 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.135+21475G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500446 | |||||||
| chr19:18500556 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+21365C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500556 | |||||||
| chr19:18500689 | G | A | 1 | a0001c0010t0002g0032 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.135+21232C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500689 | |||||||
| chr19:18500735 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+21186G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500735 | |||||||
| chr19:18500740 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+21181A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500740 | |||||||
| chr19:18500816 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0198 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.135+21105G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18500816 | |||||||
| chr19:18501011 | C | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+20910G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501011 | |||||||
| chr19:18501085 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+20836G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501085 | |||||||
| chr19:18501382 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+20539G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501382 | |||||||
| chr19:18501387 | G | A | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+20534C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501387 | |||||||
| chr19:18501447 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.135+20474C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501447 | |||||||
| chr19:18501541 | G | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+20380C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501541 | |||||||
| chr19:18501542 | G | A | 1 | a0002c0002t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+20379C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501542 | |||||||
| chr19:18501819 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+20102G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501819 | |||||||
| chr19:18501827 | G | A | 6 | a0001c0001t0011g0115 a0002c0002t0005g0119 a0002c0002t0005g0120 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+20094C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501827 | |||||||
| chr19:18501938 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+19983C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501938 | |||||||
| chr19:18501948 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(145): Show |
149 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.135+19973C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18501948 | |||||||
| chr19:18502042 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.135+19879G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502042 | |||||||
| chr19:18502112 | T | C | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+19809A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502112 | |||||||
| chr19:18502180 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.135+19741C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502180 | |||||||
| chr19:18502222 | C | G | 2 | a0001c0007t0009g0008 a0001c0007t0009g0009 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+19699G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502222 | |||||||
| chr19:18502673 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.135+19248G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502673 | |||||||
| chr19:18502833 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.135+19088G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502833 | |||||||
| chr19:18502842 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+19079G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18502842 | |||||||
| chr19:18503079 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.135+18842G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503079 | |||||||
| chr19:18503107 | C | T | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0099 |
3 | HG00735.hp1 HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.135+18814G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503107 | |||||||
| chr19:18503125 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18796C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503125 | |||||||
| chr19:18503383 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18538G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503383 | |||||||
| chr19:18503613 | A | G | 46 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0011g0115 others(43): Show |
46 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.135+18308T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503613 | |||||||
| chr19:18503620 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.135+18301G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503620 | |||||||
| chr19:18503751 | C | G | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+18170G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503751 | |||||||
| chr19:18503780 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.135+18141G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18503780 | |||||||
| chr19:18504045 | G | A | 3 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0099 |
3 | HG00735.hp1 HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.135+17876C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504045 | |||||||
| chr19:18504125 | T | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
101 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.135+17796A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504125 | |||||||
| chr19:18504187 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.135+17734G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504187 | |||||||
| chr19:18504460 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+17461G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504460 | |||||||
| chr19:18504552 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.135+17369A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504552 | |||||||
| chr19:18504615 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(1): Show |
4 | HG02559.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+17306G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504615 | |||||||
| chr19:18504634 | C | T | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+17287G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504634 | |||||||
| chr19:18504660 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+17261G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504660 | |||||||
| chr19:18504690 | T | A | 1 | a0001c0001t0003g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+17231A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504690 | |||||||
| chr19:18504852 | G | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+17069C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18504852 | |||||||
| chr19:18505091 | G | A | 2 | a0002c0002t0001g0111 a0002c0002t0001g0134 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.135+16830C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505091 | |||||||
| chr19:18505097 | G | A | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+16824C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505097 | |||||||
| chr19:18505202 | C | G | 2 | a0002c0002t0001g0111 a0002c0002t0001g0134 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.135+16719G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505202 | |||||||
| chr19:18505589 | T | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+16332A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505589 | |||||||
| chr19:18505714 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+16207C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18505714 | |||||||
| chr19:18506163 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0018g0196 a0001c0013t0001g0207 |
3 | HG01516.hp1 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.135+15758G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506163 | |||||||
| chr19:18506339 | C | T | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.135+15582G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506339 | |||||||
| chr19:18506341 | G | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+15580C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506341 | |||||||
| chr19:18506544 | C | T | 1 | a0001c0001t0002g0039 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135+15377G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506544 | |||||||
| chr19:18506575 | A | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(1): Show |
4 | HG00738.hp2 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+15346T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506575 | |||||||
| chr19:18506983 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.135+14938C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18506983 | |||||||
| chr19:18507007 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.135+14914T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507007 | |||||||
| chr19:18507026 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.135+14895G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507026 | |||||||
| chr19:18507302 | T | C | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+14619A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507302 | |||||||
| chr19:18507415 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+14506G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507415 | |||||||
| chr19:18507507 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.135+14414G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507507 | |||||||
| chr19:18507634 | G | A | 1 | a0002c0002t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.135+14287C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507634 | |||||||
| chr19:18507638 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+14283T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507638 | |||||||
| chr19:18507755 | T | C | 9 | a0001c0001t0002g0035 a0001c0001t0002g0088 a0001c0001t0002g0089 others(6): Show |
9 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+14166A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507755 | |||||||
| chr19:18507759 | T | C | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+14162A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507759 | |||||||
| chr19:18507770 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+14151G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18507770 | |||||||
| chr19:18508057 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+13864C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508057 | |||||||
| chr19:18508213 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+13708G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508213 | |||||||
| chr19:18508246 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0042 |
2 | HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.135+13675G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508246 | |||||||
| chr19:18508247 | T | C | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+13674A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508247 | |||||||
| chr19:18508354 | A | G | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(1): Show |
4 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+13567T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508354 | |||||||
| chr19:18508391 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+13530A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508391 | |||||||
| chr19:18508524 | G | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 |
3 | HG02132.hp1 NA18951.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.135+13397C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508524 | |||||||
| chr19:18508587 | G | A | 1 | a0001c0001t0011g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+13334C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508587 | |||||||
| chr19:18508841 | C | T | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+13080G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508841 | |||||||
| chr19:18508927 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+12994G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18508927 | |||||||
| chr19:18509058 | C | T | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+12863G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509058 | |||||||
| chr19:18509120 | T | A | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+12801A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509120 | |||||||
| chr19:18509373 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.135+12548A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509373 | |||||||
| chr19:18509440 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.135+12481C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509440 | |||||||
| chr19:18509575 | ATGCACG | A | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+12340_135+1234 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509575 | |||||||
| chr19:18509582 | T | TGC | 3 | a0002c0002t0001g0112 a0002c0002t0001g0114 a0002c0002t0013g0113 |
3 | HG01081.hp2 HG01496.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.135+12337_135+1233 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | |||||||
| chr19:18509582 | T | TGCGCGCG others(3): Show |
1 | a0002c0002t0001g0129 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135+12329_135+1233 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | |||||||
| chr19:18509582 | T | TGCGCGCG others(5): Show |
2 | a0002c0002t0001g0111 a0002c0002t0001g0130 |
2 | HG02559.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.135+12327_135+1233 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | |||||||
| chr19:18509582 | T | TGCGCGCG others(9): Show |
1 | a0002c0002t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.135+12338_135+1233 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | |||||||
| chr19:18509582 | T | TGTGCGCA others(11): Show |
1 | a0001c0001t0001g0157 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+12338_135+1233 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509582 | |||||||
| chr19:18509584 | C | T | 1 | a0002c0002t0005g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135+12337G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509584 | |||||||
| chr19:18509585 | G | A | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12336C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509585 | |||||||
| chr19:18509590 | C | T | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+12331G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509590 | |||||||
| chr19:18509591 | GCGCACAT others(7): Show |
G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0210 a0003c0006t0001g0211 |
3 | HG01167.hp1 HG01928.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.135+12316_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(9): Show |
G | 6 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0232 others(3): Show |
6 | HG01099.hp2 HG01433.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+12314_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(11): Show |
G | 8 | a0001c0001t0001g0183 a0001c0001t0001g0200 a0001c0001t0001g0201 others(5): Show |
8 | HG00280.hp2 HG00408.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12312_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(13): Show |
G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01884.hp1 NA18951.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12310_135+1232 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(15): Show |
G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0179 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+12308_135+1232 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(17): Show |
G | 8 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
8 | HG01109.hp1 HG01952.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12306_135+1232 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(19): Show |
G | 2 | a0001c0001t0011g0115 a0001c0001t0017g0189 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.135+12304_135+1232 others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509591 | GCGCACAT others(21): Show |
G | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+12302_135+1232 others(32): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509591 | |||||||
| chr19:18509592 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+12329G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509592 | |||||||
| chr19:18509593 | GCACATAC others(1): Show |
G | 8 | a0001c0001t0001g0156 a0001c0001t0004g0152 a0002c0002t0001g0015 others(5): Show |
8 | HG01167.hp2 HG01258.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12320_135+1232 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(3): Show |
G | 3 | a0002c0002t0001g0117 a0002c0002t0001g0134 a0002c0002t0008g0118 |
3 | HG01346.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.135+12318_135+1232 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(5): Show |
G | 7 | a0001c0001t0016g0173 a0001c0004t0006g0170 a0001c0004t0006g0172 others(4): Show |
7 | HG02004.hp1 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+12316_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(7): Show |
G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0219 a0001c0004t0006g0171 others(1): Show |
4 | HG02970.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12314_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(9): Show |
G | 4 | a0001c0001t0001g0178 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG02300.hp2 HG02572.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12312_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(11): Show |
G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(9): Show |
12 | HG00733.hp2 HG01891.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+12310_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(13): Show |
G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0225 others(4): Show |
7 | HG00642.hp2 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+12308_135+1232 others(24): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(15): Show |
G | 17 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0166 others(14): Show |
17 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.135+12306_135+1232 others(26): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(17): Show |
G | 5 | a0001c0001t0001g0147 a0001c0001t0001g0213 a0001c0001t0004g0151 others(2): Show |
5 | HG01123.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12304_135+1232 others(28): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(19): Show |
G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0155 others(3): Show |
6 | HG01081.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+12302_135+1232 others(30): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(21): Show |
G | 2 | a0001c0005t0007g0176 a0002c0002t0001g0143 |
2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.135+12300_135+1232 others(32): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(23): Show |
G | 2 | a0001c0005t0007g0174 a0001c0005t0007g0175 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.135+12298_135+1232 others(34): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509593 | GCACATAC others(25): Show |
G | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+12296_135+1232 others(36): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509593 | |||||||
| chr19:18509594 | CACAT | C | 4 | a0002c0002t0001g0016 a0002c0002t0001g0110 a0002c0002t0001g0125 others(1): Show |
4 | HG02896.hp2 HG03471.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12323_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509594 | |||||||
| chr19:18509595 | A | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12326T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509595 | |||||||
| chr19:18509595 | A | G | 11 | a0001c0001t0004g0154 a0002c0002t0001g0109 a0002c0002t0001g0112 others(8): Show |
11 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+12326T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509595 | |||||||
| chr19:18509596 | C | G | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12325G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509596 | |||||||
| chr19:18509597 | A | C | 1 | a0002c0002t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.135+12324T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509597 | |||||||
| chr19:18509597 | A | G | 12 | a0001c0001t0004g0154 a0002c0002t0001g0109 a0002c0002t0001g0112 others(9): Show |
12 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.135+12324T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509597 | |||||||
| chr19:18509598 | T | C | 15 | a0001c0001t0001g0157 a0001c0001t0004g0154 a0002c0002t0001g0017 others(12): Show |
15 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+12323A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | T | TAC | 10 | a0001c0001t0002g0033 a0001c0001t0002g0053 a0001c0001t0002g0068 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+12321_135+1232 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | T | TACAC | 8 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0055 others(5): Show |
8 | HG01069.hp2 HG01074.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+12319_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | T | TACACAC | 3 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0002g0094 |
3 | HG01257.hp1 HG02148.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.135+12317_135+1232 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | T | TACACACA others(5): Show |
2 | a0001c0001t0002g0074 a0001c0001t0002g0095 |
2 | HG01175.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.135+12311_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | T | TACACACA others(9): Show |
1 | a0001c0001t0002g0051 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.135+12307_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TAC | T | 10 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0042 others(7): Show |
10 | HG00639.hp2 HG01515.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+12321_135+1232 others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACAC | T | 7 | a0001c0001t0002g0028 a0001c0001t0002g0035 a0001c0001t0002g0076 others(4): Show |
7 | HG00639.hp1 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+12319_135+1232 others(8): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACAC | T | 9 | a0001c0001t0002g0034 a0001c0001t0002g0041 a0001c0001t0002g0061 others(6): Show |
9 | HG00280.hp1 HG00738.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+12317_135+1232 others(10): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(1): Show |
T | 9 | a0001c0001t0002g0040 a0001c0001t0002g0047 a0001c0001t0002g0048 others(6): Show |
9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+12315_135+1232 others(12): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(3): Show |
T | 11 | a0001c0001t0002g0019 a0001c0001t0002g0027 a0001c0001t0002g0029 others(8): Show |
11 | HG02300.hp1 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+12313_135+1232 others(14): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(5): Show |
T | 2 | a0001c0001t0003g0025 a0001c0001t0015g0065 |
2 | HG01975.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.135+12311_135+1232 others(16): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(7): Show |
T | 3 | a0001c0001t0002g0002 a0001c0001t0003g0023 a0001c0001t0003g0024 |
3 | HG02818.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.135+12309_135+1232 others(18): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(9): Show |
T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(1): Show |
4 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+12307_135+1232 others(20): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(11): Show |
T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0093 |
2 | HG00733.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.135+12305_135+1232 others(22): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509598 | TACACACA others(33): Show |
T | 4 | a0001c0001t0002g0001 a0001c0001t0002g0050 a0001c0001t0002g0108 others(1): Show |
5 | NA18975.hp1 NA19060.hp2 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12283_135+1232 others(44): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509598 | |||||||
| chr19:18509599 | A | G | 13 | a0001c0001t0004g0154 a0002c0002t0001g0110 a0002c0002t0001g0112 others(10): Show |
13 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.135+12322T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509599 | |||||||
| chr19:18509601 | A | G | 15 | a0001c0001t0004g0153 a0001c0001t0004g0154 a0002c0002t0001g0110 others(12): Show |
15 | HG01081.hp2 HG01169.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+12320T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509601 | |||||||
| chr19:18509603 | A | G | 16 | a0001c0001t0001g0156 a0001c0001t0004g0152 a0001c0001t0004g0153 others(13): Show |
16 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+12318T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509603 | |||||||
| chr19:18509605 | A | G | 16 | a0001c0001t0001g0156 a0001c0001t0004g0152 a0001c0001t0004g0153 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+12316T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509605 | |||||||
| chr19:18509607 | A | G | 21 | a0001c0001t0004g0152 a0001c0001t0004g0153 a0001c0001t0004g0154 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+12314T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509607 | |||||||
| chr19:18509609 | A | G | 21 | a0001c0001t0004g0152 a0001c0001t0004g0153 a0001c0001t0004g0154 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+12312T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509609 | |||||||
| chr19:18509611 | A | G | 20 | a0001c0001t0004g0152 a0001c0001t0004g0153 a0001c0001t0004g0154 others(17): Show |
20 | HG01167.hp2 HG01169.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+12310T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509611 | |||||||
| chr19:18509613 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
23 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+12308T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509613 | |||||||
| chr19:18509615 | A | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0149 others(14): Show |
17 | HG01346.hp2 HG02004.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.135+12306T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509615 | |||||||
| chr19:18509617 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0002g0007 others(8): Show |
11 | HG02004.hp1 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+12304T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509617 | |||||||
| chr19:18509619 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0149 a0001c0001t0001g0185 others(16): Show |
20 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+12302T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509619 | |||||||
| chr19:18509621 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0155 others(5): Show |
8 | HG02717.hp2 HG02738.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+12300T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509621 | |||||||
| chr19:18509623 | A | G | 5 | a0001c0001t0001g0144 a0001c0001t0001g0155 a0001c0001t0001g0168 others(2): Show |
5 | HG02738.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+12298T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509623 | |||||||
| chr19:18509625 | A | G | 4 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+12296T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509625 | |||||||
| chr19:18509627 | A | G | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0002c0002t0001g0137 |
3 | HG02622.hp1 HG02647.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.135+12294T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509627 | |||||||
| chr19:18509629 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+12292T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509629 | |||||||
| chr19:18509631 | A | G | 1 | a0002c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+12290T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509631 | |||||||
| chr19:18509916 | A | T | 1 | a0002c0002t0001g0114 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.135+12005T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509916 | |||||||
| chr19:18509975 | G | T | 4 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(1): Show |
4 | HG02809.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+11946C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18509975 | |||||||
| chr19:18510057 | C | A | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+11864G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510057 | |||||||
| chr19:18510239 | G | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+11682C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510239 | |||||||
| chr19:18510536 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+11385A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510536 | |||||||
| chr19:18510612 | G | A | 4 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG00733.hp1 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+11309C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510612 | |||||||
| chr19:18510732 | C | T | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+11189G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510732 | |||||||
| chr19:18510769 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.135+11152T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510769 | |||||||
| chr19:18510809 | T | C | 11 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0164 others(8): Show |
11 | HG01081.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.135+11112A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510809 | |||||||
| chr19:18510860 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+11061T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510860 | |||||||
| chr19:18510869 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+11052G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18510869 | |||||||
| chr19:18511184 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+10737T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511184 | |||||||
| chr19:18511193 | G | C | 3 | a0002c0002t0001g0111 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | HG02559.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135+10728C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511193 | |||||||
| chr19:18511303 | G | A | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+10618C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511303 | |||||||
| chr19:18511383 | T | C | 44 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+10538A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511383 | |||||||
| chr19:18511405 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10516G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511405 | |||||||
| chr19:18511541 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.135+10380C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511541 | |||||||
| chr19:18511614 | C | T | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+10307G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511614 | |||||||
| chr19:18511633 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10288G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511633 | |||||||
| chr19:18511873 | A | AT | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+10047_135+1004 others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511873 | |||||||
| chr19:18511873 | A | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
146 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.135+10048T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511873 | |||||||
| chr19:18511889 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+10032T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511889 | |||||||
| chr19:18511996 | A | G | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+9925T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18511996 | |||||||
| chr19:18512029 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+9892G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512029 | |||||||
| chr19:18512149 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+9772G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512149 | |||||||
| chr19:18512154 | C | CA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+9766dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512154 | |||||||
| chr19:18512322 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+9599C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512322 | |||||||
| chr19:18512388 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+9533C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512388 | |||||||
| chr19:18512635 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.135+9286G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512635 | |||||||
| chr19:18512647 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.135+9274G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512647 | |||||||
| chr19:18512951 | G | A | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8970C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18512951 | |||||||
| chr19:18513041 | G | A | 1 | a0002c0002t0001g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135+8880C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513041 | |||||||
| chr19:18513108 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.135+8813A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513108 | |||||||
| chr19:18513271 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.135+8650C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513271 | |||||||
| chr19:18513279 | G | A | 1 | a0001c0001t0012g0228 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.135+8642C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513279 | |||||||
| chr19:18513361 | G | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+8560C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513361 | |||||||
| chr19:18513479 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG01891.hp1 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.135+8442T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513479 | |||||||
| chr19:18513523 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
152 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.135+8398T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513523 | |||||||
| chr19:18513580 | T | G | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8341A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513580 | |||||||
| chr19:18513590 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.135+8331A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513590 | |||||||
| chr19:18513669 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+8252G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513669 | |||||||
| chr19:18513796 | T | C | 7 | a0001c0001t0001g0144 a0001c0004t0006g0170 a0001c0004t0006g0171 others(4): Show |
7 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+8125A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18513796 | |||||||
| chr19:18514154 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+7767C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514154 | |||||||
| chr19:18514341 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+7580T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514341 | |||||||
| chr19:18514370 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.135+7551G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514370 | |||||||
| chr19:18514383 | G | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0100 a0001c0001t0002g0101 |
3 | HG01243.hp1 HG01496.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.135+7538C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514383 | |||||||
| chr19:18514500 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+7421A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514500 | |||||||
| chr19:18514513 | C | CA | 16 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(13): Show |
16 | HG01261.hp1 HG01261.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.135+7407dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514513 | |||||||
| chr19:18514513 | CA | C | 15 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(12): Show |
15 | HG01099.hp1 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+7407delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18514513 | |||||||
| chr19:18515128 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+6793G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515128 | |||||||
| chr19:18515146 | C | T | 2 | a0001c0007t0009g0008 a0001c0007t0009g0009 |
2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.135+6775G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515146 | |||||||
| chr19:18515566 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+6355C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515566 | |||||||
| chr19:18515713 | T | C | 1 | a0001c0001t0016g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135+6208A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515713 | |||||||
| chr19:18515922 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5999G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18515922 | |||||||
| chr19:18516109 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0002g0007 |
2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.135+5812G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516109 | |||||||
| chr19:18516257 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+5664A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516257 | |||||||
| chr19:18516310 | A | T | 1 | a0001c0001t0002g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.135+5611T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516310 | |||||||
| chr19:18516323 | C | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5598G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516323 | |||||||
| chr19:18516331 | C | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+5590G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516331 | |||||||
| chr19:18516424 | C | G | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+5497G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516424 | |||||||
| chr19:18516561 | G | GC | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+5359dupG | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516561 | |||||||
| chr19:18516667 | C | G | 2 | a0002c0002t0001g0112 a0002c0002t0013g0113 |
2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.135+5254G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516667 | |||||||
| chr19:18516859 | G | A | 1 | a0001c0005t0007g0176 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.135+5062C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516859 | |||||||
| chr19:18516910 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.135+5011G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516910 | |||||||
| chr19:18516989 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+4932C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18516989 | |||||||
| chr19:18517143 | A | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.135+4778T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517143 | |||||||
| chr19:18517165 | G | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(17): Show |
20 | HG01081.hp1 HG01891.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+4756C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517165 | |||||||
| chr19:18517263 | C | T | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4658G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517263 | |||||||
| chr19:18517267 | T | C | 1 | a0007c0014t0001g0013 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.135+4654A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517267 | |||||||
| chr19:18517334 | T | C | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+4587A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517334 | |||||||
| chr19:18517395 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+4526A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517395 | |||||||
| chr19:18517433 | T | C | 3 | a0001c0004t0006g0170 a0001c0004t0006g0171 a0001c0004t0006g0172 |
3 | HG02886.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.135+4488A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517433 | |||||||
| chr19:18517445 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.135+4476A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517445 | |||||||
| chr19:18517465 | G | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+4456C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517465 | |||||||
| chr19:18517544 | C | T | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+4377G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517544 | |||||||
| chr19:18517636 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.135+4285C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517636 | |||||||
| chr19:18517706 | A | T | 41 | a0001c0001t0011g0115 a0002c0002t0001g0014 a0002c0002t0001g0015 others(38): Show |
41 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.135+4215T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517706 | |||||||
| chr19:18517707 | T | A | 2 | a0001c0001t0001g0232 a0001c0001t0002g0103 |
2 | HG01099.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.135+4214A>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517707 | |||||||
| chr19:18517808 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+4113C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517808 | |||||||
| chr19:18517886 | C | CA | 44 | a0001c0001t0011g0115 a0001c0005t0007g0174 a0001c0005t0007g0175 others(41): Show |
44 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.135+4034dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517886 | |||||||
| chr19:18517886 | CA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0177 a0001c0001t0002g0026 others(2): Show |
5 | HG01169.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+4034delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18517886 | |||||||
| chr19:18518019 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+3902C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518019 | |||||||
| chr19:18518079 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+3842C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518079 | |||||||
| chr19:18518110 | T | C | 3 | a0001c0005t0007g0174 a0001c0005t0007g0175 a0001c0005t0007g0176 |
3 | HG02622.hp1 HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.135+3811A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518110 | |||||||
| chr19:18518137 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+3784T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518137 | |||||||
| chr19:18518302 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+3619A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518302 | |||||||
| chr19:18518323 | G | A | 5 | a0002c0002t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+3598C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518323 | |||||||
| chr19:18518425 | G | A | 1 | a0001c0001t0002g0104 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.135+3496C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518425 | |||||||
| chr19:18518465 | G | A | 3 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 |
3 | HG02735.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.135+3456C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518465 | |||||||
| chr19:18518467 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+3454T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518467 | |||||||
| chr19:18518483 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+3438G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518483 | |||||||
| chr19:18518489 | C | CA | 50 | a0001c0001t0001g0144 a0001c0001t0001g0234 a0001c0001t0002g0105 others(47): Show |
50 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.135+3431dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518489 | |||||||
| chr19:18518489 | CA | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0155 a0001c0001t0001g0156 others(4): Show |
7 | HG01169.hp2 HG02055.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+3431delT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518489 | |||||||
| chr19:18518603 | C | T | 7 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
7 | HG01361.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3318G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518603 | |||||||
| chr19:18518716 | G | A | 1 | a0001c0004t0006g0172 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.135+3205C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518716 | |||||||
| chr19:18518787 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.135+3134A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18518787 | |||||||
| chr19:18519020 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+2901A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519020 | |||||||
| chr19:18519093 | T | G | 5 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2828A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519093 | |||||||
| chr19:18519100 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
29 | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.135+2821G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519100 | |||||||
| chr19:18519197 | A | C | 1 | a0001c0001t0002g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.135+2724T>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519197 | |||||||
| chr19:18519229 | C | A | 1 | a0001c0001t0002g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.135+2692G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519229 | |||||||
| chr19:18519449 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+2472C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519449 | |||||||
| chr19:18519457 | C | T | 2 | a0002c0002t0001g0238 a0002c0002t0001g0239 |
2 | HG00323.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.135+2464G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519457 | |||||||
| chr19:18519664 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.135+2257C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519664 | |||||||
| chr19:18519755 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG01891.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.135+2166G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519755 | |||||||
| chr19:18519770 | T | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+2151A>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519770 | |||||||
| chr19:18519806 | C | CA | 5 | a0001c0001t0002g0108 a0002c0002t0001g0140 a0002c0002t0001g0141 others(2): Show |
5 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2114dupT | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519806 | |||||||
| chr19:18519820 | AAAAAG | A | 8 | a0001c0001t0001g0169 a0001c0001t0001g0235 a0001c0001t0001g0236 others(5): Show |
8 | HG01975.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+2096_135+2100d others(7): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519820 | |||||||
| chr19:18519821 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.135+2100T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519821 | |||||||
| chr19:18519821 | AAAAG | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
89 | HG00280.hp2 HG00642.hp2 HG01069.hp1 others(86): Show |
intron_variant | MODIFIER | c.135+2096_135+2099d others(6): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519821 | |||||||
| chr19:18519822 | AAAG | A | 5 | a0001c0001t0001g0177 a0001c0001t0001g0202 a0001c0001t0001g0204 others(2): Show |
5 | HG00408.hp2 HG00735.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+2096_135+2098d others(5): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519822 | |||||||
| chr19:18519892 | A | T | 5 | a0001c0001t0004g0150 a0001c0001t0004g0151 a0001c0001t0004g0152 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+2029T>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18519892 | |||||||
| chr19:18520446 | G | C | 4 | a0001c0001t0001g0144 a0001c0005t0007g0174 a0001c0005t0007g0175 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+1475C>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520446 | |||||||
| chr19:18520522 | C | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.135+1399G>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520522 | |||||||
| chr19:18520663 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.135+1258C>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520663 | |||||||
| chr19:18520821 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0001t0001g0178 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.135+1100C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520821 | |||||||
| chr19:18520910 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0005 |
2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.135+1011G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520910 | |||||||
| chr19:18520984 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+937G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18520984 | |||||||
| chr19:18521007 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.135+914T>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521007 | |||||||
| chr19:18521035 | C | G | 4 | a0002c0002t0001g0238 a0002c0002t0001g0239 a0002c0002t0001g0240 others(1): Show |
4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+886G>C | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521035 | |||||||
| chr19:18521414 | C | T | 5 | a0002c0002t0001g0014 a0002c0002t0001g0015 a0002c0002t0001g0016 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+507G>A | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521414 | |||||||
| chr19:18521415 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
106 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.135+506A>G | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521415 | |||||||
| chr19:18521650 | G | A | 4 | a0002c0002t0001g0238 a0002c0002t0001g0239 a0002c0002t0001g0240 others(1): Show |
4 | HG00323.hp2 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+271C>T | ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521650 | |||||||
| chr19:18521678 | CGA | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(7): Show |
10 | HG01891.hp1 HG02280.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.135+241_135+242del others(2): Show |
ELL | ENSG00000105656.13 | transcript | ENST00000262809.9 | protein_coding | 1/11 | chr19 | 18521678 |