Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4861 |
| ensemblid | ENSG00000130751.10 |
| hgncid | 7894 |
| symbol | NPAS1 |
| name | neuronal PAS domain protein 1 |
| refseq_nuc | NM_002517.4 |
| refseq_prot | NP_002508.2 |
| ensembl_nuc | ENST00000602212.6 |
| ensembl_prot | ENSP00000469142.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 47019837 |
| end | 47045775 |
| strand | + |
| ver | v1.2 |
| region | chr19:47019837-47045775 |
| region5000 | chr19:47014837-47050775 |
| regionname0 | NPAS1_chr19_47019837_47045775 |
| regionname5000 | NPAS1_chr19_47014837_47050775 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 590 | 411 | 97 | 75 | 173 | 18 | 46 | 125 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0002 | 0/0 | 590 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0003 | 0/0 | 590 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0004 | 0/0 | 590 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0005 | 0/0 | 590 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0006 | 0/0 | 590 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| a0007 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | MAAPY others(585): Show |
chr19 | 47014837 | 47050775 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1770 | 204 | 16 | 35 | 126 | 10 | 17 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0002 | 1/0 | 1770 | 136 | 47 | 22 | 40 | 7 | 19 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0003 | 0/1 | 1770 | 45 | 15 | 15 | 3 | 1 | 10 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0004 | 0/0 | 1770 | 13 | 13 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0005 | 0/0 | 1770 | 4 | 2 | 2 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0007 | 0/0 | 1770 | 2 | 1 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0008 | 0/0 | 1770 | 2 | 1 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0013 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0014 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0016 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0017 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0001c0018 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0002c0006 | 0/0 | 1770 | 2 | 0 | 0 | 0 | 0 | 2 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0003c0009 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0004c0015 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0005c0010 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0006c0011 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 | ||
| a0007c0012 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | ATGGC others(1765): Show |
chr19 | 47014837 | 47050775 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2100 | 197 | 16 | 31 | 123 | 10 | 17 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0001t0002 | 0/0 | 2100 | 4 | 0 | 4 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0001t0003 | 0/0 | 2100 | 3 | 0 | 0 | 3 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0002t0001 | 1/0 | 2100 | 134 | 45 | 22 | 40 | 7 | 19 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0002t0004 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0003t0001 | 0/1 | 2100 | 45 | 15 | 15 | 3 | 1 | 10 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0004t0001 | 0/0 | 2100 | 13 | 13 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0005t0001 | 0/0 | 2100 | 4 | 2 | 2 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0007t0001 | 0/0 | 2100 | 2 | 1 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0008t0001 | 0/0 | 2100 | 2 | 1 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0013t0001 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0014t0001 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0016t0001 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0017t0001 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0001c0018t0001 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0002c0006t0001 | 0/0 | 2100 | 2 | 0 | 0 | 0 | 0 | 2 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0003c0009t0001 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0004c0015t0001 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0005c0010t0001 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0006c0011t0001 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| a0007c0012t0001 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | GCCGA others(2095): Show |
chr19 | 47014837 | 47050775 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0403 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0001g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0404 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0002t0004g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0385 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0003t0001g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0004t0001g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0005t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0005t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0007t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0008t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0008t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0013t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0014t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0016t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0017t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0001c0018t0001g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0002c0006t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0003c0009t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0004c0015t0001g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0005c0010t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0006c0011t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| a0007c0012t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0205 | EUR | GBR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0017 | EUR | GBR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0314 | EUR | FIN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0168 | EUR | FIN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0368 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00621 | hp2 | a0001 | c0014 | t0001 | g0362 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00642 | hp2 | a0001 | c0005 | t0001 | g0327 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0224 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0402 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00741 | hp1 | a0003 | c0009 | t0001 | g0255 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01070 | hp1 | a0001 | c0005 | t0001 | g0301 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0296 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01243 | hp2 | a0001 | c0008 | t0001 | g0324 | AMR | PUR | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0136 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0280 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0261 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0035 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0357 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0157 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0339 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0274 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0254 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0346 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0315 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02080 | hp1 | a0001 | c0007 | t0001 | g0400 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02145 | hp1 | a0001 | c0018 | t0001 | g0395 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0288 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0323 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0391 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0326 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0370 | EAS | KHV | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0252 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0390 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0397 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0406 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0309 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0334 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0401 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0180 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0312 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0394 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0383 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0310 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0321 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0386 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0319 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0316 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0404 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0398 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0389 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0408 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0318 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0399 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0407 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0264 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0388 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0363 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0392 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03491 | hp2 | a0002 | c0006 | t0001 | g0005 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03492 | hp2 | a0002 | c0006 | t0001 | g0005 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0166 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0320 | AFR | ESN | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0306 | AFR | GWD | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0317 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0297 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0403 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0243 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0156 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0335 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03710 | hp2 | a0005 | c0010 | t0001 | g0304 | SAS | PJL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0361 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0179 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0134 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0298 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0355 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0373 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04184 | hp2 | a0006 | c0011 | t0001 | g0253 | SAS | BEB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0234 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | STU | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0325 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0338 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0285 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0322 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18961 | hp1 | a0001 | c0017 | t0001 | g0052 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0381 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0409 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0340 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19043 | hp2 | a0001 | c0007 | t0001 | g0272 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19060 | hp1 | a0007 | c0012 | t0001 | g0026 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0377 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0380 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0185 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA19240 | hp2 | a0001 | c0013 | t0001 | g0313 | AFR | YRI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0293 | AFR | ASW | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0387 | EUR | TSI | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0283 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02109 | hp2 | a0004 | c0015 | t0001 | g0410 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0405 | AFR | ACB | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | MSL | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0302 | AFR | USA | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18955 | hp1 | a0001 | c0016 | t0001 | g0232 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0303 | AFR | USA | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0393 | AFR | USA | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0382 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0396 | AFR | LWK | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0385 | REF | REF | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0117 | REF | REF | NPAS1_chr19_47014837_47050775 | NPAS1 | chr19 | 47014837 | 47050775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47032286 | C | T | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.367C>T | p.Arg123Cys | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 4/12 | 570/2100 | 367/1773 | 123/590 | chr19 | 47032286 | |||
| chr19:47039525 | G | A | 1 | a0003 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.923G>A | p.Arg308His | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/12 | 1126/2100 | 923/1773 | 308/590 | chr19 | 47039525 | |||
| chr19:47040488 | G | A | 1 | a0005 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1007G>A | p.Arg336His | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/12 | 1210/2100 | 1007/1773 | 336/590 | chr19 | 47040488 | |||
| chr19:47042832 | C | T | 1 | a0002 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1240C>T | p.Pro414Ser | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/12 | 1443/2100 | 1240/1773 | 414/590 | chr19 | 47042832 | |||
| chr19:47045472 | G | T | 1 | a0007 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1594G>T | p.Val532Leu | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 1797/2100 | 1594/1773 | 532/590 | chr19 | 47045472 | |||
| chr19:47045496 | G | A | 1 | a0006 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1618G>A | p.Gly540Ser | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 1821/2100 | 1618/1773 | 540/590 | chr19 | 47045496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47021137 | C | G | 3 | a0001c0004 a0001c0005 a0001c0008 |
19 | HG00642.hp2 HG01070.hp1 HG01243.hp2 others(16): Show |
synonymous_variant | LOW | c.90C>G | p.Pro30Pro | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/12 | 293/2100 | 90/1773 | 30/590 | chr19 | 47021137 | |||
| chr19:47021654 | C | T | 1 | a0001c0018 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.165C>T | p.Arg55Arg | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/12 | 368/2100 | 165/1773 | 55/590 | chr19 | 47021654 | |||
| chr19:47021795 | G | T | 2 | a0001c0016 a0001c0017 |
2 | NA18955.hp1 NA18961.hp1 |
synonymous_variant | LOW | c.306G>T | p.Ala102Ala | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/12 | 509/2100 | 306/1773 | 102/590 | chr19 | 47021795 | |||
| chr19:47040516 | G | A | 9 | a0001c0001 a0001c0003 a0001c0005 others(6): Show |
260 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(257): Show |
synonymous_variant | LOW | c.1035G>A | p.Gln345Gln | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/12 | 1238/2100 | 1035/1773 | 345/590 | chr19 | 47040516 | |||
| chr19:47040980 | C | T | 1 | a0001c0014 | 1 | HG00621.hp2 | splice_region_variant&synonymous_variant | LOW | c.1072C>T | p.Leu358Leu | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/12 | 1275/2100 | 1072/1773 | 358/590 | chr19 | 47040980 | |||
| chr19:47042900 | C | T | 1 | a0001c0013 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1308C>T | p.Pro436Pro | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/12 | 1511/2100 | 1308/1773 | 436/590 | chr19 | 47042900 | |||
| chr19:47045420 | G | A | 7 | a0001c0001 a0001c0005 a0001c0007 others(4): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
synonymous_variant | LOW | c.1542G>A | p.Ala514Ala | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 1745/2100 | 1542/1773 | 514/590 | chr19 | 47045420 | |||
| chr19:47045558 | T | C | 1 | a0007c0012 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.1680T>C | p.Gly560Gly | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 1883/2100 | 1680/1773 | 560/590 | chr19 | 47045558 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47021024 | C | A | 1 | a0001c0001t0003 | 3 | HG00408.hp2 NA18953.hp2 NA18971.hp1 |
5_prime_UTR_variant | MODIFIER | c.-24C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/12 | 24 | chr19 | 47021024 | ||||||
| chr19:47045703 | G | T | 1 | a0001c0001t0002 | 4 | HG00642.hp1 HG01168.hp2 HG01943.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*52G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 52 | chr19 | 47045703 | ||||||
| chr19:47045755 | C | T | 1 | a0001c0002t0004 | 2 | HG02717.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*104C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 12/12 | 104 | chr19 | 47045755 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:47020080 | A | C | 98 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0333 others(95): Show |
98 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-43+83A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020080 | |||||||
| chr19:47020084 | G | A | 1 | a0001c0002t0001g0009 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-43+87G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020084 | |||||||
| chr19:47020104 | C | G | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-43+107C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020104 | |||||||
| chr19:47020108 | C | A | 2 | a0001c0002t0001g0312 a0001c0013t0001g0313 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+111C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020108 | |||||||
| chr19:47020108 | C | G | 239 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0174 others(236): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.-43+111C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020108 | |||||||
| chr19:47020170 | C | G | 10 | a0001c0001t0001g0403 a0001c0001t0001g0405 a0001c0001t0001g0406 others(7): Show |
10 | HG00738.hp1 HG02080.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+173C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020170 | |||||||
| chr19:47020200 | C | G | 6 | a0001c0002t0001g0307 a0001c0002t0001g0308 a0001c0002t0001g0309 others(3): Show |
6 | HG01891.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+203C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020200 | |||||||
| chr19:47020239 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02698.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-43+242G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020239 | |||||||
| chr19:47020251 | G | C | 1 | a0001c0002t0001g0173 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-43+254G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020251 | |||||||
| chr19:47020326 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-43+329G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020326 | |||||||
| chr19:47020483 | G | A | 1 | a0001c0002t0001g0314 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-43+486G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020483 | |||||||
| chr19:47020502 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-42-504G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020502 | |||||||
| chr19:47020514 | T | C | 13 | a0001c0004t0001g0315 a0001c0004t0001g0316 a0001c0004t0001g0318 others(10): Show |
13 | HG00642.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42-492T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020514 | |||||||
| chr19:47020578 | G | A | 10 | a0001c0001t0001g0403 a0001c0001t0001g0405 a0001c0001t0001g0406 others(7): Show |
10 | HG00738.hp1 HG02080.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-42-428G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020578 | |||||||
| chr19:47020615 | C | T | 2 | a0001c0002t0001g0305 a0005c0010t0001g0304 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-42-391C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020615 | |||||||
| chr19:47020636 | C | A | 29 | a0001c0001t0001g0330 a0001c0001t0001g0332 a0001c0001t0001g0333 others(26): Show |
29 | HG01891.hp1 HG02027.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42-370C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020636 | |||||||
| chr19:47020644 | G | A | 1 | a0001c0002t0001g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-42-362G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020644 | |||||||
| chr19:47020894 | G | C | 1 | a0001c0001t0001g0021 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-42-112G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020894 | |||||||
| chr19:47020894 | G | GC | 82 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(79): Show |
83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-42-99dupC | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 47020894 | ||||||
| chr19:47020894 | G | GCC | 43 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0025 others(40): Show |
44 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-42-100_-42-99dupC others(1): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 47020894 | ||||||
| chr19:47020894 | GC | G | 54 | a0001c0001t0001g0054 a0001c0001t0001g0068 a0001c0001t0001g0105 others(51): Show |
54 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.-42-99delC | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 47020894 | ||||||
| chr19:47020894 | GCC | G | 135 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0174 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.-42-100_-42-99delC others(1): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 47020894 | ||||||
| chr19:47020894 | GCCC | G | 18 | a0001c0001t0001g0192 a0001c0001t0001g0259 a0001c0001t0001g0262 others(15): Show |
18 | HG00438.hp2 HG00741.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42-101_-42-99delC others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr19 | 47020894 | ||||||
| chr19:47020896 | C | A | 1 | a0001c0002t0001g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-42-110C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020896 | |||||||
| chr19:47020902 | C | A | 1 | a0001c0002t0001g0012 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-42-104C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020902 | |||||||
| chr19:47020980 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-42-26T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 1/11 | chr19 | 47020980 | |||||||
| chr19:47021182 | C | T | 1 | a0001c0001t0001g0409 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.122+13C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021182 | |||||||
| chr19:47021197 | C | T | 1 | a0001c0003t0001g0303 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.122+28C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021197 | |||||||
| chr19:47021199 | G | GA | 21 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0365 others(18): Show |
21 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+30_122+31insA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021199 | |||||||
| chr19:47021199 | G | GAC | 8 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(5): Show |
8 | HG00621.hp2 HG01433.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+30_122+31insAC | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021199 | |||||||
| chr19:47021200 | G | A | 4 | a0001c0001t0001g0384 a0001c0002t0001g0314 a0001c0002t0001g0386 others(1): Show |
4 | HG00280.hp1 HG01099.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+31G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021200 | |||||||
| chr19:47021200 | G | C | 29 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(26): Show |
29 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.122+31G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021200 | |||||||
| chr19:47021200 | G | GC | 25 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
25 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.122+40dupC | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr19 | 47021200 | ||||||
| chr19:47021201 | C | G | 2 | a0001c0002t0001g0310 a0001c0002t0001g0311 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122+32C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021201 | |||||||
| chr19:47021211 | G | A | 1 | a0001c0002t0001g0331 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+42G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021211 | |||||||
| chr19:47021349 | A | C | 10 | a0001c0001t0001g0403 a0001c0001t0001g0405 a0001c0001t0001g0406 others(7): Show |
10 | HG00738.hp1 HG02080.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+180A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021349 | |||||||
| chr19:47021353 | C | T | 2 | a0001c0004t0001g0302 a0001c0005t0001g0301 |
2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.122+184C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021353 | |||||||
| chr19:47021412 | C | A | 1 | a0001c0001t0001g0363 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.123-200C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 2/11 | chr19 | 47021412 | |||||||
| chr19:47022423 | C | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.358+576C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022423 | |||||||
| chr19:47022444 | G | GA | 4 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0332 others(1): Show |
4 | NA18988.hp2 NA18997.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+603dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47022444 | ||||||
| chr19:47022581 | G | A | 5 | a0001c0002t0001g0183 a0001c0002t0001g0184 a0001c0002t0001g0187 others(2): Show |
5 | HG02717.hp1 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+734G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022581 | |||||||
| chr19:47022674 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.358+827G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022674 | |||||||
| chr19:47022677 | T | C | 253 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.358+830T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022677 | |||||||
| chr19:47022678 | G | C | 260 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0025 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.358+831G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022678 | |||||||
| chr19:47022864 | G | A | 1 | a0001c0003t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.358+1017G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022864 | |||||||
| chr19:47022928 | A | T | 1 | a0001c0002t0001g0292 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.358+1081A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022928 | |||||||
| chr19:47022967 | C | T | 1 | a0001c0001t0001g0409 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.358+1120C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47022967 | |||||||
| chr19:47023197 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0171 a0001c0001t0001g0356 |
3 | NA18973.hp2 NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.358+1350A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023197 | |||||||
| chr19:47023266 | A | AG | 16 | a0001c0001t0001g0170 a0001c0001t0001g0286 a0001c0001t0001g0290 others(13): Show |
16 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+1426dupG | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47023266 | ||||||
| chr19:47023268 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.358+1421G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023268 | |||||||
| chr19:47023283 | G | A | 3 | a0001c0001t0001g0050 a0001c0002t0001g0024 a0001c0002t0001g0051 |
3 | HG00609.hp2 NA18959.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.358+1436G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023283 | |||||||
| chr19:47023450 | G | A | 2 | a0001c0001t0001g0333 a0001c0003t0001g0334 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.358+1603G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023450 | |||||||
| chr19:47023468 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.358+1621G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023468 | |||||||
| chr19:47023499 | C | A | 3 | a0001c0001t0001g0364 a0001c0002t0001g0294 a0001c0017t0001g0052 |
3 | HG00408.hp1 NA18961.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.358+1652C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023499 | |||||||
| chr19:47023512 | C | A | 1 | a0001c0002t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.358+1665C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023512 | |||||||
| chr19:47023543 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.358+1696G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023543 | |||||||
| chr19:47023594 | A | G | 1 | a0001c0001t0001g0406 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358+1747A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023594 | |||||||
| chr19:47023649 | T | C | 1 | a0001c0002t0001g0190 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.358+1802T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023649 | |||||||
| chr19:47023675 | G | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.358+1828G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023675 | |||||||
| chr19:47023751 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0365 |
2 | HG01975.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.358+1904G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023751 | |||||||
| chr19:47023769 | A | G | 175 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0037 others(172): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.358+1922A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023769 | |||||||
| chr19:47023826 | G | T | 7 | a0001c0001t0001g0143 a0001c0002t0001g0033 a0001c0002t0001g0142 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+1979G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023826 | |||||||
| chr19:47023827 | C | T | 7 | a0001c0001t0001g0143 a0001c0002t0001g0033 a0001c0002t0001g0142 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+1980C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023827 | |||||||
| chr19:47023917 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358+2070C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023917 | |||||||
| chr19:47023966 | G | A | 1 | a0001c0002t0001g0386 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.358+2119G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47023966 | |||||||
| chr19:47024007 | A | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
176 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.358+2160A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024007 | |||||||
| chr19:47024178 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358+2331T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024178 | |||||||
| chr19:47024201 | T | C | 1 | a0001c0002t0001g0057 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.358+2354T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024201 | |||||||
| chr19:47024378 | C | T | 1 | a0001c0002t0001g0382 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.358+2531C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024378 | |||||||
| chr19:47024379 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.358+2532G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024379 | |||||||
| chr19:47024480 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.358+2633C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024480 | |||||||
| chr19:47024499 | A | AAAC | 165 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.358+2667_358+2669d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024499 | ||||||
| chr19:47024538 | T | C | 1 | a0001c0007t0001g0400 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.358+2691T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024538 | |||||||
| chr19:47024652 | T | C | 378 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(375): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.358+2805T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024652 | |||||||
| chr19:47024678 | G | GTTCTAGG others(7): Show |
1 | a0001c0002t0001g0022 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.358+2832_358+2845d others(16): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024678 | ||||||
| chr19:47024698 | T | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0054 others(82): Show |
87 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.358+2851T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024698 | |||||||
| chr19:47024713 | C | T | 1 | a0001c0001t0001g0356 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.358+2866C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024713 | |||||||
| chr19:47024732 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0054 others(80): Show |
85 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.358+2885C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024732 | |||||||
| chr19:47024752 | T | C | 1 | a0001c0002t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358+2905T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024752 | |||||||
| chr19:47024809 | C | CT | 87 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.358+2979dupT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024809 | ||||||
| chr19:47024809 | C | CTT | 76 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0054 others(73): Show |
78 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.358+2978_358+2979d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024809 | ||||||
| chr19:47024809 | CT | C | 36 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0001t0001g0059 others(33): Show |
36 | HG01070.hp1 HG01243.hp2 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.358+2979delT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024809 | ||||||
| chr19:47024831 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(118): Show |
125 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.358+2984C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024831 | |||||||
| chr19:47024911 | G | A | 1 | a0001c0002t0001g0389 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.358+3064G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024911 | |||||||
| chr19:47024916 | TCTC | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.358+3072_358+3074d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47024916 | ||||||
| chr19:47024934 | C | T | 1 | a0001c0002t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.358+3087C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024934 | |||||||
| chr19:47024945 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0393 a0001c0002t0001g0208 others(3): Show |
6 | HG02055.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+3098G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024945 | |||||||
| chr19:47024955 | G | A | 2 | a0001c0002t0001g0305 a0005c0010t0001g0304 |
2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.358+3108G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024955 | |||||||
| chr19:47024964 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.358+3117C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024964 | |||||||
| chr19:47024973 | C | A | 1 | a0001c0002t0001g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.358+3126C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47024973 | |||||||
| chr19:47025008 | A | T | 46 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(44): Show |
intron_variant | MODIFIER | c.358+3161A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025008 | |||||||
| chr19:47025008 | ACCATGTT others(460): Show |
A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
126 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.358+3171_358+3637d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47025008 | ||||||
| chr19:47025070 | G | A | 1 | a0001c0002t0001g0382 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.358+3223G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025070 | |||||||
| chr19:47025071 | C | T | 4 | a0001c0001t0001g0028 a0001c0002t0001g0208 a0001c0002t0001g0329 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3224C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025071 | |||||||
| chr19:47025290 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358+3443T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025290 | |||||||
| chr19:47025296 | T | C | 49 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0050 others(46): Show |
49 | HG00639.hp1 HG02055.hp2 HG02056.hp2 others(46): Show |
intron_variant | MODIFIER | c.358+3449T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025296 | |||||||
| chr19:47025298 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358+3451G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025298 | |||||||
| chr19:47025340 | A | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0028 others(111): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.358+3493A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025340 | |||||||
| chr19:47025358 | A | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0330 |
2 | HG02135.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.358+3511A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025358 | |||||||
| chr19:47025371 | T | C | 2 | a0001c0004t0001g0302 a0001c0005t0001g0301 |
2 | HG01070.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.358+3524T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025371 | |||||||
| chr19:47025382 | G | A | 240 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.358+3535G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025382 | |||||||
| chr19:47025383 | A | G | 240 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.358+3536A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025383 | |||||||
| chr19:47025393 | T | C | 212 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.358+3546T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025393 | |||||||
| chr19:47025419 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0155 others(1): Show |
4 | HG00558.hp2 HG00597.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3572C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025419 | |||||||
| chr19:47025426 | G | T | 1 | a0001c0002t0001g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.358+3579G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025426 | |||||||
| chr19:47025428 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
9 | HG02083.hp1 NA18952.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+3581G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025428 | |||||||
| chr19:47025432 | C | G | 159 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(156): Show |
160 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.358+3585C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025432 | |||||||
| chr19:47025433 | C | T | 65 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0050 others(62): Show |
66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.358+3586C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025433 | |||||||
| chr19:47025435 | C | T | 1 | a0001c0002t0004g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+3588C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025435 | |||||||
| chr19:47025440 | A | G | 1 | a0001c0002t0004g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358+3593A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025440 | |||||||
| chr19:47025475 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18989.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.358+3628T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025475 | |||||||
| chr19:47025570 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
123 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.358+3723A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025570 | |||||||
| chr19:47025671 | G | A | 1 | a0001c0018t0001g0395 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.358+3824G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025671 | |||||||
| chr19:47025716 | C | G | 1 | a0001c0002t0004g0392 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+3869C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025716 | |||||||
| chr19:47025797 | A | G | 25 | a0001c0002t0001g0183 a0001c0002t0001g0209 a0001c0002t0001g0389 others(22): Show |
25 | HG01070.hp1 HG01243.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.358+3950A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025797 | |||||||
| chr19:47025807 | T | C | 1 | a0001c0002t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.358+3960T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025807 | |||||||
| chr19:47025824 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01069.hp2 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+3977C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025824 | |||||||
| chr19:47025872 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358+4025G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47025872 | |||||||
| chr19:47025949 | G | GT | 35 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0103 others(32): Show |
35 | HG00741.hp2 HG01515.hp2 HG01516.hp2 others(32): Show |
intron_variant | MODIFIER | c.358+4110dupT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47025949 | ||||||
| chr19:47026136 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.358+4289G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026136 | |||||||
| chr19:47026140 | C | T | 26 | a0001c0001t0001g0249 a0001c0001t0001g0265 a0001c0001t0001g0286 others(23): Show |
26 | HG00639.hp1 HG01070.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.358+4293C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026140 | |||||||
| chr19:47026150 | G | A | 24 | a0001c0001t0001g0333 a0001c0001t0001g0337 a0001c0002t0001g0110 others(21): Show |
24 | HG00642.hp2 HG01074.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.358+4303G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026150 | |||||||
| chr19:47026183 | T | C | 14 | a0001c0002t0001g0183 a0001c0002t0001g0258 a0001c0002t0001g0308 others(11): Show |
14 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.358+4336T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026183 | |||||||
| chr19:47026194 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.358+4347C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026194 | |||||||
| chr19:47026346 | G | A | 3 | a0001c0002t0001g0389 a0001c0002t0001g0391 a0001c0003t0001g0285 |
3 | HG02258.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.358+4499G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026346 | |||||||
| chr19:47026367 | T | C | 10 | a0001c0001t0001g0393 a0001c0002t0001g0029 a0001c0002t0001g0187 others(7): Show |
10 | HG01070.hp1 HG01070.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+4520T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026367 | |||||||
| chr19:47026387 | C | G | 69 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(66): Show |
71 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.358+4540C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026387 | |||||||
| chr19:47026406 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.358+4559G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026406 | |||||||
| chr19:47026483 | T | C | 125 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0020 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.358+4636T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026483 | |||||||
| chr19:47026484 | C | A | 1 | a0001c0004t0001g0315 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.358+4637C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026484 | |||||||
| chr19:47026547 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(48): Show |
53 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.358+4700T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026547 | |||||||
| chr19:47026646 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG00544.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.358+4799T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026646 | |||||||
| chr19:47026678 | G | A | 1 | a0001c0002t0004g0392 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+4831G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026678 | |||||||
| chr19:47026701 | T | C | 1 | a0001c0001t0001g0403 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.358+4854T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026701 | |||||||
| chr19:47026714 | T | G | 1 | a0001c0001t0001g0406 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358+4867T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026714 | |||||||
| chr19:47026803 | A | C | 1 | a0001c0002t0001g0408 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.358+4956A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026803 | |||||||
| chr19:47026816 | A | G | 3 | a0001c0001t0001g0143 a0001c0002t0001g0147 a0001c0002t0001g0209 |
3 | HG02572.hp1 HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.358+4969A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026816 | |||||||
| chr19:47026826 | T | TC | 165 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(162): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.358+4979_358+4980i others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026826 | |||||||
| chr19:47026834 | C | A | 355 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(352): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.358+4987C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026834 | |||||||
| chr19:47026871 | G | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(108): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.358+5024G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47026871 | |||||||
| chr19:47026952 | CA | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0300 others(8): Show |
11 | HG00733.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+5119delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47026952 | ||||||
| chr19:47027071 | G | A | 1 | a0001c0002t0001g0347 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.359-5207G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027071 | |||||||
| chr19:47027092 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.359-5186C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027092 | |||||||
| chr19:47027209 | G | C | 1 | a0001c0002t0001g0408 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.359-5069G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027209 | |||||||
| chr19:47027272 | C | T | 1 | a0001c0003t0001g0334 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.359-5006C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027272 | |||||||
| chr19:47027327 | T | TCCCCCTC others(15): Show |
72 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(69): Show |
74 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.359-4923_359-4902d others(24): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027327 | ||||||
| chr19:47027333 | T | TCTCTCTG others(14): Show |
129 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(126): Show |
134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.359-4944_359-4924d others(23): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027333 | ||||||
| chr19:47027350 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.359-4928C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027350 | |||||||
| chr19:47027413 | TG | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(81): Show |
85 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.359-4862delG | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027413 | ||||||
| chr19:47027444 | T | G | 1 | a0001c0002t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.359-4834T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027444 | |||||||
| chr19:47027448 | CTCTGCCC others(191): Show |
C | 5 | a0001c0001t0001g0393 a0001c0002t0001g0110 a0001c0002t0001g0269 others(2): Show |
5 | HG01433.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-4812_359-4615d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027448 | ||||||
| chr19:47027459 | G | T | 1 | a0001c0002t0001g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.359-4819G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027459 | |||||||
| chr19:47027462 | T | C | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4816T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027462 | |||||||
| chr19:47027463 | CCCGTCTC others(190): Show |
C | 1 | a0001c0002t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359-4812_359-4616d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027463 | ||||||
| chr19:47027465 | C | T | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4813C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027465 | |||||||
| chr19:47027466 | G | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(143): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.359-4812G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027466 | |||||||
| chr19:47027466 | GTCTCTCT others(103): Show |
G | 17 | a0001c0001t0001g0249 a0001c0002t0001g0111 a0001c0002t0001g0145 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.359-4768_359-4659d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027466 | ||||||
| chr19:47027480 | GGTCTCCC others(80): Show |
G | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-4796_359-4710d others(89): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027480 | ||||||
| chr19:47027487 | C | T | 2 | a0001c0002t0001g0183 a0001c0004t0001g0316 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.359-4791C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027487 | |||||||
| chr19:47027488 | G | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(80): Show |
84 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.359-4790G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027488 | |||||||
| chr19:47027492 | C | G | 2 | a0001c0002t0001g0183 a0001c0004t0001g0316 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.359-4786C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027492 | |||||||
| chr19:47027492 | CTCTGCCC others(147): Show |
C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(79): Show |
83 | HG00323.hp2 HG00423.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.359-4768_359-4615d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027492 | ||||||
| chr19:47027506 | TCCCATCT others(7): Show |
T | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4769_359-4756d others(16): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027506 | ||||||
| chr19:47027506 | TCCCATCT others(190): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.359-4768_359-4572d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027506 | ||||||
| chr19:47027509 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(198): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.359-4769C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027509 | |||||||
| chr19:47027510 | A | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(200): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.359-4768A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027510 | |||||||
| chr19:47027510 | A | T | 2 | a0001c0001t0001g0181 a0001c0002t0001g0207 |
2 | HG00140.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.359-4768A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027510 | |||||||
| chr19:47027514 | C | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(198): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.359-4764C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027514 | |||||||
| chr19:47027514 | CTCTGCCC others(125): Show |
C | 2 | a0001c0001t0001g0181 a0001c0002t0001g0207 |
2 | HG00140.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.359-4753_359-4622d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027514 | ||||||
| chr19:47027524 | GTTCTCCC others(1): Show |
G | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4752_359-4745d others(10): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027524 | ||||||
| chr19:47027525 | T | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(200): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.359-4753T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027525 | |||||||
| chr19:47027528 | TCCCTTCT others(168): Show |
T | 2 | a0001c0002t0001g0183 a0001c0004t0001g0316 |
2 | HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.359-4725_359-4551d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027528 | ||||||
| chr19:47027532 | T | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.359-4746T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027532 | |||||||
| chr19:47027536 | C | G | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4742C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027536 | |||||||
| chr19:47027536 | CTCTGCCC others(15): Show |
C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4725_359-4704d others(24): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027536 | ||||||
| chr19:47027550 | TCCTGTCT others(146): Show |
T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(142): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.359-4725_359-4573d others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027550 | ||||||
| chr19:47027576 | T | C | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-4702T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027576 | |||||||
| chr19:47027576 | T | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4702T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027576 | |||||||
| chr19:47027576 | TTCTCTCT others(37): Show |
T | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4676_359-4633d others(46): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027576 | ||||||
| chr19:47027591 | G | T | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-4687G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027591 | |||||||
| chr19:47027597 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4681C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027597 | |||||||
| chr19:47027598 | G | T | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-4680G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027598 | |||||||
| chr19:47027602 | C | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4676C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027602 | |||||||
| chr19:47027610 | CT | C | 3 | a0001c0001t0001g0260 a0001c0002t0001g0271 a0001c0003t0001g0261 |
3 | HG01261.hp1 HG02486.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.359-4667delT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027610 | |||||||
| chr19:47027619 | C | T | 73 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(70): Show |
75 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.359-4659C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027619 | |||||||
| chr19:47027624 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(70): Show |
75 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.359-4654C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027624 | |||||||
| chr19:47027624 | CTCTGCCC others(15): Show |
C | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-4636_359-4615d others(24): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47027624 | ||||||
| chr19:47027641 | C | T | 20 | a0001c0001t0001g0249 a0001c0001t0001g0406 a0001c0002t0001g0111 others(17): Show |
20 | HG00733.hp1 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.359-4637C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027641 | |||||||
| chr19:47027646 | G | C | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4632G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027646 | |||||||
| chr19:47027661 | C | T | 1 | a0001c0002t0001g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359-4617C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027661 | |||||||
| chr19:47027663 | C | T | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4615C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027663 | |||||||
| chr19:47027664 | T | G | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4614T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027664 | |||||||
| chr19:47027668 | C | G | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-4610C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027668 | |||||||
| chr19:47027703 | C | CT | 62 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(59): Show |
64 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.359-4575_359-4574i others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027703 | |||||||
| chr19:47027758 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.359-4520C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027758 | |||||||
| chr19:47027921 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.359-4357G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027921 | |||||||
| chr19:47027942 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0286 others(1): Show |
4 | HG00639.hp1 HG00738.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-4336C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47027942 | |||||||
| chr19:47028053 | G | T | 1 | a0001c0002t0001g0210 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.359-4225G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028053 | |||||||
| chr19:47028212 | G | A | 1 | a0001c0004t0001g0394 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.359-4066G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028212 | |||||||
| chr19:47028296 | C | G | 1 | a0001c0002t0001g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.359-3982C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028296 | |||||||
| chr19:47028330 | C | T | 1 | a0001c0001t0001g0359 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.359-3948C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028330 | |||||||
| chr19:47028701 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0195 a0001c0001t0001g0199 others(2): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-3577A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028701 | |||||||
| chr19:47028703 | C | T | 1 | a0001c0002t0001g0408 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.359-3575C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028703 | |||||||
| chr19:47028856 | C | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0262 a0001c0002t0001g0033 others(4): Show |
7 | HG01884.hp1 HG03225.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-3422C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028856 | |||||||
| chr19:47028925 | G | A | 1 | a0001c0003t0001g0297 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.359-3353G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028925 | |||||||
| chr19:47028937 | G | A | 8 | a0001c0002t0001g0145 a0001c0002t0001g0146 a0001c0002t0001g0165 others(5): Show |
8 | HG01243.hp2 HG02280.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-3341G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47028937 | |||||||
| chr19:47029042 | A | AT | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(115): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.359-3225dupT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47029042 | ||||||
| chr19:47029057 | TTTTG | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(75): Show |
79 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.359-3205_359-3202d others(6): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47029057 | ||||||
| chr19:47029058 | T | A | 1 | a0001c0002t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.359-3220T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029058 | |||||||
| chr19:47029059 | T | G | 1 | a0001c0002t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.359-3219T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029059 | |||||||
| chr19:47029061 | G | T | 1 | a0001c0002t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.359-3217G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029061 | |||||||
| chr19:47029153 | C | G | 4 | a0001c0002t0001g0118 a0001c0002t0001g0125 a0001c0002t0001g0131 others(1): Show |
4 | NA18953.hp1 NA19001.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-3125C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029153 | |||||||
| chr19:47029259 | G | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(217): Show |
227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.359-3019G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029259 | |||||||
| chr19:47029343 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0137 a0001c0002t0001g0116 others(2): Show |
6 | NA18952.hp1 NA18954.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-2935C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029343 | |||||||
| chr19:47029363 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | NA18747.hp1 NA18988.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.359-2915C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029363 | |||||||
| chr19:47029379 | C | T | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.359-2899C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029379 | |||||||
| chr19:47029396 | T | TTTA | 208 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(205): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.359-2864_359-2862d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47029396 | ||||||
| chr19:47029449 | G | A | 1 | a0001c0002t0001g0374 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.359-2829G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029449 | |||||||
| chr19:47029524 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.359-2754C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029524 | |||||||
| chr19:47029590 | A | G | 325 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(322): Show |
333 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.359-2688A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029590 | |||||||
| chr19:47029601 | ATGTTGGC others(16): Show |
A | 1 | a0001c0001t0001g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.359-2675_359-2653d others(25): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47029601 | ||||||
| chr19:47029653 | C | T | 3 | a0001c0001t0001g0406 a0001c0003t0001g0224 a0001c0003t0001g0306 |
3 | HG00733.hp1 HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.359-2625C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029653 | |||||||
| chr19:47029785 | C | T | 4 | a0001c0001t0001g0406 a0001c0002t0004g0186 a0001c0003t0001g0224 others(1): Show |
4 | HG00733.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2493C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029785 | |||||||
| chr19:47029864 | G | A | 1 | a0001c0018t0001g0395 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.359-2414G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029864 | |||||||
| chr19:47029952 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(145): Show |
153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.359-2326T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47029952 | |||||||
| chr19:47030167 | G | C | 1 | a0001c0003t0001g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.359-2111G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030167 | |||||||
| chr19:47030311 | G | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(220): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.359-1967G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030311 | |||||||
| chr19:47030337 | G | A | 1 | a0001c0002t0001g0213 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.359-1941G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030337 | |||||||
| chr19:47030401 | G | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(219): Show |
229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.359-1877G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030401 | |||||||
| chr19:47030568 | A | G | 2 | a0001c0002t0001g0390 a0001c0008t0001g0399 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.359-1710A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030568 | |||||||
| chr19:47030636 | C | CT | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0063 others(35): Show |
38 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.359-1611dupT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTT | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0084 a0001c0001t0001g0128 others(27): Show |
30 | HG00741.hp2 HG01175.hp2 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.359-1614_359-1611d others(6): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTT | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0050 others(58): Show |
62 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.359-1615_359-1611d others(7): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.359-1620_359-1611d others(12): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTTTT others(4): Show |
C | 7 | a0001c0001t0001g0137 a0001c0001t0001g0257 a0001c0001t0001g0354 others(4): Show |
7 | HG01981.hp1 HG02257.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-1621_359-1611d others(13): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTTTT others(5): Show |
C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0041 others(82): Show |
87 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.359-1622_359-1611d others(14): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTTTT others(6): Show |
C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(126): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.359-1623_359-1611d others(15): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030636 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0088 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.359-1624_359-1611d others(16): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47030636 | ||||||
| chr19:47030677 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(220): Show |
230 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.359-1601A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030677 | |||||||
| chr19:47030695 | C | G | 3 | a0001c0001t0001g0290 a0001c0002t0001g0210 a0001c0002t0001g0291 |
3 | HG00738.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.359-1583C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030695 | |||||||
| chr19:47030787 | G | A | 8 | a0001c0001t0001g0048 a0001c0001t0001g0195 a0001c0001t0001g0199 others(5): Show |
9 | HG01074.hp2 HG02698.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-1491G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47030787 | |||||||
| chr19:47031181 | T | TTG | 13 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0104 others(10): Show |
13 | HG00738.hp2 HG01167.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.359-1085_359-1084d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47031181 | ||||||
| chr19:47031193 | GT | G | 59 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(56): Show |
59 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.359-1065delT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47031193 | ||||||
| chr19:47031194 | T | TG | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(165): Show |
175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.359-1084_359-1083i others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031194 | |||||||
| chr19:47031195 | T | G | 141 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0021 others(138): Show |
142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.359-1083T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031195 | |||||||
| chr19:47031196 | T | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.359-1082T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031196 | |||||||
| chr19:47031197 | T | G | 12 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0048 others(9): Show |
12 | HG00738.hp2 HG01081.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-1081T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031197 | |||||||
| chr19:47031198 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0129 |
2 | HG01169.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.359-1080T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031198 | |||||||
| chr19:47031199 | T | G | 3 | a0001c0001t0001g0290 a0001c0002t0001g0210 a0001c0002t0001g0291 |
3 | HG00738.hp2 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.359-1079T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031199 | |||||||
| chr19:47031221 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.359-1057C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031221 | |||||||
| chr19:47031259 | C | T | 1 | a0001c0002t0001g0353 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.359-1019C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031259 | |||||||
| chr19:47031316 | G | A | 11 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0231 others(8): Show |
11 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-962G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031316 | |||||||
| chr19:47031483 | C | T | 143 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(140): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.359-795C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031483 | |||||||
| chr19:47031520 | CTTT | C | 310 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(307): Show |
318 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.359-754_359-752del others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47031520 | ||||||
| chr19:47031535 | CT | C | 299 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.359-730delT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr19 | 47031535 | ||||||
| chr19:47031782 | G | A | 1 | a0001c0002t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.359-496G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031782 | |||||||
| chr19:47031971 | C | G | 2 | a0001c0001t0001g0262 a0001c0005t0001g0325 |
2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.359-307C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47031971 | |||||||
| chr19:47032274 | C | G | 1 | a0001c0002t0001g0314 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.359-4C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 3/11 | chr19 | 47032274 | |||||||
| chr19:47032439 | A | G | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.432+88A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 4/11 | chr19 | 47032439 | |||||||
| chr19:47032444 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.432+93G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 4/11 | chr19 | 47032444 | |||||||
| chr19:47032537 | T | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(52): Show |
57 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.433-106T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 4/11 | chr19 | 47032537 | |||||||
| chr19:47032903 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.522+171A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47032903 | |||||||
| chr19:47032908 | T | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(148): Show |
156 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.522+176T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47032908 | |||||||
| chr19:47032962 | C | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0372 a0001c0002t0001g0118 others(3): Show |
6 | HG00438.hp1 NA18953.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.522+230C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47032962 | |||||||
| chr19:47033003 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(120): Show |
128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.522+271G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033003 | |||||||
| chr19:47033027 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0055 others(53): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.522+295C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033027 | |||||||
| chr19:47033097 | C | T | 1 | a0001c0001t0001g0375 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.522+365C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033097 | |||||||
| chr19:47033185 | C | T | 1 | a0001c0002t0001g0401 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.522+453C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033185 | |||||||
| chr19:47033241 | G | C | 15 | a0001c0001t0001g0249 a0001c0002t0001g0111 a0001c0002t0001g0145 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.522+509G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033241 | |||||||
| chr19:47033244 | A | AT | 67 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(64): Show |
67 | HG00408.hp2 HG00544.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.522+525dupT | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033244 | ||||||
| chr19:47033262 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.522+530T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033262 | |||||||
| chr19:47033390 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.522+658A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033390 | |||||||
| chr19:47033485 | G | A | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.522+753G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033485 | |||||||
| chr19:47033488 | T | C | 1 | a0001c0002t0001g0408 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.522+756T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033488 | |||||||
| chr19:47033726 | GC | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0062 others(2): Show |
5 | HG00597.hp1 HG01069.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+996delC | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033726 | ||||||
| chr19:47033821 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.522+1089A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47033821 | |||||||
| chr19:47033975 | T | TA | 8 | a0001c0001t0001g0037 a0001c0001t0001g0172 a0001c0001t0001g0359 others(5): Show |
8 | HG01106.hp1 HG01517.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+1289dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TA | T | 16 | a0001c0001t0001g0098 a0001c0001t0001g0214 a0001c0001t0001g0299 others(13): Show |
16 | HG00673.hp2 HG01069.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.522+1289delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAA | T | 9 | a0001c0001t0001g0182 a0001c0001t0001g0300 a0001c0001t0001g0356 others(6): Show |
9 | HG00621.hp2 HG01169.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+1288_522+1289d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAA | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
14 | HG00408.hp2 HG00741.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.522+1287_522+1289d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAA | T | 8 | a0001c0001t0001g0202 a0001c0001t0001g0222 a0001c0001t0001g0238 others(5): Show |
8 | HG01981.hp1 HG02015.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+1286_522+1289d others(6): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAA | T | 16 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0354 others(13): Show |
16 | HG00609.hp2 HG01884.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.522+1285_522+1289d others(7): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAA | T | 8 | a0001c0001t0001g0055 a0001c0002t0001g0226 a0001c0002t0001g0401 others(5): Show |
8 | HG01261.hp1 HG01975.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+1284_522+1289d others(8): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0332 |
2 | NA19012.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.522+1280_522+1289d others(12): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(7): Show |
T | 1 | a0001c0003t0001g0278 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.522+1276_522+1289d others(16): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0001g0393 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.522+1275_522+1289d others(17): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(9): Show |
T | 5 | a0001c0001t0001g0235 a0001c0002t0001g0110 a0001c0002t0001g0268 others(2): Show |
5 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.522+1274_522+1289d others(18): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(10): Show |
T | 1 | a0001c0002t0001g0357 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.522+1273_522+1289d others(19): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(11): Show |
T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | NA18964.hp2 NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.522+1272_522+1289d others(20): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(12): Show |
T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0405 a0001c0002t0001g0061 others(5): Show |
8 | HG01175.hp2 HG02559.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.522+1271_522+1289d others(21): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(13): Show |
T | 21 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0231 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.522+1270_522+1289d others(22): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(14): Show |
T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0076 others(13): Show |
17 | HG00280.hp1 HG00673.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.522+1269_522+1289d others(23): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(15): Show |
T | 1 | a0001c0002t0001g0140 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.522+1268_522+1289d others(24): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(18): Show |
T | 3 | a0001c0002t0001g0389 a0001c0002t0001g0391 a0001c0003t0001g0264 |
3 | HG02258.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.522+1265_522+1289d others(27): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(19): Show |
T | 1 | a0001c0003t0001g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.522+1264_522+1289d others(28): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(21): Show |
T | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.522+1262_522+1289d others(30): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(23): Show |
T | 6 | a0001c0001t0001g0094 a0001c0001t0001g0128 a0001c0001t0001g0178 others(3): Show |
7 | HG01255.hp1 HG01496.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+1260_522+1289d others(32): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(24): Show |
T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
220 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.522+1259_522+1289d others(33): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47033975 | TAAAAAAA others(25): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.522+1258_522+1289d others(34): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47033975 | ||||||
| chr19:47034021 | A | G | 1 | a0001c0002t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.522+1289A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034021 | |||||||
| chr19:47034024 | G | C | 1 | a0001c0002t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.522+1292G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034024 | |||||||
| chr19:47034043 | G | A | 1 | a0001c0002t0004g0392 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.522+1311G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034043 | |||||||
| chr19:47034103 | AAGACCAG others(870): Show |
A | 1 | a0001c0002t0001g0247 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.522+1406_523-950de others(1): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47034103 | ||||||
| chr19:47034207 | G | A | 9 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0231 others(6): Show |
9 | HG00140.hp2 HG00323.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+1475G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034207 | |||||||
| chr19:47034256 | G | A | 1 | a0001c0002t0001g0116 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.522+1524G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034256 | |||||||
| chr19:47034314 | C | CA | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
230 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.522+1601dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47034314 | ||||||
| chr19:47034314 | C | CAA | 7 | a0001c0001t0001g0078 a0001c0001t0001g0130 a0001c0001t0001g0178 others(4): Show |
7 | HG02135.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.522+1600_522+1601d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47034314 | ||||||
| chr19:47034335 | G | T | 1 | a0001c0002t0001g0361 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.522+1603G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034335 | |||||||
| chr19:47034365 | T | C | 10 | a0001c0001t0001g0143 a0001c0002t0001g0147 a0001c0002t0001g0209 others(7): Show |
10 | HG01074.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.523-1599T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034365 | |||||||
| chr19:47034373 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.523-1591T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034373 | |||||||
| chr19:47034522 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0276 a0001c0001t0001g0281 others(1): Show |
4 | HG01123.hp2 HG01952.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-1442G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034522 | |||||||
| chr19:47034698 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0163 |
4 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-1266G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034698 | |||||||
| chr19:47034770 | A | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(257): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.523-1194A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034770 | |||||||
| chr19:47034837 | T | C | 33 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0075 others(30): Show |
34 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.523-1127T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034837 | |||||||
| chr19:47034923 | C | T | 34 | a0001c0001t0001g0058 a0001c0001t0001g0076 a0001c0001t0001g0100 others(31): Show |
34 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.523-1041C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47034923 | |||||||
| chr19:47034937 | TTTGGGAG others(127): Show |
T | 1 | a0001c0002t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.523-1017_523-884de others(1): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47034937 | ||||||
| chr19:47035097 | C | T | 1 | a0001c0002t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.523-867C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035097 | |||||||
| chr19:47035165 | G | A | 6 | a0001c0001t0001g0143 a0001c0002t0001g0147 a0001c0002t0001g0183 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.523-799G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035165 | |||||||
| chr19:47035191 | A | AAAG | 17 | a0001c0001t0001g0048 a0001c0001t0001g0195 a0001c0001t0001g0199 others(14): Show |
18 | HG01099.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-745_523-743dup others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAG | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(128): Show |
133 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.523-748_523-743dup others(6): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(2): Show |
52 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0044 others(49): Show |
53 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.523-751_523-743dup others(9): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(5): Show |
25 | a0001c0001t0001g0021 a0001c0001t0001g0058 a0001c0001t0001g0078 others(22): Show |
25 | HG00280.hp1 HG00673.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.523-754_523-743dup others(12): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(8): Show |
18 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0164 others(15): Show |
18 | HG00558.hp1 HG01070.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.523-757_523-743dup others(15): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(11): Show |
14 | a0001c0001t0001g0076 a0001c0001t0001g0098 a0001c0001t0001g0102 others(11): Show |
15 | HG01069.hp2 HG01167.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-760_523-743dup others(18): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(14): Show |
2 | a0001c0001t0001g0364 a0001c0002t0001g0401 |
2 | HG00408.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.523-763_523-743dup others(21): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(29): Show |
1 | a0001c0004t0001g0394 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.523-743_523-742ins others(36): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | A | AAAGAAGA others(47): Show |
1 | a0001c0002t0001g0408 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.523-743_523-742ins others(54): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035191 | AAAG | A | 106 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(103): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.523-745_523-743del others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr19 | 47035191 | ||||||
| chr19:47035370 | G | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
47 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.523-594G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035370 | |||||||
| chr19:47035454 | T | C | 1 | a0001c0002t0001g0204 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.523-510T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035454 | |||||||
| chr19:47035678 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.523-286G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035678 | |||||||
| chr19:47035772 | G | A | 3 | a0001c0001t0001g0345 a0001c0002t0001g0331 a0001c0002t0001g0342 |
3 | NA18940.hp2 NA18968.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.523-192G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035772 | |||||||
| chr19:47035827 | T | A | 1 | a0001c0002t0001g0340 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.523-137T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 5/11 | chr19 | 47035827 | |||||||
| chr19:47036313 | A | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG02015.hp1 HG02027.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.688+184A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036313 | |||||||
| chr19:47036314 | A | G | 148 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(145): Show |
152 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.688+185A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036314 | |||||||
| chr19:47036322 | A | G | 1 | a0001c0003t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.688+193A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036322 | |||||||
| chr19:47036423 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.688+294C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036423 | |||||||
| chr19:47036432 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.688+303C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036432 | |||||||
| chr19:47036471 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.688+342C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036471 | |||||||
| chr19:47036701 | ATC | A | 71 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0065 others(68): Show |
72 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.688+576_688+577del others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47036701 | ||||||
| chr19:47036717 | C | CA | 21 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0143 others(18): Show |
22 | HG00741.hp1 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.688+604dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47036717 | ||||||
| chr19:47036717 | C | CAA | 65 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(62): Show |
65 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.688+603_688+604dup others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47036717 | ||||||
| chr19:47036717 | C | CAAA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0028 others(6): Show |
9 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+602_688+604dup others(3): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47036717 | ||||||
| chr19:47036717 | CA | C | 83 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0065 others(80): Show |
84 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.688+604delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47036717 | ||||||
| chr19:47036806 | C | G | 1 | a0001c0003t0001g0236 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.688+677C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036806 | |||||||
| chr19:47036811 | G | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(72): Show |
76 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.688+682G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036811 | |||||||
| chr19:47036893 | C | A | 1 | a0001c0002t0001g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.688+764C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036893 | |||||||
| chr19:47036963 | T | C | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(72): Show |
76 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.688+834T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036963 | |||||||
| chr19:47036973 | G | T | 1 | a0001c0003t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.688+844G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47036973 | |||||||
| chr19:47037039 | G | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(72): Show |
76 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.688+910G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037039 | |||||||
| chr19:47037052 | G | GA | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.688+940dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037052 | ||||||
| chr19:47037052 | G | GAA | 31 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0084 others(28): Show |
31 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.688+939_688+940dup others(2): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037052 | ||||||
| chr19:47037070 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.688+941G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037070 | |||||||
| chr19:47037133 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0218 |
2 | HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.688+1004C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037133 | |||||||
| chr19:47037209 | G | A | 2 | a0001c0001t0001g0181 a0001c0003t0001g0297 |
2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.688+1080G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037209 | |||||||
| chr19:47037265 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0356 |
2 | NA18973.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.688+1136C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037265 | |||||||
| chr19:47037299 | C | T | 1 | a0001c0001t0001g0376 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.688+1170C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037299 | |||||||
| chr19:47037338 | C | CA | 90 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0050 others(87): Show |
91 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.688+1239dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | C | CAA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0350 a0001c0002t0001g0051 others(11): Show |
14 | HG00609.hp2 HG02109.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.688+1238_688+1239d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | C | CAAA | 16 | a0001c0001t0001g0143 a0001c0001t0002g0273 a0001c0002t0001g0147 others(13): Show |
16 | HG00738.hp2 HG02027.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.688+1237_688+1239d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CA | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0120 others(18): Show |
21 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.688+1239delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAA | C | 9 | a0001c0001t0001g0375 a0001c0002t0001g0110 a0001c0002t0001g0268 others(6): Show |
9 | HG02015.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.688+1238_688+1239d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAAA | C | 6 | a0001c0002t0001g0207 a0001c0002t0001g0209 a0001c0002t0001g0269 others(3): Show |
6 | HG01074.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+1237_688+1239d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAAAAAA | C | 19 | a0001c0001t0001g0102 a0001c0002t0001g0187 a0001c0002t0001g0335 others(16): Show |
19 | HG00733.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.688+1234_688+1239d others(8): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAAAAAAA | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(49): Show |
53 | HG00323.hp2 HG00738.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.688+1233_688+1239d others(9): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0062 others(10): Show |
13 | HG00597.hp1 HG01109.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.688+1229_688+1239d others(13): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037338 | CAAAAAAA others(6): Show |
C | 2 | a0001c0003t0001g0261 a0001c0004t0001g0388 |
2 | HG01261.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.688+1227_688+1239d others(15): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037338 | ||||||
| chr19:47037360 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.688+1231A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037360 | |||||||
| chr19:47037478 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0189 others(2): Show |
5 | NA18950.hp2 NA18962.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.688+1349C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037478 | |||||||
| chr19:47037486 | TA | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0114 |
3 | NA18952.hp2 NA19085.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.688+1359delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47037486 | ||||||
| chr19:47037508 | G | A | 1 | a0001c0001t0001g0380 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.688+1379G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037508 | |||||||
| chr19:47037575 | C | G | 1 | a0001c0003t0001g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.688+1446C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037575 | |||||||
| chr19:47037743 | A | T | 71 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0037 others(68): Show |
72 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.689-1293A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037743 | |||||||
| chr19:47037918 | C | G | 16 | a0001c0001t0001g0249 a0001c0001t0001g0265 a0001c0001t0001g0406 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.689-1118C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47037918 | |||||||
| chr19:47038196 | G | A | 1 | a0001c0002t0001g0348 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.689-840G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038196 | |||||||
| chr19:47038247 | A | G | 1 | a0001c0002t0001g0369 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.689-789A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038247 | |||||||
| chr19:47038285 | G | C | 11 | a0001c0002t0001g0033 a0001c0002t0001g0207 a0001c0002t0001g0209 others(8): Show |
11 | HG01074.hp1 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.689-751G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038285 | |||||||
| chr19:47038289 | C | T | 1 | a0001c0002t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.689-747C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038289 | |||||||
| chr19:47038314 | T | G | 1 | a0001c0003t0001g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.689-722T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038314 | |||||||
| chr19:47038329 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.689-707C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038329 | |||||||
| chr19:47038337 | C | T | 2 | a0001c0001t0001g0378 a0001c0002t0001g0051 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.689-699C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038337 | |||||||
| chr19:47038340 | T | A | 1 | a0001c0002t0001g0051 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.689-696T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038340 | |||||||
| chr19:47038379 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.689-657T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038379 | |||||||
| chr19:47038385 | C | T | 20 | a0001c0002t0001g0142 a0001c0002t0001g0165 a0001c0002t0001g0184 others(17): Show |
20 | HG01891.hp2 HG01934.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.689-651C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038385 | |||||||
| chr19:47038386 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.689-650G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038386 | |||||||
| chr19:47038420 | G | A | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.689-616G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038420 | |||||||
| chr19:47038454 | T | TCGCAGTA others(21): Show |
119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(116): Show |
122 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.689-580_689-553dup others(28): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47038454 | ||||||
| chr19:47038460 | T | G | 1 | a0001c0002t0004g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.689-576T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038460 | |||||||
| chr19:47038472 | G | GTGCCACT others(21): Show |
2 | a0001c0001t0001g0189 a0001c0001t0001g0217 |
2 | NA18962.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.689-553_689-552ins others(28): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47038472 | ||||||
| chr19:47038515 | C | CA | 14 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0084 others(11): Show |
14 | HG01106.hp2 HG01255.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.689-503dupA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47038515 | ||||||
| chr19:47038515 | CA | C | 38 | a0001c0001t0001g0171 a0001c0001t0001g0230 a0001c0002t0001g0033 others(35): Show |
38 | HG00323.hp2 HG01074.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.689-503delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr19 | 47038515 | ||||||
| chr19:47038574 | C | T | 119 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0062 others(116): Show |
120 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.689-462C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038574 | |||||||
| chr19:47038660 | C | G | 6 | a0001c0002t0001g0226 a0001c0003t0001g0031 a0001c0003t0001g0032 others(3): Show |
6 | HG02602.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.689-376C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038660 | |||||||
| chr19:47038775 | C | T | 5 | a0001c0002t0001g0183 a0001c0002t0001g0187 a0001c0002t0001g0291 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-261C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038775 | |||||||
| chr19:47038776 | A | G | 5 | a0001c0002t0001g0183 a0001c0002t0001g0187 a0001c0002t0001g0291 others(2): Show |
5 | HG02055.hp1 HG02615.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.689-260A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038776 | |||||||
| chr19:47038802 | G | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(229): Show |
239 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.689-234G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038802 | |||||||
| chr19:47038820 | A | G | 7 | a0001c0001t0001g0260 a0001c0002t0001g0147 a0001c0002t0001g0329 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.689-216A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038820 | |||||||
| chr19:47038846 | C | A | 1 | a0001c0001t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.689-190C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038846 | |||||||
| chr19:47038891 | T | A | 1 | a0004c0015t0001g0410 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.689-145T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038891 | |||||||
| chr19:47038921 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.689-115C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038921 | |||||||
| chr19:47038956 | C | T | 1 | a0001c0002t0001g0305 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.689-80C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038956 | |||||||
| chr19:47038957 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.689-79G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 6/11 | chr19 | 47038957 | |||||||
| chr19:47039167 | C | T | 19 | a0001c0003t0001g0001 a0001c0003t0001g0035 a0001c0003t0001g0049 others(16): Show |
20 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.804+16C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 7/11 | chr19 | 47039167 | |||||||
| chr19:47039275 | G | A | 1 | a0001c0013t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804+124G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 7/11 | chr19 | 47039275 | |||||||
| chr19:47039358 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.805-49C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 7/11 | chr19 | 47039358 | |||||||
| chr19:47039370 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.805-37G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 7/11 | chr19 | 47039370 | |||||||
| chr19:47039570 | G | A | 1 | a0001c0002t0001g0074 | 1 | HG01928.hp2 | splice_region_variant&intron_variant | LOW | c.962+6G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47039570 | |||||||
| chr19:47039745 | G | A | 3 | a0001c0001t0001g0376 a0001c0002t0001g0289 a0001c0004t0001g0323 |
3 | HG02145.hp2 HG02258.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.962+181G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47039745 | |||||||
| chr19:47039801 | G | A | 1 | a0001c0002t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.962+237G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47039801 | |||||||
| chr19:47039850 | T | TTCTCATT others(16): Show |
34 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0019 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.962+293_962+315dup others(23): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr19 | 47039850 | ||||||
| chr19:47039875 | C | CTCATTTC others(17): Show |
1 | a0007c0012t0001g0026 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.962+315_962+316ins others(24): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr19 | 47039875 | ||||||
| chr19:47039909 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.962+345G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47039909 | |||||||
| chr19:47039983 | G | A | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(253): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.962+419G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47039983 | |||||||
| chr19:47040046 | A | G | 3 | a0001c0002t0001g0147 a0001c0002t0001g0329 a0001c0004t0001g0394 |
3 | HG02572.hp1 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.963-398A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 8/11 | chr19 | 47040046 | |||||||
| chr19:47040738 | T | TG | 43 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0037 others(40): Show |
43 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1069+198dupG | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr19 | 47040738 | ||||||
| chr19:47040740 | G | T | 133 | a0001c0001t0001g0113 a0001c0001t0001g0122 a0001c0002t0001g0002 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1069+190G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | chr19 | 47040740 | |||||||
| chr19:47040742 | G | T | 42 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0019 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1069+192G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | chr19 | 47040742 | |||||||
| chr19:47040876 | C | G | 3 | a0001c0002t0001g0040 a0001c0002t0001g0175 a0001c0002t0001g0203 |
3 | HG01358.hp1 HG01496.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1070-102C>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | chr19 | 47040876 | |||||||
| chr19:47040931 | C | T | 4 | a0001c0002t0001g0147 a0001c0002t0001g0329 a0001c0002t0004g0392 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-47C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | chr19 | 47040931 | |||||||
| chr19:47040938 | C | A | 2 | a0001c0002t0001g0111 a0001c0002t0001g0271 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1070-40C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 9/11 | chr19 | 47040938 | |||||||
| chr19:47041295 | C | T | 2 | a0001c0002t0001g0111 a0001c0002t0001g0271 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1217+170C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041295 | |||||||
| chr19:47041296 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1217+171G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041296 | |||||||
| chr19:47041359 | G | T | 1 | a0001c0001t0001g0372 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1217+234G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041359 | |||||||
| chr19:47041435 | G | A | 4 | a0001c0002t0001g0207 a0001c0002t0001g0266 a0001c0002t0001g0307 others(1): Show |
4 | HG01891.hp2 HG01934.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+310G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041435 | |||||||
| chr19:47041633 | A | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0077 others(1): Show |
4 | NA18946.hp1 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1217+508A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041633 | |||||||
| chr19:47041693 | G | A | 7 | a0001c0002t0001g0030 a0001c0002t0001g0057 a0001c0002t0001g0074 others(4): Show |
7 | HG01928.hp2 NA18953.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.1217+568G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041693 | |||||||
| chr19:47041770 | C | T | 379 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(376): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1217+645C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041770 | |||||||
| chr19:47041791 | C | A | 131 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1217+666C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041791 | |||||||
| chr19:47041821 | A | T | 125 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(122): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1217+696A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041821 | |||||||
| chr19:47041822 | T | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(251): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1217+697T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041822 | |||||||
| chr19:47041828 | T | A | 379 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(376): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1217+703T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041828 | |||||||
| chr19:47041945 | T | A | 383 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(380): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1217+820T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041945 | |||||||
| chr19:47041959 | G | A | 2 | a0001c0002t0001g0111 a0001c0002t0001g0271 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1217+834G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47041959 | |||||||
| chr19:47041979 | CA | C | 7 | a0001c0002t0001g0147 a0001c0002t0001g0328 a0001c0002t0001g0329 others(4): Show |
7 | HG02109.hp1 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-803delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47041979 | ||||||
| chr19:47041979 | CAAAAAAA | C | 6 | a0001c0002t0001g0002 a0001c0002t0001g0033 a0001c0002t0001g0183 others(3): Show |
7 | HG01516.hp1 HG01517.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-809_1218-803d others(9): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47041979 | ||||||
| chr19:47041979 | CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0084 others(9): Show |
12 | HG01123.hp2 HG01243.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1218-813_1218-803d others(13): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47041979 | ||||||
| chr19:47041979 | CAAAAAAA others(5): Show |
C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(239): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1218-814_1218-803d others(14): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47041979 | ||||||
| chr19:47042007 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0104 others(3): Show |
6 | HG01243.hp1 HG01517.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218-803A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042007 | |||||||
| chr19:47042008 | G | A | 31 | a0001c0002t0001g0024 a0001c0002t0001g0027 a0001c0002t0001g0029 others(28): Show |
31 | HG00609.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1218-802G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042008 | |||||||
| chr19:47042009 | G | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0068 a0001c0001t0001g0104 others(7): Show |
10 | HG00741.hp2 HG01070.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1218-801G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042009 | |||||||
| chr19:47042009 | GA | G | 25 | a0001c0002t0001g0024 a0001c0002t0001g0027 a0001c0002t0001g0053 others(22): Show |
25 | HG00609.hp1 HG00735.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1218-795delA | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47042009 | ||||||
| chr19:47042009 | GAA | G | 90 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1218-796_1218-795d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47042009 | ||||||
| chr19:47042010 | A | G | 1 | a0001c0004t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1218-800A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042010 | |||||||
| chr19:47042011 | A | AAAAGG | 3 | a0001c0002t0001g0029 a0001c0002t0001g0355 a0001c0002t0001g0404 |
3 | HG01070.hp2 HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1218-796_1218-795i others(7): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr19 | 47042011 | ||||||
| chr19:47042011 | A | G | 26 | a0001c0002t0001g0024 a0001c0002t0001g0027 a0001c0002t0001g0053 others(23): Show |
26 | HG00609.hp1 HG00735.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218-799A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042011 | |||||||
| chr19:47042015 | A | T | 1 | a0001c0002t0001g0191 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1218-795A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042015 | |||||||
| chr19:47042046 | G | A | 1 | a0001c0002t0001g0369 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1218-764G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042046 | |||||||
| chr19:47042083 | G | A | 4 | a0001c0002t0001g0328 a0001c0002t0004g0186 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp1 HG02109.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-727G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042083 | |||||||
| chr19:47042152 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1218-658A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042152 | |||||||
| chr19:47042191 | C | T | 123 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1218-619C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042191 | |||||||
| chr19:47042330 | A | C | 4 | a0001c0002t0001g0147 a0001c0002t0001g0329 a0001c0002t0004g0392 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1218-480A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042330 | |||||||
| chr19:47042333 | A | G | 2 | a0001c0003t0001g0167 a0001c0003t0001g0334 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1218-477A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042333 | |||||||
| chr19:47042402 | G | C | 1 | a0001c0013t0001g0313 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1218-408G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042402 | |||||||
| chr19:47042430 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1218-380A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042430 | |||||||
| chr19:47042453 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1218-357A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042453 | |||||||
| chr19:47042461 | C | T | 383 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(380): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.1218-349C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042461 | |||||||
| chr19:47042644 | A | C | 3 | a0001c0002t0001g0147 a0001c0002t0001g0329 a0001c0004t0001g0394 |
3 | HG02572.hp1 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1218-166A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042644 | |||||||
| chr19:47042685 | T | C | 45 | a0001c0002t0001g0009 a0001c0002t0001g0017 a0001c0002t0001g0019 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.1218-125T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042685 | |||||||
| chr19:47042768 | C | T | 2 | a0001c0002t0001g0340 a0001c0004t0001g0302 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1218-42C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 10/11 | chr19 | 47042768 | |||||||
| chr19:47043089 | G | A | 2 | a0001c0002t0001g0111 a0001c0002t0001g0271 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1312+185G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043089 | |||||||
| chr19:47043152 | T | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0249 a0001c0001t0001g0262 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312+248T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043152 | |||||||
| chr19:47043169 | G | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+265G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043169 | |||||||
| chr19:47043278 | C | CAAAAAAA | 17 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0090 others(14): Show |
17 | HG00140.hp1 HG00323.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1312+387_1312+393d others(9): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | C | CAAAAAAA others(1): Show |
209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(206): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1312+386_1312+393d others(10): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | C | CAAAAAAA others(2): Show |
65 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0020 others(62): Show |
67 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1312+385_1312+393d others(11): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | C | CAAAAAAA others(3): Show |
39 | a0001c0001t0001g0077 a0001c0001t0001g0199 a0001c0001t0001g0366 others(36): Show |
39 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1312+384_1312+393d others(12): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | C | CAAAAAAA others(4): Show |
8 | a0001c0003t0001g0135 a0001c0003t0001g0156 a0001c0003t0001g0254 others(5): Show |
8 | HG01258.hp1 HG01928.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+383_1312+393d others(13): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | C | CAAAAAAA others(5): Show |
6 | a0001c0002t0001g0187 a0001c0003t0001g0211 a0001c0003t0001g0283 others(3): Show |
6 | HG00642.hp2 HG01123.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312+382_1312+393d others(14): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043278 | CAAA | C | 8 | a0001c0002t0001g0147 a0001c0002t0001g0207 a0001c0002t0001g0266 others(5): Show |
8 | HG01891.hp2 HG01934.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+391_1312+393d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043278 | ||||||
| chr19:47043315 | A | C | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+411A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043315 | |||||||
| chr19:47043332 | G | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+428G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043332 | |||||||
| chr19:47043440 | A | T | 1 | a0001c0001t0001g0407 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1312+536A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043440 | |||||||
| chr19:47043539 | G | A | 379 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(376): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.1312+635G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043539 | |||||||
| chr19:47043553 | G | A | 4 | a0001c0002t0001g0207 a0001c0002t0001g0266 a0001c0002t0001g0307 others(1): Show |
4 | HG01891.hp2 HG01934.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+649G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043553 | |||||||
| chr19:47043562 | T | C | 12 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0001g0207 others(9): Show |
12 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312+658T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043562 | |||||||
| chr19:47043594 | AAAC | A | 12 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0001g0207 others(9): Show |
12 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1312+693_1312+695d others(5): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043594 | ||||||
| chr19:47043671 | C | T | 1 | a0001c0003t0001g0303 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1312+767C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043671 | |||||||
| chr19:47043716 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1312+812C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043716 | |||||||
| chr19:47043759 | A | AAAAAT | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312+871_1312+875d others(7): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043759 | ||||||
| chr19:47043759 | AAAAAT | A | 8 | a0001c0002t0001g0147 a0001c0002t0001g0207 a0001c0002t0001g0266 others(5): Show |
8 | HG01891.hp2 HG01934.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+871_1312+875d others(7): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043759 | ||||||
| chr19:47043787 | C | A | 8 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0001g0271 others(5): Show |
8 | HG02109.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+883C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043787 | |||||||
| chr19:47043788 | G | C | 1 | a0001c0001t0001g0170 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1312+884G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043788 | |||||||
| chr19:47043840 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1312+936G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043840 | |||||||
| chr19:47043865 | GACAAGCC others(27): Show |
G | 1 | a0001c0001t0001g0129 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1312+966_1312+999d others(36): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47043865 | ||||||
| chr19:47043896 | C | A | 1 | a0001c0003t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1312+992C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043896 | |||||||
| chr19:47043959 | G | A | 1 | a0001c0001t0001g0366 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1312+1055G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043959 | |||||||
| chr19:47043990 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1312+1086C>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47043990 | |||||||
| chr19:47044071 | A | AATTT | 12 | a0001c0002t0001g0111 a0001c0002t0001g0147 a0001c0002t0001g0207 others(9): Show |
12 | HG01891.hp2 HG01934.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1313-1111_1313-110 others(8): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47044071 | ||||||
| chr19:47044170 | T | G | 1 | a0007c0012t0001g0026 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1313-1021T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044170 | |||||||
| chr19:47044355 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1313-836G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044355 | |||||||
| chr19:47044386 | C | CAA | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(212): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1313-800_1313-799d others(4): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47044386 | ||||||
| chr19:47044415 | T | C | 1 | a0001c0002t0001g0338 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1313-776T>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044415 | |||||||
| chr19:47044435 | A | G | 396 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(393): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1313-756A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044435 | |||||||
| chr19:47044507 | A | C | 1 | a0001c0003t0001g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1313-684A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044507 | |||||||
| chr19:47044591 | G | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-600G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044591 | |||||||
| chr19:47044606 | G | T | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-585G>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044606 | |||||||
| chr19:47044608 | T | G | 1 | a0007c0012t0001g0026 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1313-583T>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044608 | |||||||
| chr19:47044675 | G | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-516G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044675 | |||||||
| chr19:47044676 | A | G | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-515A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044676 | |||||||
| chr19:47044716 | T | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-475T>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044716 | |||||||
| chr19:47044768 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1313-423G>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044768 | |||||||
| chr19:47044839 | G | C | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-352G>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044839 | |||||||
| chr19:47044903 | A | G | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-288A>G | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47044903 | |||||||
| chr19:47045011 | C | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-180C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045011 | |||||||
| chr19:47045031 | C | A | 378 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(375): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1313-160C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045031 | |||||||
| chr19:47045036 | AAACAAAA others(18): Show |
A | 2 | a0001c0013t0001g0313 a0004c0015t0001g0410 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-152_1313-128d others(27): Show |
NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr19 | 47045036 | ||||||
| chr19:47045039 | C | A | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1313-152C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045039 | |||||||
| chr19:47045046 | C | A | 1 | a0001c0002t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1313-145C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045046 | |||||||
| chr19:47045052 | C | A | 2 | a0001c0002t0001g0111 a0001c0002t0001g0271 |
2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1313-139C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045052 | |||||||
| chr19:47045057 | C | A | 1 | a0001c0002t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1313-134C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045057 | |||||||
| chr19:47045061 | C | A | 1 | a0001c0002t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1313-130C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045061 | |||||||
| chr19:47045065 | C | A | 3 | a0001c0002t0001g0271 a0001c0013t0001g0313 a0004c0015t0001g0410 |
3 | HG02109.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-126C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045065 | |||||||
| chr19:47045069 | A | C | 165 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0012 others(162): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.1313-122A>C | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045069 | |||||||
| chr19:47045069 | A | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(208): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1313-122A>T | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045069 | |||||||
| chr19:47045077 | C | A | 4 | a0001c0002t0001g0111 a0001c0002t0001g0271 a0001c0013t0001g0313 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-114C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045077 | |||||||
| chr19:47045164 | C | A | 1 | a0001c0001t0001g0406 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1313-27C>A | NPAS1 | ENSG00000130751.10 | transcript | ENST00000602212.6 | protein_coding | 11/11 | chr19 | 47045164 |